Abstract
Transcription factors play a determining role in lineage commitment and cell differentiation. Interferon regulatory factor 8 (IRF8), a hematopoietic transcription factor, is prominently upregulated in dendritic cells (DC) by autoactivation and controls DC differentiation and function. However, it is unclear how IRF8 autoactivation is controlled and eventually limited. Here we identified a novel long non-coding RNA transcribed from the +32 kb enhancer downstream of IRF8 transcription start site and expressed specifically in plasmacytoid DC (pDC), referred to as lncIRF8. A sequence element of the lncIRF8 promoter, but not lncIRF8 itself, is crucial for pDC and classical DC type 1 (cDC1) differentiation. In DC development IRF8 autoactivation is first initiated by flanking enhancers and then second controlled by feedback inhibition through the lncIRF8 promoter element in the +32 kb enhancer. Our work reveals a previously unrecognized negative feedback loop of IRF8 that orchestrates its own expression and thereby controls DC differentiation.
Introduction
Lineage-determining transcription factors (TF) are master regulators of gene programs that frequently initiate self-reinforcing loops by autoactivation. TF autoactivation is important for cells to pass restriction points during development (referred to as points of no return) and to enforce cellular identity. Molecular circuitries of autoactivation have been studied for several TF, such as GATA-binding factor 1 (GATA1), PU.1 (encoded by Spi1), CCAAT enhancer-binding protein α and ε (C/EBPα and ε) (Graf and Enver, 2009; Loughran et al., 2020; Nishimura et al., 2000; Okuno et al., 2005; Theilgaard-Mönch et al., 2022). A further example is interferon regulatory factor 8 (IRF8), which shows autoactivation in cooperation with basic leucine zipper ATF-like transcription factor 3 (Batf3) (Anderson et al., 2021; Grajales-Reyes et al., 2015). An important principle in nature is negative feedback control to avoid signal overshooting and toxicity. Negative feedback control applies also to lineage-determining TF, however there is a paucity on our knowledge of the molecular mechanisms involved.
IRF8 is a hematopoietic TF positioned at the center of the regulatory gene network for dendritic cell (DC) development (Anderson et al., 2021; Chauvistré and Seré, 2020; Lin et al., 2015; Nutt and Chopin, 2020; Tamura et al., 2015; Verlander et al., 2022). IRF8 knockout mice show abnormal development of classical DC type 1 (cDC1) and plasmacytoid DC (pDC) (Durai et al., 2019; Schiavoni et al., 2002; Sichien et al., 2016; Tsujimura et al., 2003). IRF8 is prominently upregulated during DC development by autoactivation (Grajales-Reyes et al., 2015; Lin et al., 2015), yet how IRF8 autoactivation is controlled and eventually limited, and the epigenetic mechanisms involved is largely unknown.
IRF8 expression in hematopoietic cells is induced and maintained by enhancers located at -50 kb, +32 kb, +41 kb and +56 kb relative to IRF8 transcription start site (TSS) (Anderson et al., 2021; Bagadia et al., 2019; Durai et al., 2019; Grajales-Reyes et al., 2015; Murakami et al., 2021; Schönheit et al., 2013). Enhancers regulate complex gene networks and can also produce non-coding RNA, referred to as enhancer RNA (eRNA). eRNA serve as an indicator for enhancer activity and some eRNA have an activity on their own and act in cis or trans to regulate cell fate decisions (Sartorelli and Lauberth, 2020; Statello et al., 2021). Enhancer-associated long non-coding RNA (lncRNA) represent a class of lncRNA transcribed from active enhancers. Thus, eRNA and enhancer-associated lncRNA provide opportunities to detect enhancer activity and to investigate enhancer function.
DC are highly specialized immune cells that play a critical role in regulating innate and adaptive immune responses (Cabeza-Cabrerizo et al., 2021). DC develop from hematopoietic stem cells (HSC) via successive steps of lineage commitment and differentiation. More specifically, HSC develop into multipotent progenitors (MPP) that are committed to DC restricted common DC progenitors (CDP) and differentiate into classic DC (cDC) type 1 and type 2 (cDC1 and cDC2, respectively) and pDC (Anderson et al., 2021; Cabeza-Cabrerizo et al., 2021; Nutt and Chopin, 2020; Rodrigues and Tussiwand, 2020). pDC were recently also shown to develop from lymphoid progenitors (Dress et al., 2019; Rodrigues et al., 2018; Rodrigues and Tussiwand, 2020). Differential expression of IRF8 regulates DC and monocyte specification in a dose-dependent manner (Cytlak et al., 2020; Murakami et al., 2021). IRF8 expression starts at the CDP stage, and is high in pDC and cDC1, which is attributed to the autoactivation of IRF8 during DC subsets specification (Grajales-Reyes et al., 2015; Lin et al., 2015). Interestingly, IRF8 can act as a transcriptional activator or repressor in hematopoiesis by interacting with different partner TF and binding to specific DNA sequences (Tamura et al., 2015).
As an activator, IRF8 binds to its own promoter in DC differentiation, which is considered as the autoactivation capacity of IRF8 (Grajales-Reyes et al., 2015; Lin et al., 2015). For instance, IRF8 interacts with partner TF, such as PU.1, to initiate IRF8 autoactivation at the CDP stage (Grajales-Reyes et al., 2015). Inversely, IRF8 inhibits C/EBPα activity in neutrophil differentiation (Kurotaki et al., 2014). IRF8 also represses C/EBPβ to generate and maintain DC lineage-specific enhancer landscapes (Bornstein et al., 2014). In addition, IRF8 is important for the Myc-Mycl transition in DC differentiation (Anderson III et al., 2021). IRF8 represses Myc expression in progenitors, while IRF8 at high levels interacts with PU.1 and drives Mycl expression (Anderson III et al., 2021). All this emphasizes the central position of IRF8 in coordinating the gene network that regulates DC differentiation and function.
During DC differentiation, the IRF8 gene locus shows high epigenetic dynamics, including histone modifications and TF binding identified by ChIP-seq (Chauvistré and Seré, 2020; Durai et al., 2019; Grajales-Reyes et al., 2015; Lin et al., 2015), chromatin accessibility measured by ATAC-seq (Kurotaki et al., 2019; Li et al., 2019), and three-dimensional chromatin structure remodeling determined by chromosome conformation capture (3C) (Schönheit et al., 2013). All this emphasizes the impact of epigenetic regulators on IRF8 gene activity in DC differentiation. Notably, IRF8 is flanked by multiple enhancers at -50 kb, +32 kb, +41 kb and +56 kb that regulate IRF8 expression in hematopoietic cells (Anderson et al., 2021; Murakami et al., 2021). These four enhancers were found to be driven by PU.1, Batf3, E proteins and Runt-related transcription factor (RUNX)-core binding factor beta (CBFβ) (RUNX-CBFβ), respectively (Bagadia et al., 2019; Durai et al., 2019; Grajales-Reyes et al., 2015; Murakami et al., 2021; Schönheit et al., 2013).
