Yoder B K, Blumberg D D
Department of Biological Sciences, University of Maryland Baltimore County, Baltimore 21228.
Dev Biol. 1994 May;163(1):38-48. doi: 10.1006/dbio.1994.1121.
The cAMP-inducible prespore gene, PL3, encodes a protein which is a novel component of the spore coat. Unlike the well-characterized spore coat proteins (SP60, SP70, and SP96) which are found in the outer layer of the coat, the PL3 gene product is localized to a subregion of the coat beneath the outer proteinaceous layer. Moreover, a substantial portion of the PL3 protein is tightly associated with the spore coat and not released under the conditions that led to the identification of the other coat proteins. The promoter for this novel spore coat gene is described. Unlike the other coat-protein gene promoters, it lacks the extensive CA-type elements. It contains two short CA boxes and five prominent G-rich regions. Sequential deletions from the 5' end of the promoter which remove both CA boxes as well as two of the G-rich regions reduce the level of expression but do not alter the spatial regulation of expression. Despite the sequence differences, the PL3 promoter still confers correct spatial, temporal, and cell type-specific regulation on a reporter gene. Escherichia coli beta-galactosidase enzyme activity expressed under the control of this PL3 promoter first appears in randomly isolated cells at the loose mound stage. Because of the sensitivity of the assay, beta-galactosidase activity is detectable prior to the appearance of the PL3 protein on Western blots and by immunofluorescence. Later the number of cells staining for beta-galactosidase activity and the intensity of staining increases. During tipped mound, slug, and culminant stages, cells expressing beta-galactosidase under the control of the PL3 promoter are localized to prespore regions and are spatially coincident with cells expressing the PL3 protein.
环磷酸腺苷(cAMP)诱导的前孢子基因PL3编码一种蛋白质,它是孢子壁的一种新型成分。与在外层孢子壁中发现的特征明确的孢子壁蛋白(SP60、SP70和SP96)不同,PL3基因产物定位于蛋白质外层下方的孢子壁亚区域。此外,PL3蛋白的很大一部分与孢子壁紧密结合,在导致鉴定其他壁蛋白的条件下不会释放。描述了这个新型孢子壁基因的启动子。与其他壁蛋白基因启动子不同,它缺乏广泛的CA型元件。它包含两个短的CA盒和五个突出的富含G的区域。从启动子的5'端进行连续缺失,去除了两个CA盒以及两个富含G的区域,这会降低表达水平,但不会改变表达的空间调控。尽管存在序列差异,PL3启动子仍然赋予报告基因正确的空间、时间和细胞类型特异性调控。在这个PL3启动子控制下表达的大肠杆菌β-半乳糖苷酶活性首先出现在松散丘阶段随机分离的细胞中。由于检测方法的敏感性,在Western印迹和免疫荧光检测中,在PL3蛋白出现之前就可以检测到β-半乳糖苷酶活性。后来,染色显示β-半乳糖苷酶活性的细胞数量和染色强度增加。在倾斜丘、蛞蝓和最终阶段,在PL3启动子控制下表达β-半乳糖苷酶的细胞定位于前孢子区域,并且在空间上与表达PL3蛋白的细胞重合。