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首页> 外文期刊>Developmental biology >The Caenorhabditis elegans mel-11 Myosin Phosphatase Regulatory Subunit Affects Tissue Contraction in the Somatic Gonad and the Embryonic Epidermis and Genetically Interacts with the Rac Signaling Pathway
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The Caenorhabditis elegans mel-11 Myosin Phosphatase Regulatory Subunit Affects Tissue Contraction in the Somatic Gonad and the Embryonic Epidermis and Genetically Interacts with the Rac Signaling Pathway

机译:秀丽隐杆线虫mel-11肌球蛋白磷酸酶调节亚基影响体细胞性腺和胚表皮的组织收缩,并与Rac信号通路遗传相互作用。

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摘要

Caenorhabditis elegans embryonic elongation is driven by cell shape changes that cause a contraction of the epidermal cell layer enclosing the embryo. We have previously shown that this process requires a Rho-associated kinase (LET-502) and is opposed by the activity of a myosin phosphatase regulatory subunit (MEL-11). We not extend our characterization and show that mel-11 activity is required both in the epidermis during embryonic elongation and in the spermatheca of the adult somatic gonad. let-502 and mel-11 reporter gene constructs show reciprocal expression patterns in the embryonic epidermis and the spermatheca, and mutations of the two genes have opposite effects in these two tissues. These results are consistent with let-502 and mel-11 mediating tissue contraction and relaxation, respectively. We also find that mel-11 embryonic inviability is genetically enhanced by mutations in a Rac signaling pathway, suggesting that Rac potentials or acts in parallel with the activity of the myosin phosphatase complex. Since Rho has been implicated in promoting cellular contraction, our results support a mechanism by which epithelial morphogenesis is regulated by the counteracting activities of Rho and Rac.
机译:秀丽隐杆线虫的胚胎伸长是由细胞形状变化驱动的,该细胞形状变化引起包围胚胎的表皮细胞层的收缩。先前我们已经表明,该过程需要Rho相关激酶(LET-502),并且与肌球蛋白磷酸酶调节亚基(MEL-11)的活性相反。我们没有扩展我们的表征,并表明在胚胎伸长过程中表皮和成年体细胞性腺的精子中都需要mel-11活性。 let-502和mel-11报告基因构建体在胚胎表皮和精囊中表现出相互表达模式,并且两个基因的突变在这两个组织中具有相反的作用。这些结果分别与let-502和mel-11介导组织的收缩和松弛相一致。我们还发现mel-11胚胎的生存能力在基因上通过Rac信号通路中的突变得到增强,这表明Rac电位或与肌球蛋白磷酸酶复合物的活性并行。由于Rho与促进细胞收缩有关,因此我们的研究结果支持了Rho和Rac的抵消活性调节上皮形态发生的机制。

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