Qian Zhang, Le Li, Qi Zhang, Yang Zhang, Lizhong Yan, Yanfang Wang, Yuejia Wang, Shaowei Zhao
{"title":"控制果蝇雌性生殖细胞过度生长的基因回路","authors":"Qian Zhang, Le Li, Qi Zhang, Yang Zhang, Lizhong Yan, Yanfang Wang, Yuejia Wang, Shaowei Zhao","doi":"10.1016/j.ydbio.2024.07.016","DOIUrl":null,"url":null,"abstract":"<div><p>Germ cells mutant for <em>bam</em> or <em>bgcn</em> are locked in a germline stem cell (GSC)-like state, leading to tumor-like overgrowth in <em>Drosophila</em> ovaries. Our previous studies have demonstrated that germline overgrowth in <em>bam</em> mutants can be suppressed by defects in the miRNA pathway but enhanced by a null mutation in <em>hippo</em>. However, the genetic epistasis between the miRNA and Hippo pathways still remains unknown. Here, we determined that the miRNA pathway acts downstream of the Hippo pathway in regulating this process. Germ cells mutant for <em>bam</em> or <em>bgcn</em> and defective in both pathways divide very slowly, phenocopying those defective only in the miRNA pathway. In addition, we found that Yki, a key oncoprotein in the Hippo pathway, promotes the growth of both wild-type germ cells and <em>bam</em> mutant GSC-like cells. Like wild-type GSCs, <em>bam</em> mutant GSC-like cells predominantly stay in the G2 phase. Remarkably, many of those defective in the miRNA pathway are arrested before entering this phase. Furthermore, our studies identified <em>bantam</em> as a critical miRNA promoting germline overgrowth in <em>bam</em> or <em>bgcn</em> mutants. Taken together, these findings establish a genetic circuitry controlling <em>Drosophila</em> female germline overgrowth.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetic circuitry controlling Drosophila female germline overgrowth\",\"authors\":\"Qian Zhang, Le Li, Qi Zhang, Yang Zhang, Lizhong Yan, Yanfang Wang, Yuejia Wang, Shaowei Zhao\",\"doi\":\"10.1016/j.ydbio.2024.07.016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Germ cells mutant for <em>bam</em> or <em>bgcn</em> are locked in a germline stem cell (GSC)-like state, leading to tumor-like overgrowth in <em>Drosophila</em> ovaries. Our previous studies have demonstrated that germline overgrowth in <em>bam</em> mutants can be suppressed by defects in the miRNA pathway but enhanced by a null mutation in <em>hippo</em>. However, the genetic epistasis between the miRNA and Hippo pathways still remains unknown. Here, we determined that the miRNA pathway acts downstream of the Hippo pathway in regulating this process. Germ cells mutant for <em>bam</em> or <em>bgcn</em> and defective in both pathways divide very slowly, phenocopying those defective only in the miRNA pathway. In addition, we found that Yki, a key oncoprotein in the Hippo pathway, promotes the growth of both wild-type germ cells and <em>bam</em> mutant GSC-like cells. Like wild-type GSCs, <em>bam</em> mutant GSC-like cells predominantly stay in the G2 phase. Remarkably, many of those defective in the miRNA pathway are arrested before entering this phase. Furthermore, our studies identified <em>bantam</em> as a critical miRNA promoting germline overgrowth in <em>bam</em> or <em>bgcn</em> mutants. Taken together, these findings establish a genetic circuitry controlling <em>Drosophila</em> female germline overgrowth.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-07-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0012160624001969\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0012160624001969","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Germ cells mutant for bam or bgcn are locked in a germline stem cell (GSC)-like state, leading to tumor-like overgrowth in Drosophila ovaries. Our previous studies have demonstrated that germline overgrowth in bam mutants can be suppressed by defects in the miRNA pathway but enhanced by a null mutation in hippo. However, the genetic epistasis between the miRNA and Hippo pathways still remains unknown. Here, we determined that the miRNA pathway acts downstream of the Hippo pathway in regulating this process. Germ cells mutant for bam or bgcn and defective in both pathways divide very slowly, phenocopying those defective only in the miRNA pathway. In addition, we found that Yki, a key oncoprotein in the Hippo pathway, promotes the growth of both wild-type germ cells and bam mutant GSC-like cells. Like wild-type GSCs, bam mutant GSC-like cells predominantly stay in the G2 phase. Remarkably, many of those defective in the miRNA pathway are arrested before entering this phase. Furthermore, our studies identified bantam as a critical miRNA promoting germline overgrowth in bam or bgcn mutants. Taken together, these findings establish a genetic circuitry controlling Drosophila female germline overgrowth.