ABSTRACT
Neurons possess highly polarized morphology that require intricate molecular organization, partly facilitated by RNA localization. By localizing specific mRNA, neurons can modulate synaptic features through local translation and subsequent modification of protein concentrations in response to stimuli. The resulting activity-dependent modifications are essential for synaptic plasticity, and consequently, fundamental for learning and memory. Consequently, high-resolution characterization of the spatial distribution of dendritic transcripts and the spatial relationship across transcripts is critical for understanding the pathways and mechanisms underlying synaptic plasticity. In this study, we characterize the spatial distribution of six previously uncharacterized genes (Adap2, Colec12, Dtx3L, Kif5c, Nsmf, Pde2a) within the dendrites at a sub-micrometer scale, using single-molecule fluorescence in situ hybridization (smFISH). We found that spatial distributions of dendritically localized mRNA depended on both dendrite morphology and gene identity that cannot be recreated by diffusion alone, suggesting involvement of active mechanisms. Furthermore, our analysis reveals that dendritically localized mRNAs are likely co-transported and organized into clusters at larger spatial scales, indicating a more complex organization of mRNA within dendrites.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Author official email addresses: Jihoon Kim: jihoonk{at}pennmedicine.upenn.edu, Jean G. Rosario: jrosar{at}sas.upenn.edu, Eric Mendoza: em921{at}scarletmail.rutgers.edu, Da Kuang: kuangda{at}seas.upenn.edu
Addition of Figure 1 to clarify workflow;
