The Transcriptional Logic of Mammalian Neuronal Diversity

Sugino, K.; Clark, E.; Schulmann, A.; Shima, Y.; Wang, L.; Hunt, D. L.; Hooks, B. M.; Trankner, D.; Chandrashekar, J.; Picard, S.; Lemire, A.; Spruston, N.; Hantman, A.; Nelson, S. B.

doi:10.1101/208355

bioRxiv · 10.1101/208355

The Transcriptional Logic of Mammalian Neuronal Diversity

Sugino, K.·Clark, E.·Schulmann, A.·Shima, Y.·Wang, L.·Hunt, D. L.·Hooks, B. M.·Trankner, D.·Chandrashekar, J.·Picard, S.·Lemire, A.·Spruston, N.·Hantman, A.·Nelson, S. B.

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Abstract

The mammalian nervous system is constructed of many cell types, but the principles underlying this diversity are poorly understood. To assess brain-wide transcriptional diversity, we sequenced the transcriptomes of the largest collection of genetically and anatomically identified neuronal classes. Using improved expression metrics that distinguish information content from signal-to-noise-ratio, we found that homeobox transcription factors contain the highest information about cell types and have the lowest noise. Genes that contribute the most to neuronal diversity tend to be long and enriched in factors specifically involved in neuronal function. Genome accessibility measurements reveal that long genes have more candidate regulatory elements arrayed in more distinct patterns. These elements frequently overlap interspersed repeats (mobile elements) and the pattern of repeats is predictive of gene expression. New regulatory sites resulting from elongation of neuronal genes by mobile elements may be an evolutionary force enhancing nervous system complexity.

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Sugino, K., Clark, E., Schulmann, A., Shima, Y., Wang, L., Hunt, D. L., Hooks, B. M., Trankner, D., Chandrashekar, J., Picard, S., Lemire, A., Spruston, N., Hantman, A., Nelson, S. B.. 2017-10-24. The Transcriptional Logic of Mammalian Neuronal Diversity. https://doi.org/10.1101/208355

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