...
首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Genetic Modifier Screens on Hairless Gain-of-Function Phenotypes Reveal Genes Involved in Cell Differentiation, Cell Growth and Apoptosis in Drosophila melanogaster
【24h】

Genetic Modifier Screens on Hairless Gain-of-Function Phenotypes Reveal Genes Involved in Cell Differentiation, Cell Growth and Apoptosis in Drosophila melanogaster

机译:无毛功能获得型表型的遗传修饰剂筛选揭示了果蝇细胞分化,细胞生长和凋亡相关基因。

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Overexpression of Hairless (H) causes a remarkable degree of tissue loss and apoptosis during imaginal development. H functions as antagonist in the Notch-signaling pathway in Drosophila, and the link to growth and apoptosis is poorly understood. To further our insight into H-mediated apoptosis, we performed two large-scale screens for modifiers of a small rough eye phenotype caused by H overexpression. Both loss- and gain-of-function screens revealed known and new genetic interactors representing diverse cellular functions. Many of them did not cause eye phenotypes on their own, emphasizing a specific genetic interaction with H. As expected, we also identified components of different signaling pathways supposed to be involved in the regulation of cell growth and cell death. Accordingly, some of them also acted as modifiers of proapoptotic genes, suggesting a more general involvement in the regulation of apoptosis. Overall, these screens highlight the importance of H and the Notch pathway in mediating cell death in response to developmental and environmental cues and emphasize their role in maintaining developmental cellular homeostasis.
机译:无毛(H)的过度表达会在想象的发育过程中引起显着程度的组织损失和细胞凋亡。 H在果蝇的Notch信号通路中起拮抗剂的作用,与生长和凋亡的联系了解得很少。为了进一步了解H介导的细胞凋亡,我们进行了两次大规模筛选,筛选由H过度表达引起的小粗糙眼表型的修饰子。功能丧失和获得功能的筛选都揭示了代表各种细胞功能的已知和新的遗传相互作用因子。他们中的许多人并没有单独导致眼睛表型,而是强调了与H的特定遗传相互作用。正如预期的那样,我们还鉴定了可能参与细胞生长和细胞死亡调控的不同信号通路的组成部分。因此,它们中的一些还充当促凋亡基因的修饰物,表明更普遍地参与细胞凋亡的调节。总体而言,这些筛选突出显示了H和Notch通路在介导对发育和环境线索的细胞死亡中的重要性,并强调了它们在维持发育细胞稳态中的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号