As above, so below: Whole transcriptome profiling demonstrates strong molecular similarities between avian dorsal and ventral pallial subdivisions
Autor: | Erich D. Jarvis, Gillian Durieux, Gregory Gedman, Olivier Fedrigo, Matthew T. Biegler, Bettina Haase |
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Rok vydání: | 2021 |
Předmět: |
SCR_021063
Male 0301 basic medicine Arcopallium SCR_021061 SCR_021062 SCR_018190 brain evolution Songbirds Transcriptome transcriptomics 03 medical and health sciences SCR_015954 0302 clinical medicine biology.animal RRIDs RNA‐Seq Animals SCR_010943 SCR_012988 SCR_017036 SCR_014583 Zebra finch Gene Research Articles SCR_003302 SCR_000432 biology avian Sequence Analysis RNA Gene Expression Profiling General Neuroscience Neurogenesis Ridge (biology) Brain Gene Expression Regulation Developmental Vertebrate WGNCA SCR_004277 pallium 030104 developmental biology Evolutionary biology SCR_003092 Nidopallium Finches SCR_001905 030217 neurology & neurosurgery Research Article SCR_015687 |
Zdroj: | The Journal of Comparative Neurology |
ISSN: | 1096-9861 0021-9967 |
DOI: | 10.1002/cne.25159 |
Popis: | Over the last two decades, beginning with the Avian Brain Nomenclature Forum in 2000, major revisions have been made to our understanding of the organization and nomenclature of the avian brain. However, there are still unresolved questions on avian pallial organization, particularly whether the cells above the vestigial ventricle represent distinct populations to those below it or similar populations. To test these two hypotheses, we profiled the transcriptomes of the major avian pallial subdivisions dorsal and ventral to the vestigial ventricle boundary using RNA sequencing and a new zebra finch genome assembly containing about 22,000 annotated, complete genes. We found that the transcriptomes of neural populations above and below the ventricle were remarkably similar. Each subdivision in dorsal pallium (Wulst) had a corresponding molecular counterpart in the ventral pallium (dorsal ventricular ridge). In turn, each corresponding subdivision exhibited shared gene co‐expression modules that contained gene sets enriched in functional specializations, such as anatomical structure development, synaptic transmission, signaling, and neurogenesis. These findings are more in line with the continuum hypothesis of avian brain subdivision organization above and below the vestigial ventricle space, with the pallium as a whole consisting of four major cell populations (intercalated pallium, mesopallium, hyper‐nidopallium, and arcopallium) instead of seven (hyperpallium apicale, interstitial hyperpallium apicale, intercalated hyperpallium, hyperpallium densocellare, mesopallium, nidopallium, and arcopallium). We suggest adopting a more streamlined hierarchical naming system that reflects the robust similarities in gene expression, neural connectivity motifs, and function. These findings have important implications for our understanding of overall vertebrate brain evolution. In 2013, our group examined the expression profiles of 50 genes to develop the continuum hypothesis of avian brain organization. It states that the subdivisions of the dorsal pallium develop continuously with those of the ventral pallium, resulting in a “partial mirror image” organization around the vestigial ventricle divide. However, these claims were challenged due to the small number of genes profiled. The present study uses RNA sequencing to profile the whole transcriptome (~20,000 genes) of the principal subdivisions of the avian telencephalon and confirms the remarkable molecularly similarities between the dorsal and ventral pallium. We recommend adopting a hierarchal nomenclature to reflect these robust molecular similarities. |
Databáze: | OpenAIRE |
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