Chromatin conformation, particularly enhancer-promoter interactions, provides a platform for TF-driven gene regulation and serves as a driving force for cell-fate determinations (Misteli and Finn, 2021; Oudelaar and Higgs, 2021; Stadhouders et al., 2019). Schönheit et al. demonstrated IRF8 promoter interactions with its upstream enhancers by quantitative 3C (Schönheit et al., 2013). In this study PU.1 was found to regulate chromatin remodeling between the -50 kb enhancer and the IRF8 promoter in myeloid differentiation. Thus, while the Schönheit et al., 2013 study represents a good starting point, it has remained of great importance to unveil the physical chromatin interactions of the IRF8 promoter with upstream and downstream enhancers on a large scale and at high resolution to understand IRF8 regulation during DC differentiation (Murakami et al., 2021).
Frequently, chromatin data, including ATAC-seq and/or ChIP-seq data, are used to identify regulatory elements of gene transcription. Here we embarked on a different approach and searched for lncRNA, which by themselves might have regulatory functions or are indicative of enhancer activity. We identified a novel lncRNA transcribed from the IRF8 +32 kb enhancer, which is specifically expressed in pDC, referred to as lncIRF8. We found that the lncIRF8 promoter element but not lncIRF8 itself impacts pDC and cDC1 development. Thus, lncIRF8 acts as an indicator for the IRF8 +32 kb enhancer activity. Importantly, our study revealed a previously unrecognized negative feedback loop of IRF8 in DC differentiation. IRF8 first activates its expression by autoactivation via the +32 kb enhancer and second limits its own expression through the lncIRF8 promoter element in the +32 kb enhancer.
Results
lncIRF8 marks a pDC specific IRF8 enhancer element
IRF8 expression in DC development is subject to complex epigenetic regulation. Here we used an integrated approach with RNA-seq, ATAC-seq, ChIP-seq and Capture-C to track the dynamics of gene expression, histone modification and chromatin conformation in the sequel MPP, CDP, pDC, cDC1 and cDC2 (Figure 1, Figure S1 and Figure S2A).
We performed de-novo transcript assembly of the RNA-seq data and detected two previously unknown transcripts without coding potential downstream of IRF8: a pDC specific lncRNA (TCONS_00190250) in the following referred to as lncIRF8 and a cDC1 specific lncRNA (TCONS_00190258; Figure 1A and Figure S1). lncIRF8 is transcribed within an enhancer region located 32 kb downstream of the IRF8 TSS labeled by H3K27ac and H3K4me1 and occupied by DC differentiation-associated TF, such as IRF8 and PU.1 (Figure 1A and Figure S1). This region is largely devoid of H3K9me3, a chromatin modification frequently associated with heterochromatin, indicating an open chromatin configuration in DC (Figure S1). In addition, sequences of this region have been implicated in DC development and referred +32 kb enhancer (Durai et al., 2019). Thus, we proceeded to study lncIRF8 in detail.
ATAC-seq analysis revealed further details of the lncIRF8 region in CDP, pDC, cDC1 and cDC2 (Figure 1A, Figure 2A and Figure S1). In cDC1 the prominent ATAC-seq and IRF8 peaks mark the cDC1 specific +32 kb enhancer (Durai et al., 2019). In pDC the ATAC-seq peak is smaller and shifted further towards downstream but aligns well with the valley in the prominent H3K27ac peak. This ATAC-seq peak marks the lncIRF8 promoter and aligns with p300 and H3K4me3 (Figure 2A and Figure S1) (Durai et al., 2019). All this indicates that this chromatin region is open and transcriptionally active in pDC, enabling lncIRF8 transcription.
Next, we determined the chromatin conformation of the IRF8 locus and the lncIRF8 region. We generated interaction profiles by nuclear-titrated (NuTi) Capture-C in MPP, CDP, pDC, cDC1 and cDC2 (Figure S2A and B) using IRF8 promoter as viewpoint. The IRF8 promoter shows multiple interactions with regions spanning up to ∼100 kb upstream and downstream of IRF8 (Figure 1B and Figure S1). In pDC the IRF8 promoter interactions are stronger with the upstream sequences than with downstream sequences (Figure 1C and Figure S2C). In cDC1 IRF8 promoter interactions are more confined to the regions downstream of IRF8 compared to MPP, CDP and pDC (Figure 1C, Figure S2C). This suggests that upstream and downstream sequences of IRF8 gene are involved in differentially regulating IRF8 expression and controlling the development of pDC and cDC1, respectively.
The CCCTC-binding factor (CTCF) is important for regulation of chromatin conformation through loop extrusion (Sanborn et al., 2015) and we therefore visualized CTCF binding sites in the IRF8 locus in DC (Garber et al., 2012). Interestingly, most of the IRF8 flanking enhancers (Durai et al., 2019; Grajales-Reyes et al., 2015; Murakami et al., 2021; Schönheit et al., 2013) are located within convergent CTCF binding sites upstream and downstream of the IRF8 gene (Figure 1B and Figure S1). There are also multiple interactions within this region without convergent CTCF binding sites, suggesting interactions with IRF8 promoter in a CTCF independent manner, such as by TF binding, active histone modifications and gene transcription (Figure 1B and Figure S1) (Owens et al., 2022).
Surprisingly, in pDC H3K27ac at the lncIRF8 promoter is high, but this locus shows less interactions with the IRF8 promoter in pDC compared to CDP, cDC1 and cDC2 (Figure 1C and Figure S2C). In addition, in pDC the IRF8 protein occupancy at the lncIRF8 promoter is low and much higher in cDC (Figure 1A and Figure S1) (Durai et al., 2019; Grajales-Reyes et al., 2015). These observations warrant further studies and we thus proceeded to investigate the lncIRF8 locus in detail.
lncIRF8 promoter KO compromises pDC and cDC1 development
First, we annotated lncIRF8. Our de-novo transcript assembly of RNA-seq data revealed different isoforms of lncIRF8, with the most prominent isoform comprising exon 2 and 3 (Figure 1A, Figure 2A and Figure S1). Additionally, 3’ end and 5’ end RACE PCR confirmed the anatomy of this lncIRF8 isoform: two exons, one intron, and a polyA tail (Figure 2A). Then second, we deleted 300 bp in the lncIRF8 promoter by CRISPR/Cas9 editing in conditionally immortalized HoxB8 MPP (Figure 2A and Figure S3A-D). The lncIRF8 promoter is located in the IRF8 +32 kb enhancer region and is in close proximity to the cDC1 specific +32 kb enhancer (Durai et al., 2019) (Figure 2A and Figure S4). The 300 bp deletion comprises the H3K4me3 promoter mark and is confined to open chromatin identified by ATAC-seq and positioned in the valley of the H3K27ac mark (Figure 2A). Additionally, it contains binding sites for IRF8, PU.1, and Batf3 TF, which are important for DC development (Figure 2A and Figure S4B).
