在发育中的胚胎中,SMPD3表达通过SOXE因子进行空间调节
Michael L Piacentino1, Aria J Fasse2, Alexis Camacho-Avila2
1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Developmental biology
|December 5, 2023
概括
研究人员确定了控制SMPD3表达的关键基因调节元件,这些元件是在神经顶细胞上皮细胞转移到介质酶细胞 (EMT) 过程中控制SMPD3表达. SOX10直接调节神经细胞迁移至关重要的增强剂,影响脂质代谢.
科学领域:
- 发展生物学 发展生物学
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 皮质到介质细胞转换 (EMT) 涉及显著的血变化,对细胞运动至关重要.
- 神经细胞经历EMT,需要精确调节脂质含量以进行发育过程.
研究的目的:
- 在神经细胞EMT期间识别脂质代谢的转录调节者.
- 发现控制神经细胞中SMPD3基因表达的增强剂序列.
主要方法:
- 报告员试图在SMPD3位置内确定功能增强器区域.
- 突变和淘汰实验,以调查转录调节.
- 染色体免疫沉测序 (ChIP-seq) 用于确定直接的转录因子结合.
主要成果:
- 在SMPD3的三个增强器区域中,第一个内部回顾了内源表达模式.
- SOXE家族的转录因子SOX9和SOX10在迁移的神经细胞中调节SMPD3的表达.
- SOX10直接与迁移神经细胞特有的增强剂结合并调节.
结论:
- SOX10是迁移神经细胞中SMPD3表达的直接调节者.
- 这项研究阐明了EMT期间发育基因调节网络和代谢基因之间的相互作用.
- 这些发现提供了关于在发育过程中对膜脂质含量的转录控制的见解.
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