首页> 外文期刊>Insect Molecular Biology >Transcription factors BmPOUM2 and Bm beta FTZ-F1 are involved in regulation of the expression of the wing cuticle protein gene BmWCP4 in the silkworm, Bombyx mori
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Transcription factors BmPOUM2 and Bm beta FTZ-F1 are involved in regulation of the expression of the wing cuticle protein gene BmWCP4 in the silkworm, Bombyx mori

机译:转录因子BmPOUM2和Bm beta FTZ-F1参与家蚕Bombyx mori翅角质层蛋白基因BmWCP4的表达调控

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In Bombyx mori, the wing cuticle protein gene BmWCP4 is expressed specifically in the epidermis at the onset and mid-stage of pupation and is responsible for the formation of the pupal cuticle during the larval-pupal metamorphosis. The gene consists of four exons and three introns and is present as a single copy in the genome. Its expression was up-regulated by 20-hydroxyecdysone (20E) and the 20E-induced expression was suppressed by juvenile hormone (JH) III. The upstream regulatory sequence region of the BmWCP4 gene was cloned and the regulatory elements responsible for 20E induction were identified. Two cis-regulatory elements (CREs) bound by the transcription factors BmPOUM2 and Bm beta FTZ-F1 were identified that mediated 20E-regulated expression of this gene. An electrophoretic mobility shift assay detected two nuclear proteins isolated from the epidermis and the BmN cell line that specifically bound to the POU and beta FTZ-F1 CREs, respectively. BmPOUM2 recombinant protein explicitly bound to the POU CRE. Developmental and 20E-induced expression of the BmWCP4, BmPOUM2 and Bm beta FTZ-F1 genes showed that BmPOUM2 and Bm beta FTZ-F1 were initially expressed, followed by BmWCP4. These data suggest that the 20E-induced expression of BmWCP4 is mediated by the transcription factors BmPOUM2 and Bm beta FTZ-F1 binding to their CREs in the regulatory sequence region of the BmWCP4 gene.
机译:在家蚕中,翅角质层蛋白基因BmWCP4在化up的开始和中期阶段在表皮中特异性表达,并在幼虫-pu变态过程中负责形成cut角质层。该基因由四个外显子和三个内含子组成,在基因组中以单拷贝形式存在。它的表达被20-羟基蜕皮激素(20E)上调,而20E诱导的表达被少年激素(JH)III抑制。克隆了BmWCP4基因的上游调控序列区域,并鉴定了负责20E诱导的调控元件。转录因子BmPOUM2和Bm beta FTZ-F1绑定的两个顺式调节元件(CREs)被确定介导20E调节该基因的表达。电泳迁移率迁移分析检测到从表皮和BmN细胞系中分离出的两种核蛋白,分别与POU和βFTZ-F1 CRE特异性结合。 BmPOUM2重组蛋白与POU CRE明确结合。 BmWCP4,BmPOUM2和BmβFTZ-F1基因的发育和20E诱导表达表明BmPOUM2和BmβFTZ-F1最初表达,然后是BmWCP4。这些数据表明,BmWCP4的20E诱导表达是由转录因子BmPOUM2和BmβFTZ-F1结合到BmWCP4基因的调控序列区域中的CRE介导的。

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