Generation of a precise deletion requires clonal cell populations, which is hardly achieved in somatic cells due to their limited life span. Therefore, we developed a Mx-Cas9-GFP system of conditionally immortalized HoxB8 MPP, which upon differentiation faithfully recapitulate DC development (Figure S3A and B) (Xu et al., 2021). HoxB8 MPP were obtained from bone marrow of Mx-Cas9-GFP mice by infection with the estrogen (E2) inducible HoxB8-ER. These HoxB9 MPP exhibited an extended lifespan and robust clonogenic potential and differentiated into all DC subsets in vitro and in vivo (Xu et al., 2021). Infection of gRNA targeting lncIRF8 promoter in Mx-Cas9-GFP HoxB8 MPP and induction of Cas9 by interferon generated single-cell lncIRF8 promoter KO clones. Five out of 71 single-cell colonies with homozygous deletions were further studied and subjected to DC differentiation (Figure 2C-E, Figure S3C-G, Figure S5A-I).
lncIRF8-promoter KO abolished lncIRF8 expression during DC differentiation compared to control without deletion (Figure 2B). Surprisingly, IRF8 expression was also severely compromised, which points to a cross-talk of the lncIRF8 promoter element with the IRF8 promoter. To determine whether lncIRF8-promoter KO also impacts DC subsets, CD11c+ DC, pDC and cDC subsets cDC1 and cDC2 were analyzed (Figure 2C and Figure S3E-G). Frequencies of pDC and cDC1 were severely reduced, while cDC2 were unaffected (Figure 2C). Accordingly, lncIRF8-promoter KO cultures contained mainly cDC2 and some undifferentiated cells and were more homogenous compared to control without deletion, which contain multiple DC subsets (Figure 2C and D, Figure S3F).
lncIRF8-promoter KO affected also the differentiation propensity of progenitors upon E2 withdrawal from MPP/CDP culture (Figure S2A and Figure S5A-I). lncIRF8-promoter KO showed a marked increase in strongly adhesive cells compared to control (Figure S5B). lncIRF8-promoter KO cultures had higher frequencies of Gr1+ monocytes (Figure 2E, Figure S5H and I) and lower frequencies of all DC subsets CD11c+ DC, pDC, cDC1, and cDC2 (Figure S5C-G) compared to control without deletion.
We then investigated the impacts of lncIRF8 promoter KO on DC differentiation in vivo and transplanted CD45.2 lncIRF8-promoter KO and CD45.2 control HoxB8 MPP into irradiated CD45.1 recipient mice (Figure S5J). DC in bone marrow and spleen were analyzed by flow cytometry on day 7 and 14 after cell transplantation (Figure 3, Figure S5J and K).
In bone marrow, lncIRF8-promoter KO cells mostly differentiated into Gr1+ monocytes, and lower frequencies of all DC subsets were observed on day 7 for lncIRF8-promoter KO cells compared to control (Figure 3A-F). In spleen, frequencies of cell populations from lncIRF8-promoter KO and control were similar to bone marrow, including lower frequencies of all DC subsets for lncIRF8-promoter KO (Figure 3G-L). CD45.2 donor HoxB8 cells were largely lost at day 14 after cell transplantation (Figure 3B-F and Figure 3H-L). Thus, lncIRF8 promoter KO compromised pDC and cDC1 development both in vitro and in vivo.
lncIRF8 acts as an indicator of IRF8 +32 kb enhancer activity in pDC
Knockout of lncIRF8 promoter and thus abolishment of lncIRF8 expression severely diminished pDC and cDC1 development in vitro and in vivo. The lncIRF8 promoter is located within IRF8 +32 kb enhancer (Durai et al., 2019) and thus it was important to determine whether lncIRF8 itself plays a role in regulating pDC and cDC1 development. To address this question, we (i) overexpressed lncIRF8 in wild-type MPP and (ii) re-expressed lncIRF8 in lncIRF8-promoter KO MPP and monitored its impact on DC development (Figure 4 and Figure S6).
lncIRF8 cDNA was cloned into a polyA lentivirus vector. An “AATAAA” stop signal (Alvarez-Dominguez et al., 2015) was inserted at the 3’ end of lncIRF8 to avoid longer transcripts than lncIRF8 (plncIRF8-pA, Figure 4B). The respective pGFP-pA vector was used as control. lncIRF8 overexpressing single-cell clones were generated by limiting dilution (Figure S6A), expanded and subjected to DC differentiation. As expected lncIRF8 expression was markedly increased in plncIRF8-pA infected cells compared to control, while there were no significant differences in IRF8 expression between the two groups during DC differentiation (Figure 4C). Further, there were no differences in the frequencies of pDC, cDC1, and cDC2 between plncIRF8-pA infected cells and controls (Figure 4D and E, Figure S6B-D), indicating that lncIRF8 overexpression has no effect on IRF8 expression and DC differentiation.
To further extend this observation we performed a lncIRF8 rescue in lncIRF8 promoter KO MPP. lncIRF8 was re-expressed in lncIRF8-promoter KO MPP by lentiviral vector and cells were subjected to DC differentiation (Figure S6E). lncIRF8 RNA was effectively expressed and cells differentiated in response to Flt3L (Figure S6F). Yet frequencies of pDC and cDC1 were very low to absent and not rescued by lncIRF8 expression (Figure S6G and H).
In a nutshell, lncIRF8 overexpression and rescue had no effects on pDC and cDC1 development. This strongly suggests that lncIRF8 has no activity on its own in DC differentiation but rather acts as an indicator for the activation state of sequences within the IRF8 +32 kb enhancer. In addition, the lncIRF8 promoter comprises a sequence element with impact on pDC and cDC1 development.
Activation of lncIRF8 promoter promotes cDC1 development
Next, we proceeded to study the impact of the sequence element within lncIRF8 promoter on IRF8 expression and DC differentiation using CRISPR activation by dCas9-VP64 (Figure 5A). dCas9-VP64 is a mutated Cas9 deficient in nuclease activity, which is fused to the VP64 effector domain and confers gene activation. Targeting of dCas9-VP64 to the lncIRF8 promoter was achieved with specific gRNAs (Figure S7I). We also included targeting dCas9-VP64 to the IRF8 promoter to study the interplay with the lncIRF8 promoter. FACS sorted HoxB8 MPP expressing dCas9-VP64 and gRNA were subjected to DC differentiation (Figure S7A) and analyzed for lncIRF8 and IRF8 expression and DC subset composition (Figure 5B-E).
Activation of the lncIRF8 promoter by dCas9-VP64 caused a massive increase of lncIRF8 expression at DC differentiation day 0 (Figure 5C). The activation of the lncIRF8 promoter led also to IRF8 upregulations at DC differentiation day 5, 7, and 9 compared to non-targeting control (Figure 5A and C). This demonstrates the positive impact of the lncIRF8 promoter element on IRF8 expression during DC differentiation and is in accord with the physical interaction of lncIRF8 and IRF8 promoters by Capture-C (Figure 1B and Figure S1).
