Symon Aleisha, Harley Vincent
Molecular Genetics and Development Laboratory, Hudson Institute of Medical Research, Melbourne, Australia; Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia.
Molecular Genetics and Development Laboratory, Hudson Institute of Medical Research, Melbourne, Australia; Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia.
Int J Biochem Cell Biol. 2017 Jun;87:18-22. doi: 10.1016/j.biocel.2017.03.005. Epub 2017 Mar 16.
The SOX9 transcription factor controls the differentiation of many cell types among vertebrates. The SOX9 gene locus is large and complex and contains various tissue-specific enhancers. Individual enhancers direct specific expression of SOX9 in chondrocytes, Sertoli cells and cranial neural crest cells. Human SOX9 mutations can lead to either the complete Campomelic Dysplasia syndrome, or isolated clinical features, depending upon whether the mutation occurs in the coding region or in enhancer regions. Chromatin Immunoprecipitation has helped to define SOX9 control of target gene expression at the genome wide level in hair follicle stem cells and in chondrocytes where SOX9 binds at super-enhancers. SOX9 binding proximal to promoters controls basal cell activity whereas cell type specificity is directed from distal enhancers.
SOX9转录因子控制脊椎动物中多种细胞类型的分化。SOX9基因位点庞大且复杂,包含各种组织特异性增强子。单个增强子指导SOX9在软骨细胞、支持细胞和颅神经嵴细胞中的特异性表达。人类SOX9突变可导致完全性坎波梅尔发育异常综合征或孤立的临床特征,这取决于突变发生在编码区还是增强子区域。染色质免疫沉淀有助于在全基因组水平上确定SOX9对毛囊干细胞和软骨细胞中靶基因表达的控制,在这些细胞中SOX9结合在超级增强子上。SOX9在启动子附近的结合控制基础细胞活性,而细胞类型特异性则由远端增强子指导。