Fantauzzo Katherine A, Bazzi Hisham, Jahoda Colin A B, Christiano Angela M
Department of Genetics and Development, Columbia University, New York, NY, USA.
Gene Expr Patterns. 2008 Jan;8(2):51-7. doi: 10.1016/j.modgep.2007.10.006. Epub 2007 Oct 25.
Mutations in the gene encoding the zinc finger transcription factor TRPS1 result in tricho-rhino-phalangeal syndrome, characterized by craniofacial and skeletal abnormalities, and sparse scalp hair. In this study, Trps1 was identified by microarray hybridization analysis as having a complex pattern of spatiotemporal regulation in murine skin during morphogenesis. During early skin development, Trps1 expression decreased in the epidermis while simultaneously increasing in the dermis. Trps1 was specifically expressed in the nuclei of mesenchymal cells during hair follicle morphogenesis. An analysis of Trps1 expression during postnatal murine hair follicle cycling revealed that the protein localized to the nuclei of dermal papillae cells during telogen and anagen. Additionally, we found that Trps1 consistently localized to the nuclei of dermal papillae cells and the highly proliferative epithelial cells of mouse, rat and human hair follicles.
编码锌指转录因子TRPS1的基因突变会导致毛发-鼻-指(趾)综合征,其特征为颅面和骨骼异常以及头皮毛发稀疏。在本研究中,通过微阵列杂交分析确定Trps1在小鼠皮肤形态发生过程中具有复杂的时空调控模式。在皮肤早期发育过程中,Trps1在表皮中的表达下降,而在真皮中的表达同时增加。在毛囊形态发生过程中,Trps1在间充质细胞的细胞核中特异性表达。对出生后小鼠毛囊周期中Trps1表达的分析表明,该蛋白在休止期和生长期定位于毛乳头细胞的细胞核。此外,我们发现Trps1始终定位于小鼠、大鼠和人类毛囊的毛乳头细胞以及高度增殖的上皮细胞的细胞核中。