Intriguingly, in lncIRF8-VP64 cells lncIRF8 expression was downregulated at DC differentiation day 5, 7 and 9, while IRF8 expression was upregulated (Figure 5C). This indicates a repressive effect of IRF8 on lncIRF8 promoter and is in accord with IRF8 binding to the lncIRF8 region by ChIP-seq (Figure 1 and Figure S1). This observation suggests a negative feedback loop of IRF8 on the lncIRF8 promoter during DC differentiation (Figure 5C).
Activation of IRF8 promoter by dCas9-VP64 increased IRF8 expression at DC differentiation day 0, 5, 7, and 9, while expression of lncIRF8 was unaffected compared to non-targeting control (Figure 5A and C). As expected IRF8 promoter activation led to higher pDC frequencies (Figure 5B and D), and also increased cDC1 frequencies compared to the non-targeting controls (Figure 5B and E). Importantly, lncIRF8 promoter activation by dCas9-VP64 also increased cDC1 frequencies and this was particularnprominent at day 9 of DC differentiation (Figure 5B and E). Frequencies of cDC2 were decreased at day 9 and other populations, including pDC, remained unchanged (Figure 5B and D, Figure S7C-E).
Taken together our CRISPR activation of the lncIRF8 and IRF8 promoters by dCas9-VP64 suggest a negative feedback loop of IRF8 for pDC and cDC1 development.
Negative feedback regulation of lncIRF8 and IRF8 promoters controls DC differentiation
To directly investigate the negative feedback loop of IRF8 regulation, we repressed lncIRF8 and IRF8 promoters by targeted repression with dCas9-KRAB and analyzed the DC subsets during DC differentiation (Figure 6A-F). dCas9-KRAB is a nuclease deficient Cas9 fused to the KRAB effector domain, which confers gene repression when positioned with specific gRNA (Figure S7I).
Targeted repression of the IRF8 promoter decreased IRF8 expression as expected but massively increased lncIRF8 expression compared to non-targeting control (Figure 6A and C). This is very much in line with IRF8 impacting lncIRF8 expression by a negative feedback loop. Positioning the dCas9-KRAB repressor in the IncIRF8 promoter led to downregulation of both IRF8 and lncIRF8 expression, which confirms the lncIRF8 promoter element acting on the IRF8 promoter (Figure 6A and C).
Interestingly, targeted repression of the IRF8 promoter severely compromised development of all DC subsets, including pDC, cDC1 and cDC2, compared to non-targeting controls and yielded CD11c+ cells with progenitor-like spherical morphology (Figure 6B, D-F, Figure S7F-H). This reemphasizes the pivotal role of IRF8 for DC development known from studies on IRF8 knockout mice (Murakami et al., 2021; Schiavoni et al., 2002; Sichien et al., 2016; Tsujimura et al., 2003). In addition, targeted repression of the lncIRF8 promoter (lncIRF8-KRAB) also compromised pDC and cDC1 development (Figure 6B, D and E). This result is very similar to the lncIRF8 promoter KO analyzed above (Figure 2A-C).
All these findings support a model of IRF8 regulating its own expression by a negative feedback loop acting on the IRF8 +32 kb enhancer to limit IRF8 autoactivation (Figure 7). This regulatory IRF8 +32 kb enhancer element is marked by lncIRF8. IRF8 expression starts in CDP and further increases in pDC and cDC1, with particularly high expression in pDC (Figure 1A and Figure S1). The increase in IRF8 expression is proposed to be due to an increase in the interactions of the IRF8 promoter with upstream and downstream sequences. In pDC the IRF8 promoter-enhancer interactions are more with upstream chromatin regions (Figure 1C), which relates to high IRF8 expression. In cDC1 the IRF8 promoter interactions are stronger with the regions downstream of IRF8 (Figure 1C) and the IRF8 +32 kb enhancer marked by lncIRF8 confers transcriptional repression.
In our model we propose an IRF8 repressor complex that differentially acts on the IRF8 +32 kb enhancer element in a DC subset specific manner to limit IRF8 autoactivation. In cDC1 the +32 kb enhancer is repressed by the IRF8 repressor complex through negative feedback inhibition (prominent IRF8 binding in cDC by ChIP-seq; Figure 7A), which limits IRF8 autoactivation and expression. Conversely, in pDC there is less IRF8 repressor complex binding to the +32 kb enhancer, which results in high IRF8 and lncIRF8 transcription (Figures 7A). Recapitulating the IRF8 repressor complex with dCas9-KRAB and targeting lncIRF8 promoter in the +32 kb enhancer reduced IRF8 expression (Figure 7B). Conversely, activation of the +32 kb enhancer boosted lncIRF8 and IRF8 expression (Figure 7B). Thus, an intricate feedback loop of IRF8 on the +32 kb enhancer orchestrates IRF8 expression and thus DC differentiation.
Discussion
Hematopoiesis is a particularly well studied stem cell system and therefore provides an excellent model for studying TF in lineage commitment and cell differentiation, and the molecular principles involved (Graf and Enver, 2009; Laurenti and Göttgens, 2018; Nutt and Chopin, 2020). This work revealed a previously unrecognized negative feedback loop of IRF8 in DC differentiation and shows how IRF8 autoactivation is controlled and ultimately limited. IRF8 is crucial for DC lineage specification both in humans and mice (Anderson et al., 2021; Cabeza-Cabrerizo et al., 2021; Cytlak et al., 2020; Kurotaki et al., 2019; Nutt and Chopin, 2020). IRF8 is upregulated by autoactivation via the +32 kb enhancer (Grajales-Reyes et al., 2015; Lin et al., 2015). However, how IRF8 expression is controlled at late stages of DC differentiation and eventually limited is not known. Here we demonstrate that IRF8 expression is limited by a negative feedback loop via a sequence element marked by lncIRF8 in the IRF8 +32 kb enhancer.
IRF8 expression in hematopoiesis is regulated by its flanking enhancers, which determine lineage specification and DC subset development (Bagadia et al., 2019; Durai et al., 2019; Grajales-Reyes et al., 2015; Murakami et al., 2021; Schönheit et al., 2013). Frequently, enhancers are identified by ATAC-seq and ChIP-seq (Durai et al., 2019; Murakami et al., 2021), and here we embarked on a different approach and searched for eRNA and enhancer-associated lncRNA by RNA-seq. We identified a novel pDC specific lncRNA (lncIRF8) transcribed from the IRF8 +32 kb enhancer. lncIRF8 itself lacks activities in DC differentiation but a lncIRF8 promoter element is crucial for pDC and cDC1 development. Upon deletion of this lncIRF8 promoter element pDC and cDC1 development was severely compromised, demonstrating that this sequence is important for both pDC and cDC1 development.
We propose a model where IRF8 expression during DC differentiation is in a first step initiated and activated through flanking enhancers, including the +32 kb enhancer by autoactivation (Grajales-Reyes et al., 2015; Lin et al., 2015) (Figure 7). In a second step the lncIRF8 promoter element confers feedback inhibition, which limits IRF8 expression. This feedback inhibition is different for pDC and cDC1, both of which express high levels of IRF8 (Bornstein et al., 2014; Grajales-Reyes et al., 2015; Lin et al., 2015). In cDC1, IRF8 expression is attributed to IRF8 autoactivation through the +32 kb enhancer driven by the Batf3-IRF8 complex (Durai et al., 2019; Grajales-Reyes et al., 2015). In pDC, IRF8 expression is even higher than in cDC1 (Bornstein et al., 2014; Lin et al., 2015), which we propose is due to less feedback inhibition at late stages of DC differentiation.
