Nony P, Prudhomme J C, Couble P
Université Claude-Bernard, CNRS, Centre de Génétique Moléculaire et Cellulaire, UMR 106, Villeurbanne, France.
Biol Cell. 1995;84(1-2):43-52. doi: 10.1016/0248-4900(96)81317-7.
The gene encoding the silk protein P25 is specifically transcribed in the posterior silkgland of Bombyx during larval intermoults and is repressed during moults. By performing in vitro DNA-protein interactions, at least five putative regulatory elements were localized in the 5' flanking region of the gene. The most proximal element, close to the TATA box, interacts with SGFB, a silkgland-specific factor which could be involved in the tissue-specific expression of the gene. A more upstream sequence is recognized by an ubiquitous factor, BMFA, which exhibits cyclical modifications in relation to the moulting cycle and could thus be involved in the temporal control of the gene during the development. A construct containing a reporter gene fused to 1450 bp of P25 5' flanking sequences was integrated into the Drosophila genome and shown to be specifically expressed in the larval salivary gland, the organ homologous to the silkgland. Recurrent deletions of this construct showed that the proximal 254 bp contain all the sequences required for this specific expression. Similar foreign constructs introduced in the silkgland in vivo by a particle delivery system were specifically transcribed in the posterior silkgland but remained silent in the middle silkgland as the endogenous genes. This methodology will be used to assay the function of the defined cis-acting elements in the spatial regulation of expression of P25.
编码丝蛋白P25的基因在幼虫蜕皮间期于家蚕后部丝腺中特异性转录,而在蜕皮期间受到抑制。通过进行体外DNA-蛋白质相互作用,至少五个假定的调控元件定位在该基因的5'侧翼区域。最靠近TATA框的近端元件与SGFB相互作用,SGFB是一种丝腺特异性因子,可能参与该基因的组织特异性表达。一个更上游的序列被一种普遍存在的因子BMFA识别,BMFA在蜕皮周期中表现出周期性修饰,因此可能参与发育过程中该基因的时间调控。一个含有与1450 bp的P25 5'侧翼序列融合的报告基因的构建体被整合到家蝇基因组中,并显示在幼虫唾液腺中特异性表达,唾液腺是与丝腺同源的器官。对该构建体进行反复缺失显示,近端254 bp包含这种特异性表达所需的所有序列。通过粒子递送系统在体内导入丝腺的类似外源构建体在后部丝腺中特异性转录,但在中部丝腺中像内源基因一样保持沉默。这种方法将用于分析确定的顺式作用元件在P25表达的空间调控中的功能。