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sli-3 Negatively Regulates the LET-23/Epidermal Growth Factor Receptor-Mediated Vulval Induction Pathway in Caenorhabditis elegans

机译:sli-3负调控线虫秀丽隐杆线虫的LET-23 /表皮生长因子受体介导的外阴诱导途径。

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摘要

The LIN-3–LET-23-mediated inductive signaling pathway plays a major role during vulval development in C. elegans. Studies on the components of this pathway have revealed positive as well as negative regulators that function to modulate the strength and specificity of the signal transduction cascade. We have carried out genetic screens to identify new regulators of this pathway by screening for suppressors of lin-3 vulvaless phenotype. The screens recovered three loci including alleles of gap-1 and a new gene represented by sli-3. Our genetic epistasis experiments suggest that sli-3 functions either downstream or in parallel to nuclear factors lin-1 and sur-2. sli-3 synergistically interacts with the previously identified negative regulators of the let-23 signaling pathway and causes excessive cell proliferation. However, in the absence of any other mutation sli-3 mutant animals display wild-type vulval induction and morphology. We propose that sli-3 functions as a negative regulator of vulval induction and defines a branch of the inductive signaling pathway. We provide evidence that sli-3 interacts with the EGF signaling pathway components during vulval induction but not during viability and ovulation processes. Thus, sli-3 helps define specificity of the EGF signaling to induce the vulva.
机译:LIN-3–LET-23介导的诱导信号通路在秀丽隐杆线虫的外阴发育过程中起主要作用。对这种途径的组成部分的研究表明,正负调节剂可调节信号转导级联的强度和特异性。我们已经进行了遗传筛选,以通过筛选lin-3无外阴表型的抑制剂来鉴定该途径的新调节子。筛选回收了三个基因座,包括gap-1等位基因和一个由sli-3代表的新基因。我们的遗传上位实验表明,sli-3在下游或与核因子lin-1和sur-2平行起作用。 sli-3与let-23信号通路的先前鉴定的负调节剂协同作用,并引起过度的细胞增殖。然而,在没有任何其他突变的情况下,sli-3突变动物表现出野生型外阴诱导和形态。我们建议sli-3作为外阴诱导的负调节剂,并定义了诱导信号通路的一个分支。我们提供的证据表明,sli-3在外阴诱导过程中与EGF信号通路成分相互作用,但在生存力和排卵过程中没有相互作用。因此,sli-3有助于定义EGF信号传导的特异性以诱导外阴。

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