Shukla Vallari, Dhiman Neena, Nayak Prajna, Dahanukar Neelesh, Deshpande Girish, Ratnaparkhi Girish S
Department of Biology, Indian Institute of Science Education & Research, Pune 4111008, India.
Department of Molecular Biology, Princeton University, Princeton, NJ 08544
G3 (Bethesda). 2018 May 31;8(6):2027-2041. doi: 10.1534/g3.118.200192.
Proper specification of germline stem cells (GSCs) in ovaries depends on niche derived non-autonomous signaling and cell autonomous components of transcriptional machinery. Stonewall (Stwl), a MADF-BESS family protein, is one of the cell intrinsic transcriptional regulators involved in the establishment and/or maintenance of GSC fate in ovaries. Here we report identification and functional characterization of another member of the same protein family, CG3838/ Brickwall (Brwl) with analogous functions. Loss of function alleles of exhibit age dependent progressive degeneration of the developing ovarioles and loss of GSCs. Supporting the conclusion that the structural deterioration of mutant egg chambers is a result of apoptotic cell death, activated caspase levels are considerably elevated in ovaries. Moreover, as in the case of mutants, on several instances, loss of activity results in fusion of egg chambers and misspecification of the oocyte. Importantly, phenotypes can be partially rescued by germline specific over-expression of arguing for overlapping yet distinct functional capabilities of the two proteins. Taken together with our phylogenetic analysis, these data suggest that and likely share a common MADF-BESS ancestor and they are expressed in overlapping spatiotemporal domains to ensure robust development of the female germline.
卵巢中生殖系干细胞(GSCs)的正确特化取决于龛位衍生的非自主信号传导和转录机制的细胞自主成分。斯通沃尔(Stwl)是一种MADF - BESS家族蛋白,是参与卵巢中GSC命运建立和/或维持的细胞内在转录调节因子之一。在这里,我们报告了同一蛋白家族的另一个成员CG3838/砖墙(Brwl)的鉴定及其功能特性,其具有类似的功能。Brwl功能缺失等位基因表现出发育中的卵巢小管随年龄增长的进行性退化以及GSCs的丧失。支持突变卵室结构退化是凋亡细胞死亡结果这一结论的是,Brwl突变卵巢中活化的半胱天冬酶水平显著升高。此外,与Stwl突变体的情况一样,在一些情况下,Brwl活性丧失会导致卵室融合和卵母细胞的错误特化。重要的是,通过Brwl的生殖系特异性过表达可以部分挽救Brwl突变体表型,这表明这两种蛋白具有重叠但不同的功能能力。结合我们的系统发育分析,这些数据表明Brwl和Stwl可能共享一个共同的MADF - BESS祖先,并且它们在重叠的时空域中表达,以确保雌性生殖系的稳健发育。