A candidate for mediating IRF8 feedback inhibition is IRF8 itself, since IRF8 works as transcriptional activator or repressor, depending on context. IRF8 activator or repressor function depends largely on the heterodimers (or even heterotrimers) with partner TF that bind to specific DNA sequences (Chang et al., 2018; Huang et al., 2016; Humblin et al., 2017; Tamura et al., 2015; Yoon et al., 2014). Modifications on IRF8 protein, such as phosphorylation and small molecule conjugation, also alter IRF8 activity (Chang et al., 2012; Konieczna et al., 2008). Potential IRF8 heterodimer partners, to form repressor complexes, are ETV6 or IRF2 (Huang et al., 2016; Humblin et al., 2017; Lau et al., 2018).
The IRF8 repressor complex is proposed to bind to the +32 kb enhancer in cDC but not in pDC. This notion is in line with a prominent IRF8 signal at the +32 kb enhancer in cDC, which is absent in pDC (Durai et al., 2019; Grajales-Reyes et al., 2015) (Figure 1A, Figure S1, Figure S4A and Figure 7A).
Further support of our model stems from our CRIPSR activation/interference experiments (Figure 7B). CRIPSR activation of IRF8 promoter by dCas9-VP64 mimics IRF8 up-regulation during DC differentiation and causes an increase in pDC and cDC1 (Figure 5). CRIPSR interference of lncIRF8 promoter by dCas9-KRAB recapitulates transcriptional repressor binding to the +32 kb enhancer and causes IRF8 promoter inhibition (Figure 6).
We extended our study to delineate the chromatin conformation of the IRF8 promoter with flanking sequences by Capture-C. The IRF8 promoter was found to interact with its flanking enhancers already at the CDP stage and then interactions with specific upstream and downstream sequences are proposed to guide pDC and cDC specification, respectively. This is in accord with previous studies where some of these IRF8 flanking enhancers were required to maintain high levels of IRF8 expression (Anderson et al., 2021; Murakami et al., 2021).
We demonstrate that deletion of the lncIRF8 promoter element severely decreased IRF8 expression and abolished both pDC and cDC1 development in vitro and in vivo upon cell transplantation. These results are very similar to a previous study on cDC1 specific +32 kb enhancer knockout mice, which demonstrates the impact of +32 kb enhancer for cDC1 development in vivo (Durai et al., 2019). The lncIRF8 promoter is located in close proximity to the cDC1 specific +32 kb enhancer and thus can be expected to have overlapping functions. However, CRISPR deletion and interference of lncIRF8 promoter compromised both cDC1 and pDC development, while the +32 kb enhancer knockout in mice affected only cDC1 development. The reason for this discrepancy is not clear and could be due to genetic compensation for pDC development in +32 kb enhancer KO mice. Alternatively, the lncIRF8 promoter element might have additional functions for pDC development, which need to be further addressed.
eRNA and enhancer-associated lncRNA are indicative of enhancer activity, however whether the process of their transcription, the transcripts themselves, or both are functionally linked to enhancer activity, remains unclear (Sartorelli and Lauberth, 2020; Statello et al., 2021). Previous studies revealed that some eRNA and enhancer-associated lncRNA are indeed functionally connected with expression of the respective target genes (Sartorelli and Lauberth, 2020; Statello et al., 2021). Here we found no apparent activity of lncIRF8 on its own in pDC and cDC1 development, as demonstrated by lncIRF8 overexpression and rescue experiments. Thus, lncIRF8 appears to rather serve as an indicator for IRF8 +32 kb enhancer activity.
In conclusion, by analyzing the gene expression and epigenetic profiles of the IRF8 locus, we identified an enhancer element marked by lncIRF8 that regulates IRF8 and controls DC differentiation through a negative feedback loop. Our results suggest that IRF8 regulates itself by its flanking enhancers in DC fate determination: First, IRF8 induces its expression by autoactivation via flanking enhancers, including the IRF8 +32 kb enhancer, to initiate DC differentiation, and second limits its expression at late stages via the lncIRF8 promoter element within the same +32 kb enhancer by feedback inhibition. This molecular principle of feedback inhibition is expected to also apply to other TF and cell differentiation systems.
Author Contributions
H.X. and M.Z. conceived the study. H.X. and K.G. performed the Capture-C and data analysis. Z.L., C.C.K., T.L., and I.G.C. did ATAC-seq, ChIP-seq, RNA-seq and data analysis. H.X., K.G., M.A.S.T.,
T.L. and K.S. performed molecular cloning, cell culture and mouse experiments. H.X. and M.Z. wrote the manuscript and further edited upon input from all co-authors.
Declaration of Interests
The authors declare no competing interests.
Materials and Methods
Resource Table
Data and code availability
ATAC-seq (MPP, CDP and cDC2), Capture-C targeting IRF8 promoter (MPP, CDP, cDC1, cDC2 and pDC), IRF8 ChIP-seq (cDC and pDC), and RNA-seq (MPP, CDP, cDC1, cDC2 and pDC) data generated in this study have been deposited in Gene Expression Omnibus and are accessible through GEO Series accession numbers GSE198651.
ATAC-seq data of cDC1 and pDC (GSE118221) are published (Li et al., 2019), and the ATAC-seq data of MPP, CDP and cDC2 of the same study are described here (GSE198651). ChIP-seq of CTCF in DC (GSE36099) (Garber et al., 2012), H3K27ac (GSE73143) (Allhoff et al., 2016), H3K4me1 and PU.1 (GSE57563) (Allhoff et al., 2014), H3K4me3 and H3K9me3 (GSE64767) (Lin et al., 2015) in MPP, CDP, cDC and pDC were re-analyzed in this study.
The sequence of the pDC specific lncRNA (lncIRF8 identified by RACE PCR) and the cDC1 specific lncRNA (TCONS_00190258 identified by RNA-seq) has been submitted to GenBank. The GenBank accession numbers for lncIRF8 and TCONS_00190258 are ON134061 and ON134062, respectively.
Animals
Wild type C57BL/6, Mx-Cas9-GFP knock-in mice (Kühn et al., 1995; Platt et al., 2014; Xu et al., 2021), and CD45.1 recipient C57BL/6 mice were used in this study. Mice were kept under specific pathogen-free conditions in the central animal facility of RWTH Aachen University Hospital, Aachen, Germany. All the animal experiments were approved by the local authorities of the German State North Rhine-Westphalia, Germany according to the German animal protection law.
