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HuB/C/D nPTB REST4 and miR-124 regulators of neuronal cell identity are also utilized in the lens

机译:晶状体中还使用了HuB / C / DnPTBREST4和miR-124神经元细胞身份调节剂

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摘要

PurposeAn interlocking network of transcription factors, RNA binding proteins, and miRNAs globally regulates gene expression and alternative splicing throughout development, and ensures the coordinated mutually exclusive expression of non-neural and neuronal forms of these factors during neurogenesis. Striking similarities between lens fiber cell and neuron cell morphology led us to determine if these factors are also used in the lens. HuR and polypyrimidine tract binding protein (PTB) have been described as ‘global regulators’ of RNA alternative splicing, stability, and translation in non-neuronal (including ectodermal) tissues examined to date in diverse species, and REST/NRSF (RE-1 Silencing Transcription Factor/Neuron Restrictive Silencing Factor) represses >2,000 neuronal genes in all non-neuronal tissues examined to date, but has not included the lens. During neurogenesis these factors are replaced by what has been considered neuron-specific HuB/C/D, nPTB, and alternatively spliced REST (REST4), which work with miR-124 to activate this battery of genes, comprehensively reprogram neuronal alternative splicing, and maintain their exclusive expression in post-mitotic neurons.
机译:目的转录因子,RNA结合蛋白和miRNA的互锁网络在整个发育过程中全局调节基因表达和替代剪接,并确保在神经发生过程中这些因子的非神经和神经元形式相互协调地互斥表达。晶状体纤维细胞和神经元细胞形态之间惊人的相似性使我们确定这些因素是否也用于晶状体中。 HuR和多嘧啶束结合蛋白(PTB)被描述为迄今为止在各种物种的非神经元(包括外胚层)组织和REST / NRSF(RE-1)中检测到的RNA替代剪接,稳定性和翻译的``全局调节剂''沉默转录因子/神经元限制性沉默因子可抑制迄今检查的所有非神经元组织中的> 2,000个神经元基因,但尚未包括晶状体。在神经发生过程中,这些因素被认为是神经元特异性的HuB / C / D,nPTB和选择性剪接的REST(REST4)所替代,后者与miR-124共同激活这一系列基因,全面重新编程神经元替代剪接,以及在有丝分裂后神经元中维持它们的独家表达。

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