Chd5 调控转录因子 Six3 促进神经元分化

IF 4 2区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY STEM CELLS Pub Date : 2023-03-17 DOI:10.1093/stmcls/sxad002
Padmina Shrestha, Anbalagan Jaganathan, Dhananjay Huilgol, Carlos Ballon, Yon Hwangbo, Alea A Mills
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引用次数: 0

摘要

染色质域螺旋酶 DNA 结合蛋白 5(Chd5)是一种 ATP 依赖性染色质重塑因子,可促进神经元分化。然而,Chd5 在神经发生过程中的作用机制尚不清楚。在这里,我们利用从 Chd5 缺陷小鼠体内获得的细胞在神经元分化早期和晚期的转录谱分析结果表明,Chd5 通过引导逐步的转录变化来调控神经发生。在神经发生的早期阶段,Chd5 会促进朊病毒转录因子 Six3 的表达,从而抑制 Wnt5a,这是一种对神经元成熟至关重要的非经典 Wnt 配体。Chd5 对神经元成熟因子进行转录抑制的这种能力以前从未被人们认识到,它对神经元的品系规范和成熟都至关重要。因此,Chd5促进了神经干细胞的早期转录变化,从而启动了对神经元命运规范至关重要的转录程序。
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Chd5 Regulates the Transcription Factor Six3 to Promote Neuronal Differentiation.

Chromodomain helicase DNA-binding protein 5 (Chd5) is an ATP-dependent chromatin remodeler that promotes neuronal differentiation. However, the mechanism behind the action of Chd5 during neurogenesis is not clearly understood. Here we use transcriptional profiling of cells obtained from Chd5 deficient mice at early and late stages of neuronal differentiation to show that Chd5 regulates neurogenesis by directing stepwise transcriptional changes. During early stages of neurogenesis, Chd5 promotes expression of the proneural transcription factor Six3 to repress Wnt5a, a non-canonical Wnt ligand essential for the maturation of neurons. This previously unappreciated ability of Chd5 to transcriptionally repress neuronal maturation factors is critical for both lineage specification and maturation. Thus, Chd5 facilitates early transcriptional changes in neural stem cells, thereby initiating transcriptional programs essential for neuronal fate specification.

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来源期刊
STEM CELLS
STEM CELLS 医学-生物工程与应用微生物
CiteScore
10.30
自引率
1.90%
发文量
104
审稿时长
3 months
期刊介绍: STEM CELLS, a peer reviewed journal published monthly, provides a forum for prompt publication of original investigative papers and concise reviews. STEM CELLS is read and written by clinical and basic scientists whose expertise encompasses the rapidly expanding fields of stem and progenitor cell biology. STEM CELLS covers: Cancer Stem Cells, Embryonic Stem Cells/Induced Pluripotent Stem (iPS) Cells, Regenerative Medicine, Stem Cell Technology: Epigenetics, Genomics, Proteomics, and Metabonomics, Tissue-Specific Stem Cells, Translational and Clinical Research.
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