Cell lines and culture
Multipotent progenitors (MPP) were obtained from mouse bone marrow and expanded in vitro with a two-step protocol as described in (Felker et al., 2010). Conditionally immortalized HoxB8 MPP were generated by retrovirus infection of bone marrow cells from wild-type or Mx-Cas9-GFP knock-in mice with an estrogen (E2) inducible HoxB8 estrogen receptor (ER) fusion gene (HoxB8-ER) (Redecke et al., 2013; Xu et al., 2021). MPP were grown in RPMI 1640 medium with 10% FCS (Gibco, 10270106), 100 U/ml penicillin/streptomycin, 2 mM L-glutamine and 50 μM β-ME with a four-cytokine cocktail of SCF, Flt3 ligand (Flt3L), IGF-1, and IL-6/soluble IL-6 receptor fusion protein (hyper-IL-6) as before (referred to as MPP growth medium) (Felker et al., 2010; Xu et al., 2021). E2 (1 µM) was added to activate HoxB8-ER and to maintain the conditionally immortalized state of HoxB8 MPP. Cell density was adjusted to 1.5 million cells/ml every day. HEK293T cells for retrovirus and lentivirus production were grown in DMEM supplemented with 10% FCS (PAA, A01125-499), 100 U/ml penicillin/streptomycin, 2 mM L-glutamine.
Methods Details
In vitro DC differentiation with HoxB8 MPP
HoxB8 MPP were differentiated into DC using a two-step protocol modified from (Felker et al., 2010) and described in (Xu et al., 2021). In brief, 0.75 million cells/ml were grown in MPP growth medium with 50 ng/ml Flt3L (Peprotech, 300-19) and reduced E2 (0.01 μM) for two days and cell density was kept to 0.75 million cells/ml. To induce DC differentiation, HoxB8 MPP were then washed with PBS to remove cytokines and E2, and cultured in RPMI 1640 medium supplemented with FCS, penicillin/streptomycin, L-glutamine, β-ME (same concentrations as above), and Flt3L (50 ng/ml, Peprotech) (referred to as DC differentiation day 0). Partial medium changes were performed on differentiation day 3 and 6. Spontaneous DC differentiation of HoxB8 MPP was achieved simply by removing E2 from growth medium (SCF, Flt3L, IGF1 and hyper-IL6), and culturing the cells at 1.5 million cells/ml (Xu et al., 2021).
Nuclear-Titrated (NuTi) Capture-C
Wild-type bone marrow cell-derived MPP, CDP, cDC1, cDC2, and pDC were generated in vitro with the two-step protocol as described in (Felker et al., 2010). Cell populations were sorted by BD FACSAria IIu or BD FACSMelody, MPP are Gr1- CD117hi CD135low/-, CDP are Gr1- CD117int CD135+ CD115+, cDC1 are CD11c+ CD11blow/- XCR1+, cDC2 are CD11c+ CD11b+ XCR1-, pDC are CD11c+ CD11b- B220+.
The chromatin conformation capture (3C) library preparation protocol used in this study was modified from (Downes et al., 2021; Downes et al., 2022). MPP, CDP, cDC1, cDC2 and pDC were fixed with formaldehyde (final concentration 2%) and subjected to nuclear isolation according to the protocol in (Downes et al., 2022; Li et al., 2019). Nuclei (15-20 million per sample) were digested with DpnII and DNA fragments were ligated by T4 DNA HC ligase. DNA was extracted and purified with Phenol-Chloroform-Isoamyl alcohol (PCI, 25:24:1). DpnII digestion efficiency was determined by SYBR qPCR with the primers listed in Resource Table and the quality of 3C libraries was investigated by agarose gel (1%) electrophoresis; 3C samples were used only if the DpnII digestion efficiency was more than 70%.
For IRF8 promoter viewpoint 2 oligonucleotide probes targeting IRF8 promoter were designed with the design tool Oligo (https://oligo.readthedocs.io/en/latest/index.html). Oligonucleotide probes are positioned adjacent to the DpnII cut sites on a restriction fragment spanning the IRF8 promoter (chr8:123,259,948-123,260,530) and 70 bp ssDNA biotinylated oligonucleotides were synthetized by Sigma-Aldrich (listed in Resource Table).
To enrich for fragments containing ligation events with IRF8 promoter viewpoint, NuTi Capture-C was performed as previously described (Downes et al., 2021; Downes et al., 2022). Briefly, the 3C libraries prepared from MPP, CDP, cDC1, cDC2 and pDC were sonicated using Covaris S220 to an average size of ∼200 bp using standard settings recommended by the manufacturer (time: 180 s, duty cycle: 10%, peak incident power: 175 W, cycles per burst: 200, temperature: 5-9°C). End repair was performed with the NEBNext Ultra II kit (New England Biolabs, E7645S) using 2 µg of sonicated 3C library in duplicate for each sample. Illumina NEBNext Indices (New England Biolabs, E7500S, and E7335S) were added with a total of 6 cycles of amplification to allow for multiplexing. After this step, duplicates were pooled to increase sample complexity. We enriched samples as per NuTi Capture-C protocol, with two capture rounds in a multiplexed reaction, using 2 µg of each indexed sample as an input for the first capture. The hybridization with biotinylated probes was performed with the KAPA Hyper Capture Reagent Kit (Roche, 9075828001). Each ssDNA biotinylated probe was used at a concentration of 2.9 nM, with a final pool concentration of 5.8 nM, and 4.5 µl of the pooled oligonucleotides were used per sample. Captured DNA was pulled-down with M-270 Streptavidin Dynabeads (Invitrogen, 65305), washed and amplified off the beads with a total of PCR 14 cycles. The DNA obtained after the first capture was used as an input in the second capture round. The experiments were performed for the first and the second biological replicate separately, and then sequenced with NextSeq 550 Illumina System with 300 paired-end or 150 paired-end, respectively.
NuTi Capture-C data analysis
The Capture-C data was analyzed with CapCruncher (v0.1.1a1) pipeline (https://github.com/sims-lab/CapCruncher) in capture mode (Downes et al., 2022). The reads were aligned to the mm9 genome assembly with Bowtie2 (Langmead and Salzberg, 2012), with specific options: -p6--very-sensitive. Viewpoint coordinates used were: chr8:123,259,948-123,260,530, 1000 bp around viewpoint was excluded. The data were normalized to ∼300 kb region around the viewpoint (chr8:123,132,865-123,433,117).
The Capture-C profiles in Figure 1 and Figure S1 show the mean number of unique interactions in two biological replicates, normalized to ∼300 kb region around the viewpoint. Differential tracks were created by subtraction of the mean normalized tracks.
ATAC-seq, ChIP-seq and RNA-seq
ATAC-seq analysis of MPP, CDP, cDC1, cDC2, and pDC was performed by Omni-ATAC-seq (Corces et al., 2017) with minor modifications as described in (Li et al., 2019). RNA-seq analysis and ChIP-seq analysis was done as previously described (Allhoff et al., 2016; Lin et al., 2015).
