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神经前体bHLH因子Xath5和XNeuroD共同转录靶点的鉴定

Identification of shared transcriptional targets for the proneural bHLH factors Xath5 and XNeuroD.

作者信息

Logan Mary A, Steele Michael R, Van Raay Terence J, Vetter Monica L

机构信息

Department of Neurobiology and Anatomy, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.

出版信息

Dev Biol. 2005 Sep 15;285(2):570-83. doi: 10.1016/j.ydbio.2005.06.033.

Abstract

Proneural basic helix-loop-helix (bHLH) transcription factors are critical positive regulators of neuronal differentiation in a variety of species and are required for proper differentiation of various subtypes of neurons. Although bHLH factors demonstrate some unique functions during neural development, they share the ability to regulate neuronal differentiation, potentially by targeting overlapping sets of genes. To assess this, we performed a screen in ectoderm animal cap tissue to identify direct transcriptional targets shared by two Xenopus ato-related bHLH factors, Xath5 and XNeuroD. Candidate target genes identified in this screen include several transcriptional regulators (Xebf2, Xebf3, XETOR and NKL), an RNA binding protein (elrC), a cell cycle component (Xgadd45gamma) and several novel genes. Overexpression of either Xath5 or XNeuroD induced ectopic in vivo expression of these candidate target genes. Conversely, blocking ato-related bHLH activity prevented endogenous nervous system expression of these genes. Therefore, we have identified a set of genes that can be regulated by multiple ato-related bHLH factors and may function as critical effectors of proneural bHLH-mediated differentiation.

摘要

原神经碱性螺旋-环-螺旋(bHLH)转录因子是多种物种中神经元分化的关键正调控因子,也是各类神经元亚型正常分化所必需的。尽管bHLH因子在神经发育过程中表现出一些独特功能,但它们可能通过靶向重叠的基因集来共同调节神经元分化。为了评估这一点,我们在外胚层动物帽组织中进行了一项筛选,以鉴定两种非洲爪蟾ato相关bHLH因子Xath5和XNeuroD共有的直接转录靶点。在此筛选中鉴定出的候选靶基因包括几种转录调节因子(Xebf2、Xebf3、XETOR和NKL)、一种RNA结合蛋白(elrC)、一种细胞周期成分(Xgadd45γ)以及几个新基因。Xath5或XNeuroD的过表达诱导了这些候选靶基因在体内的异位表达。相反,阻断ato相关bHLH活性会阻止这些基因在体内神经系统中的表达。因此,我们鉴定出了一组可由多种ato相关bHLH因子调节的基因,它们可能作为原神经bHLH介导的分化的关键效应因子发挥作用。

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