Abstract
BMP signalling acts as an instructive cue in various developmental processes such as tissue patterning, stem cell proliferation, and differentiation. However, it is not fully understood how this signalling pathway generates different cell-specific outputs. Here we have identified PRDM16 as a key co-factor for BMP signalling. PRDM16 contributes to a repressive role of BMP signalling on neural stem cell (NSC) proliferation. We demonstrate that PRDM16 regulates the genomic distribution of BMP pathway transcription factors, the SMAD4/pSMAD complex, preventing the activation of cell proliferation genes. When Prdm16 is lost, the SMAD complex relocates to nearby genomic regions, leading to abnormal upregulation of BMP target genes. This function of PRDM16 is also required for the specification of choroid plexus (ChP) epithelial cells. Through a single-cell resolution fluorescent in situ approach, we have observed that genes co-repressed by SMAD and PRDM16, such as Wnt7b and several cell cycle regulators, become overexpressed in Prdm16 mutant ChP. Our findings elucidate a mechanism through which SMAD4 and pSMAD1/5/8 repress gene expression. Moreover, our study suggests a regulatory circuit composed of BMP and Wnt signaling, along with PRDM16, in controlling stem cell behaviors.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
The text is updated to make better clarity Main Figure 1,2 and 3 are updated with additional results. Supplementary figure 1, 2 and 3 are updated with additional results. Supplementary 8 is a new supplementary figure with additional results. Altogether, this updated version has the same conclusion as the previous one but with better clarity in the text and more evidences in the figures.