Plasmids
psPAX2 (Addgene #12260) and pMD2.G (Addgene #12259) for lentiviral packaging and envelope expressing plasmids were kind gifts from Didier Trono, EPFL, Lausanne, Switzerland. The gRNA expressing vector pLKO5.sgRNA.EFS.tRFP (Addgene #57823) and pLKO5.sgRNA.EFS.tRFP657 (Addgene #57824) were kind gifts from Benjamin Ebert, Harvard Medical School, Boston, USA (Heckl et al., 2014).
For lncIRF8 overexpression and rescue, lncIRF8 cDNA was introduced into polyA containing lentivirus vector pGFP-pA to generate plncIRF8-pA. pGFP-pA was constructed from pCIG3 (Addgene #78264) (Caviness et al., 2014) by Gibson Assembly (New England Biolabs, E5510S) (Gibson et al., 2009). In brief, the WPRE element was removed and a polyA signal “AATAAA” was inserted at the 3’ end of GFP to construct pGFP-pA. lncIRF8 cDNA was sub-cloned into pGFP-pA using XhoI and SalI with the primers shown in Resource Table to obtain plncIRF8-pA. CRISPR activation and repression of lncIRF8 and IRF8 promoters were achieved by dCAS9-VP64_GFP (Addgene #61422) (Konermann et al., 2015) and pTet-KRAB-dCas9-GFP (Xu et al., 2021), respectively.
Lentivirus infection
gRNAs, lncIRF8, dCas9-VP64-GFP, and KRAB-dCas9-GFP were delivered into HoxB8 MPP by lentiviral infection. Briefly, lentiviral particles were produced by calcium phosphate transfection (Graham and van der Eb, 1973) of HEK293T cells with psPAX2, pMD2.G, and the lentiviral transfer vector. At 48 and 72 hours after HEK293T cell transfection, supernatant containing virus particles was collected and concentrated using chondroitin sulfate sodium salt (CSS) and polybrene precipitation (Landázuri et al., 2007). HoxB8 MPP were infected twice with concentrated virus and subjected to Ficoll (Pancoll) purification to remove precipitate and dead cells.
Genetically modified HoxB8 MPP cell lines
lncIRF8-promoter KO
Mx-Cas9-GFP HoxB8 MPP were used to generate lncIRF8 promoter knockout (KO) HoxB8 MPP by CRISPR/Cas9. Briefly, two gRNAs for lncIRF8-promoter KO (Resource Table) were designed with the IDT online gRNA design tool (https://eu.idtdna.com/site/order/designtool/index/CRISPR_SEQUENCE). gRNAs were cloned into pLKO5.sgRNA.EFS.tRFP and pLKO5.sgRNA.EFS.tRFP657 vectors (Heckl et al., 2014) using BsmBI-v2, respectively.
One 10 cm dish (Bio-One) with 1.8 million HEK293T cells (70%-80% confluency) in 10 ml DMEM plus supplements (see above) was used to produce gRNA expressing lentivirus particles. HEK293T cells were transfected with 10 μg gRNA vector, 7.5 μg psPAX2, and 2.5 μg pMD2.G per gRNA by calcium phosphate transfection and lentivirus particles were harvested 48 and 72 hours after transfection.
The gRNA expressing lentiviral particles were used to infect 3 million Mx-Cas9-GFP HoxB8 MPP. Cas9 and GFP expression were induced by mIFNα (1000 IU/ml) for 4 hours, followed by FACS sorting for cells expressing the two gRNAs and Cas9 (GFP+ RFP+ RFP657+ cells). Three thousand sorted HoxB8 MPP were then subjected to limiting dilution to obtain single-cell clones.
Single-cell colonies were genotyped by genomic PCR with primers listed in Resource Table. PCR products were sequenced by Eurofins Genomics and sequences were analyzed by SnapGene. Potential off-targets were routinely predicted by online software tools such as CRISPR-Cas9 gRNA checker (https://eu.idtdna.com/site/order/designtool/in-dex/CRISPR_SEQUENCE). Finally, 5 out of 71 single-cell colonies with homozygous deletions were subjected to off-target analysis. The top 2-5 predicted coding or non-coding targets were selected and HoxB8 MPP clones without off-target effects, or where off-target effects occurred in genes that were not expressed in MPP, CDP and DC subsets, were used for further studies (Table S1).
lncIRF8 overexpression and lncIRF8 knockout rescue
lncIRF8 overexpression was performed in wild-type HoxB8 MPP. Lentiviral particles expressing lncIRF8 were produced from ten 6 cm dishes (Bio-One), each consisting of 0.75 million HEK293T cells (70-80% confluency) in 5 ml DMEM with supplements (see above). HEK293T cells were transfected with 5 μg plncIRF8-pA or pGFP-pA, 2.5 μg psPAX2, and 2.5 μg pMD2.G. Lentivirus particles were concentrated as above and used to infect 0.5 million HoxB8 MPP; single-cell clones were generated by limiting dilution and genotyped using the primers listed in Resource Table. Two out of 47 HoxB8 MPP colonies with plncIRF8-pA and 3 out of 19 HoxB8 MPP colonies with pGFP-pA (control) were expanded and subjected to Flt3L-directed DC differentiation.
lncIRF8 knockout rescue was carried out in lncIRF8-promoter KO HoxB8 MPP. FACS sorted cells (100 cells) that genotyped as lncIRF8-promoter KO homozygous deletion cells, were infected with lentiviral particles expressing lncIRF8. Lentiviral infection conditions were the same as for lncIRF8 overexpression in wild-type HoxB8 MPP (see above).
CRISPR activation and CRISPR interference
CRISPR activation and CRISPR interference were performed by infecting wild-type HoxB8 MPP with lentiviral particles expressing dCAS9-VP64_GFP and pTet-KRAB-dCas9-GFP, respectively. The virus particles were produced as in the lncIRF8 overexpression experiments. In brief, virus particles from ten 6 cm dishes were used to infect 0.5 million wild-type HoxB8 MPP, followed by FACS sorting for GFP+ cells expressing dCas9-VP64 or dCas9-KRAB. Doxycycline (1 μg/ml) was used to induce dCas9-KRAB expression 2 days before cell sorting.
gRNAs targeting lncIRF8 and IRF8 promoters were cloned into pLKO5.sgRNA.EFS.tRFP as above. The dCas9-VP64-GFP and dCas9-KRAB-GFP HoxB8 MPP were then infected with specific gRNAs for gene activation and repression. The conditions for gRNA infection were the same as in lncIRF8-promoter KO experiments. Doxycycline (1 μg/ml) was given to the sorted dCas9-KRAB-GFP cells every 3 days to ensure sustained dCas9-KRAB expression.
Flow cytometry analysis and cell sorting
DC subsets were analyzed by flow cytometry using FACS Canto II or LSR Fortessa (both BD Biosciences). The information for flow cytometry antibodies is shown in Resource Table. For live/dead staining, cells were incubated with 3 μl 7-AAD per test for 5-10 min before flow cytometry measurement. Cells were sorted by FACS Aria IIu or FACS Melody, and flow cytometry data were analyzed by FlowJo V10 (all from BD Biosciences). Data on DC frequencies were subjected to the hierarchical clustering and represented in heatmap format using the online tool MORPHEUS (https://software.broadinstitute.org/morpheus/).
