Maine Eleanor M, Hansen Dave, Springer Deborah, Vought Valarie E
Department of Biology, Syracuse University, Syracuse, New York 13244, USA.
Genetics. 2004 Oct;168(2):817-30. doi: 10.1534/genetics.104.029355.
In the Caenorhabditis elegans germline, proliferation is induced by Notch-type signaling. Entry of germ cells into meiosis is triggered by activity of the GLD-1 and GLD-2 pathways, which function redundantly to promote meiosis and/or inhibit proliferation. Activation of the germline Notch-type receptor, GLP-1, ultimately inhibits the activities of the GLD-1 and GLD-2 pathways. We previously identified several ego (enhancer of glp-1) genes that promote germline proliferation and interact genetically with the GLP-1 signaling pathway. Here, we show that atx-2 is an ego gene. Our data suggest that ATX-2 is not a positive regulator of the GLP-1 signaling pathway and GLP-1 signaling is not the sole positive regulator of ATX-2 activity. Moreover, our data indicate that GLP-1 must have an additional function, which may be to repress activity of a third meiotic entry pathway that would work in parallel with the GLD-1 and GLD-2 pathways. In addition to its role in proliferation, ATX-2 acts downstream of FOG-2 to promote the female germline fate.
在秀丽隐杆线虫生殖系中,Notch型信号传导诱导细胞增殖。生殖细胞进入减数分裂是由GLD-1和GLD-2信号通路的活性触发的,这两条通路在促进减数分裂和/或抑制增殖方面发挥冗余作用。生殖系Notch型受体GLP-1的激活最终抑制GLD-1和GLD-2信号通路的活性。我们之前鉴定了几个促进生殖系增殖并与GLP-1信号通路发生遗传相互作用的ego(glp-1增强子)基因。在此,我们表明atx-2是一个ego基因。我们的数据表明,ATX-2不是GLP-1信号通路的正向调节因子,并且GLP-1信号传导不是ATX-2活性的唯一正向调节因子。此外,我们的数据表明GLP-1必定具有额外的功能,这可能是抑制第三条减数分裂进入信号通路的活性,该信号通路可能与GLD-1和GLD-2信号通路平行发挥作用。除了其在增殖中的作用外,ATX-2在FOG-2下游发挥作用,以促进雌性生殖系命运。