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Two subunits of the Drosophila mediator complex act together to control cell affinity.

机译:果蝇介体复合物的两个亚基共同作用以控制细胞亲和力。

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The organizing centers for Drosophila imaginal disc development are created at straight boundaries between compartments; these are maintained by differences in cell affinity controlled by selector genes and intercellular signals. skuld and kohtalo encode homologs of TRAP240 and TRAP230, the two largest subunits of the Drosophila mediator complex; mutations in either gene cause identical phenotypes. We show here that both genes are required to establish normal cell affinity differences at the anterior-posterior and dorsal-ventral compartment boundaries of the wing disc. Mutant cells cross from the anterior to the posterior compartment, and can distort the dorsal-ventral boundary in either the dorsal or ventral direction. The Skuld and Kohtalo proteins physically interact in vivo and have synergistic effects when overexpressed, consistent with a skuld kohtalo double-mutant phenotype that is indistinguishable from either single mutant. We suggest that these two subunits do not participate in all of the activities of the mediator complex, but form a submodule that is required to regulate specific target genes, including those that control cell affinity.
机译:果蝇假想盘发育的组织中心是在隔室之间的直线边界处建立的。这些通过选择基因和细胞间信号控制的细胞亲和力的差异得以维持。 skuld和kohtalo编码果蝇介体复合物的两个最大亚基TRAP240和TRAP230的同源物;任一基因中的突变导致相同的表型。我们在这里显示,这两个基因都需要在翼片的前后-和背面-腹侧室边界处建立正常的细胞亲和力差异。突变细胞从前室到后室交叉,并且可以沿背侧或腹侧方向扭曲背腹边界。 Skuld和Kohtalo蛋白在体内发生物理相互作用,并在过度表达时具有协同作用,这与任何一个单一突变体都无法区分的skuld kohtalo双突变表型是一致的。我们建议这两个亚基不参与介体复合物的所有活动,而是形成一个调节特定靶基因(包括控制细胞亲和力的靶基因)所需的亚模块。

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