Cell transplantation
CD45.1 recipient mice were sublethal irradiated (6.0 Gy, CP-160 Faxitron) 1 day before transplantation. lncIRF8-promoter KO and control HoxB8 MPP (single-cell clones) were expanded in vitro as described above. Cells were injected into recipient mice via the tail vein (5 million cells in 100 μl PBS per mouse). Donor cells from bone marrow and spleen were subjected to flow cytometry analysis at 7 and 14 days after cell transplantation.
RT-qPCR
RNA was isolated by using the NucleoSpin RNA kit (Macherey-Nagel, 740955.250) according to the manufacturer’s instructions. RNA was subjected to cDNA synthesis using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems, 4368814) with Murine RNase Inhibitor (New England Biolabs, M0314S). RT-qPCR was performed by a StepOnePlus™ Real-Time PCR system (Applied Biosystems) with SYBR-green fluorescence (Applied Biosystems, 4385610). The primers for qPCR were listed in Resource Table. Mouse GAPDH was used for normalization of lncIRF8 and IRF8 gene expression.
Identification of lncIRF8
De-novo transcript assembly of RNA-seq data was used to search for unknown transcripts with no coding potential and this identified the pDC specific lncRNA TCONS_00190250 (referred to as lncIRF8) and the cDC1 specific lncRNA TCONS_00190258. In brief, paired end 2×100 bps reads from RNA-seq of MPP, CDP, cDC1, cDC2 and pDC were aligned to mm9 genome using Star aligner (version 2.4) (Dobin et al., 2013) and run for Cufflinks (version 2.0) (Trapnell et al., 2012). Data were subjected to lenient filtering with the parameters: min isoform fraction 0.1% and pre-RNA-fraction of 0.1%, and ribosomal genes were also filtered. Next, all the predicted transcripts were merged with cuffmerge and all transcripts with no overlap with known transcripts in mouse GENCODE were selected for further analysis (Frankish et al., 2019). The coding potential and conservation of coding elements of the lncRNAs were checked with CPAT (Wang et al., 2013) and PhyloCSF (Lin et al., 2011), respectively. lncIRF8 (TCONS_00190250) and TCONS_00190258 show low scores in both analyses, which faithfully supports their role as non-coding genes and exhibit low cross-species conservation.
To further characterize the major transcripts of lncIRF8, 3’ and 5’ end Rapid Amplification of cDNA Ends (RACE) PCR was performed using template-switching RT enzyme mix (New England Biolabs, M0466) and TA cloning kit (Thermo Fisher Scientific, K202020). The primers (listed in Resource Table) used for RACE PCR were synthesized by Eurofins Genomics except for 5’ RACE-TSO, which was from IDT.
3’ RACE PCR
Reverse transcript (RT) and template-switching: 4 μl (10 ng to 1 μg) total RNA (from DC differentiation day 5) were incubated at 80°C for 3 minutes and cooled rapidly on ice. RNA was then incubated with template-switching RT buffer, 1 mM dNTP, 5 mM DTT, 10 μM QT primer (Scotto-Lavino et al., 2006) and 1 μl RT enzyme in 10 μl at room temperature for 5 minutes, followed by 1 hour at 42°C, 10 minutes at 50°C, and 85°C for 5 minutes to inactive the RT enzyme mix and sample was then kept at 4°C and diluted with 20 μl MilliQ water.
First-round PCR: 1 μl of diluted sample was subjected to the first round PCR with Q0 primer and 3’ RACE-GSP-lncIRF8-F1 (10 μM) using Q5 high fidelity DNA polymerase. Second-round PCR: the PCR products from the first round PCR (1:20 dilution) was then used as template for the second round of PCR by using Q1 primer (10 μM), 3’ RACE-GSP-lncIRF8-F2 (10 μM). Q0 and Q1 primers and the PCR programs are described in (Scotto-Lavino et al., 2006). Products from the second-round PCR were purified using the PCR clean-up kit (Macherey-Nagel, 740609.50).
A-tailing and TA cloning: a reaction containing 5 μl of PCR clean-up product in Taq buffer, 1 mM MgCl2, 0.4 mM dATP and 1 μl Taq DNA polymerase in 25 μl was prepared and incubated at 70°C for 20 minutes for A-tailing of PCR products. Five μl of the A-tailed products were subjected to TA cloning into pCR2.1 vector according to the manufacturer’s instruction followed by Sanger sequencing.
5’ RACE PCR
In order to identify the TSS of lncIRF8, template RNA from bone marrow cell-derived pDC was used to perform 5’ RACE PCR using template-switching RT enzyme mix (New England Biolabs, M0466) according to the manufacturer’s instructions. Template switching was by 5’ RACE-GSP-lncIRF8-R2 primer (10 μM) and template switching oligo (TSO) (75 μM). Similar to the 3’ RACE PCR, two rounds of PCR were used to improve PCR specificity. In brief, 5’ RACE-GSP-lncIRF8-R2 (10 μM) and TSO-specific primer (10 μM) were used to perform the first-round PCR, 5’ RACE-GSP-lncIRF8-R1 primer (10 μM) and the TSO-specific primer (10 μM) were used to perform the second round PCR, followed by fragments A-tailing, TA cloning, and Sanger sequencing as described above for 3’ RACE PCR.
Identification of transcription factor binding sites
Transcription factor binding sites (TFBS) in the IRF8 +32 kb enhancer were predicted using a motif matching tool based on the MOODS (Korhonen et al., 2009) and position weight matrixes (PWMs) were obtained from the JASPAR database (Fornes et al., 2020). The bit-score cut-off thresholds were determined by applying the dynamic programming approach as described in (Wilczynski et al., 2009) with an FPR of 0.0001. DC TF were considered and are depicted.
Statistical analysis
Statistical analyses were performed using Prism (GraphPad). Unpaired t test and Multiple t-tests were used to compare data from two groups, two-way ANOVA with Tukey’s multiple comparisons test was used to analyze data from more than two groups.
Acknowledgments
We acknowledge the support of the Interdisciplinary Center for Clinical Research Aachen (IZKF Aachen) FACS Core Facility and Genomics Facility. We thank Magdalena Karpinska and Marieke Oudelaar for help with the Capture-C experiments and analysis, Susanne Schmitz and Paul Wanek for assistance, S. Rose-John for hyper-IL-6, Lisa Weixler and Carmen Schalla for help with enzyme purification, and Thomas Hieronymus for valuable discussion and suggestions.
Part of this work was supported in part by funds from German Research Foundation (DFG) to M.Z. and from the Germany Ministry of Science and Technology (BMBF -Fibromap) and the Interdisciplinary Center for Clinical Research Aachen (IZKF Aachen) from the RWTH Medical Faculty to I.C.. H.X. was supported by a fellowship of China Scholarship Council (CSC) (Grant number 202008080170).
M.A.S.T. was funded by CAPES-Alexander von Humboldt postdoctoral fellowship (99999.001703/2014-05) and donation by U. Lehmann.