دورية أكاديمية

The atypical RNA-binding protein Taf15 regulates dorsoanterior neural development through diverse mechanisms in Xenopus tropicalis.

التفاصيل البيبلوغرافية
العنوان: The atypical RNA-binding protein Taf15 regulates dorsoanterior neural development through diverse mechanisms in Xenopus tropicalis.
المؤلفون: DeJong CS; Molecular and Cell Biology Department, Genetics, Genomics and Development Division, University of California, Berkeley, CA 94720, USA., Dichmann DS; Molecular and Cell Biology Department, Genetics, Genomics and Development Division, University of California, Berkeley, CA 94720, USA., Exner CRT; Department of Psychiatry, Weill Institute for Neurosciences, Quantitative Biosciences Institute, University of California San Francisco, San Francisco, CA 94143, USA., Xu Y; Department of Psychiatry, Weill Institute for Neurosciences, Quantitative Biosciences Institute, University of California San Francisco, San Francisco, CA 94143, USA., Harland RM; Molecular and Cell Biology Department, Genetics, Genomics and Development Division, University of California, Berkeley, CA 94720, USA.
المصدر: Development (Cambridge, England) [Development] 2021 Aug 01; Vol. 148 (15). Date of Electronic Publication: 2021 Aug 04.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Company Of Biologists Limited Country of Publication: England NLM ID: 8701744 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-9129 (Electronic) Linking ISSN: 09501991 NLM ISO Abbreviation: Development Subsets: MEDLINE
أسماء مطبوعة: Publication: Cambridge Eng : Company Of Biologists Limited
Original Publication: [Cambridge] : Company of Biologists, [c1987-
مواضيع طبية MeSH: Brain/*metabolism , Neurogenesis/*physiology , Neurons/*metabolism , RNA-Binding Proteins/*metabolism , TATA-Binding Protein Associated Factors/*metabolism , Xenopus/*metabolism, Animals ; Brain/physiology ; Cell Differentiation/physiology ; Exons/physiology ; Female ; Male ; Neurons/physiology ; Xenopus/physiology
مستخلص: The FET family of atypical RNA-binding proteins includes Fused in sarcoma (FUS), Ewing's sarcoma (EWS) and the TATA-binding protein-associate factor 15 (TAF15). FET proteins are highly conserved, suggesting specialized requirements for each protein. Fus regulates splicing of transcripts required for mesoderm differentiation and cell adhesion in Xenopus, but the roles of Ews and Taf15 remain unknown. Here, we analyze the roles of maternally deposited and zygotically transcribed Taf15, which is essential for the correct development of dorsoanterior neural tissues. By measuring changes in exon usage and transcript abundance from Taf15-depleted embryos, we found that Taf15 may regulate dorsoanterior neural development through fgfr4 and ventx2.1. Taf15 uses distinct mechanisms to downregulate Fgfr4 expression, namely retention of a single intron within fgfr4 when maternal and zygotic Taf15 is depleted, and reduction in the total fgfr4 transcript when zygotic Taf15 alone is depleted. The two mechanisms of gene regulation (post-transcriptional versus transcriptional) suggest that Taf15-mediated gene regulation is target and co-factor dependent, contingent on the milieu of factors that are present at different stages of development.
Competing Interests: Competing interests The authors declare no competing or financial interests.
(© 2021. Published by The Company of Biologists Ltd.)
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معلومات مُعتمدة: R01 GM042341 United States GM NIGMS NIH HHS; R35 GM127069 United States GM NIGMS NIH HHS; U01 MH115747 United States MH NIMH NIH HHS
فهرسة مساهمة: Keywords: Xenopus; Embryo development; FET proteins; Maternal deposition; RNA-seq; Transcript regulation
المشرفين على المادة: 0 (RNA-Binding Proteins)
0 (TATA-Binding Protein Associated Factors)
تواريخ الأحداث: Date Created: 20210804 Date Completed: 20211012 Latest Revision: 20220805
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC8353262
DOI: 10.1242/dev.191619
PMID: 34345915
قاعدة البيانات: MEDLINE
الوصف
تدمد:1477-9129
DOI:10.1242/dev.191619