Gupta Bhagwati P, Liu Jing, Hwang Byung J, Moghal Nadeem, Sternberg Paul W
Department of Biology, McMaster University, Hamilton, Ontario, Canada.
Genetics. 2006 Nov;174(3):1315-26. doi: 10.1534/genetics.106.063990. Epub 2006 Sep 15.
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.
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。对该通路组成成分的研究揭示了正向和负向调节因子,它们的作用是调节信号转导级联反应的强度和特异性。我们通过筛选lin-3无外阴表型的抑制子进行了遗传筛选,以鉴定该通路的新调节因子。筛选发现了三个位点,包括gap-1的等位基因和一个由sli-3代表的新基因。我们的遗传上位性实验表明,sli-3在核因子lin-1和sur-2的下游或与之平行发挥作用。sli-3与先前鉴定的let-23信号通路的负向调节因子协同相互作用,并导致细胞过度增殖。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。我们提出,sli-3作为外阴诱导的负向调节因子,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表皮生长因子(EGF)信号通路成分相互作用,但在生存能力和排卵过程中不相互作用。因此,sli-3有助于定义EGF信号诱导外阴的特异性。