首页> 美国卫生研究院文献>Molecular and Cellular Biology >Insulation of Enhancer-Promoter Communication by a Gypsy Transposon Insert in the Drosophila cut Gene: Cooperation between Suppressor of Hairy-wing and Modifier of mdg4 Proteins
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Insulation of Enhancer-Promoter Communication by a Gypsy Transposon Insert in the Drosophila cut Gene: Cooperation between Suppressor of Hairy-wing and Modifier of mdg4 Proteins

机译:果蝇切割基因中的吉普赛转座子插入增强-启动子通讯的绝缘:毛翼抑制剂和mdg4蛋白修饰剂之间的合作。

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摘要

The Drosophila mod(mdg4) gene products counteract heterochromatin-mediated silencing of the white gene and help activate genes of the bithorax complex. They also regulate the insulator activity of the gypsy transposon when gypsy inserts between an enhancer and promoter. The Su(Hw) protein is required for gypsy-mediated insulation, and the Mod(mdg4)-67.2 protein binds to Su(Hw). The aim of this study was to determine whether Mod(mdg4)-67.2 is a coinsulator that helps Su(Hw) block enhancers or a facilitator of activation that is inhibited by Su(Hw). Here we provide evidence that Mod(mdg4)-67.2 acts as a coinsulator by showing that some loss-of-function mod(mdg4) mutations decrease enhancer blocking by a gypsy insert in the cut gene. We find that the C terminus of Mod(mdg4)-67.2 binds in vitro to a region of Su(Hw) that is required for insulation, while the N terminus mediates self-association. The N terminus of Mod(mdg4)-67.2 also interacts with the Chip protein, which facilitates activation of cut. Mod(mdg4)-67.2 truncated in the C terminus interferes in a dominant-negative fashion with insulation in cut but does not significantly affect heterochromatin-mediated silencing of white. We infer that multiple contacts between Su(Hw) and a Mod(mdg4)-67.2 multimer are required for insulation. We theorize that Mod(mdg4)-67.2 usually aids gene activation but can also act as a coinsulator by helping Su(Hw) trap facilitators of activation, such as the Chip protein.
机译:果蝇mod(mdg4)基因产物抵消了白色基因的异染色质介导的沉默,并有助于激活Bithorax复合物的基因。当吉普赛人插入增强子和启动子之间时,它们还调节吉普赛人转座子的绝缘子活性。 Su(Hw)蛋白是吉普赛人介导的绝缘所必需的,而Mod(mdg4)-67.2蛋白与Su(Hw)结合。这项研究的目的是确定Mod(mdg4)-67.2是协能剂,其帮助Su(Hw)阻止增强剂还是被Su(Hw)抑制的激活促进剂。在这里,我们通过显示某些功能丧失的mod(mdg4)突变通过切割基因中的吉普赛人插入降低了增强子的阻断作用,从而提供了Mod(mdg4)-67.2充当共发物的证据。我们发现,Mod(mdg4)-67.2的C末端在体外与绝缘所需的Su(Hw)区域结合,而N末端介导自缔合。 Mod(mdg4)-67.2的N末端也与Chip蛋白相互作用,从而促进切割的激活。在C末端截短的Mod(mdg4)-67.2以显性-阴性方式干扰切割的绝缘,但不会显着影响异染色质介导的白色沉默。我们推断,需要Su(Hw)和Mod(mdg4)-67.2多聚体之间的多个接触来进行绝缘。我们认为,Mod(mdg4)-67.2通常有助于基因激活,但也可以通过帮助Su(Hw)捕获激活促进剂(例如Chip蛋白)来充当共筹者。

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