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The gang of four gene regulates growth and patterning of the developing Drosophila eye.

机译:四个基因的帮会调节果蝇眼的生长和模式。

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We report here the identification of a novel complementation group in the fruit fly Drosophila melanogaster named gang of four (gfr). Mutations in gfr disrupt patterns of cell differentiation in the eye and increase eye size through a proliferative mechanism that can be enhanced by a block in apoptosis. gfr mutant cells show several features of deregulated Ras/MAP kinase activity, including reduced expression of the Capicua growth suppressing transcription factor and synthetically lethality with alleles of the Jun N-terminal kinase phosphatase puckered. gfr alleles also upreguate Notch activity in the eye. Thus, gfr alleles appear to elicit growth and patterning phenotypes via effects on multiple signaling pathways. Moreover, the gfr alleles behave as gain-of-function lesions and overexpress the gene, bruno-3 (bru-3), which is located at the genomic region to which gfr lesions map. Genetic reduction of bru-3 suppresses phenotypes caused by gfr alleles, and like gfr alleles, overexpression of bru-3 depresses levels of Cic protein, indicating that overexpression of bru-3 is central to gfr mutant phenotypes.
机译:我们在这里报告在果蝇果蝇中的一个名为四个人的团伙(gfr)的新型互补组的鉴定。 gfr的突变破坏了眼中细胞分化的模式,并通过一种增殖机制增加了眼睛的大小,这种增殖机制可以通过阻止细胞凋亡来增强。 gfr突变细胞显示出Ras / MAP激酶活性失调的几个特征,包括Capicua生长抑制转录因子的表达降低以及与Jun N端激酶磷酸酶等位基因起皱的合成杀伤力。 gfr等位基因还可以提高眼睛的Notch活性。因此,gfr等位基因似乎通过对多种信号通路的影响来引发生长和模式化表型。此外,gfr等位基因表现为功能获得性损伤,并过表达基因bruno-3(bru-3),该基因位于gfr损伤所定位的基因组区域。 bru-3的基因减少抑制了由gfr等位基因引起的表型,并且像gfr等位基因一样,bru-3的过表达降低了Cic蛋白的水平,这表明bru-3的过表达是gfr突变表型的核心。

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