Fischer D F, Sark M W, Lehtola M M, Gibbs S, van de Putte P, Backendorf C
Leiden Institute of Chemistry, Leiden University, Leiden, 2300 RA, The Netherlands.
Genomics. 1999 Jan 1;55(1):88-99. doi: 10.1006/geno.1998.5622.
SPRR3, a member of the SPRR family of cornified envelope precursor proteins, is expressed in oral and esophageal epithelia, where it is strictly linked to keratinocyte terminal differentiation. This gene is characterized by intragenic duplications that have created the characteristic proline-rich repeats in the coding sequence, an alternative noncoding exon, and a 200-bp polypyrimidine tract in the promoter region. Mutational analysis of the promoter region and transient transfection in normal human keratinocytes showed that in addition to the polypyrimidine tract, multiple regulatory elements are involved in differentiation-specific expression. These elements include a high-affinity Ets binding site bound by ESE-1, an AP-1 site (TRE) recognized by the Jun/Fos family of transcription factors, and an ATF/CRE bound by Jun/Fos and ATF factors. The repositioning of the SPRR3 Ets binding site during evolution has a major effect on the relative contribution of this site to promoter activity.
丝聚蛋白相关蛋白3(SPRR3)是角质化包膜前体蛋白SPRR家族的成员之一,在口腔和食管上皮中表达,在那里它与角质形成细胞的终末分化密切相关。该基因的特征在于基因内重复,这些重复在编码序列中产生了富含脯氨酸的特征性重复序列、一个可变的非编码外显子以及启动子区域中的一个200 bp的多嘧啶序列。对启动子区域的突变分析以及在正常人角质形成细胞中的瞬时转染表明,除了多嘧啶序列外,多个调控元件参与了分化特异性表达。这些元件包括一个由ESE-1结合的高亲和力Ets结合位点、一个由Jun/Fos转录因子家族识别的AP-1位点(TRE)以及一个由Jun/Fos和ATF因子结合的ATF/CRE。SPRR3 Ets结合位点在进化过程中的重新定位对该位点对启动子活性的相对贡献有重大影响。