Shaping Drosophila eggs: unveiling the roles of Arpc1 and cpb in morphogenesis

IF 3.9 4区 生物学 Q1 GENETICS & HEREDITY
Poulami Chatterjee, Sandipan Mukherjee, Pralay Majumder
{"title":"Shaping Drosophila eggs: unveiling the roles of Arpc1 and cpb in morphogenesis","authors":"Poulami Chatterjee,&nbsp;Sandipan Mukherjee,&nbsp;Pralay Majumder","doi":"10.1007/s10142-024-01396-x","DOIUrl":null,"url":null,"abstract":"<div><p>The <i>Drosophila</i> egg chamber (EC) starts as a spherical tissue at the beginning. With maturation, the outer follicle cells of EC collectively migrate in a direction perpendicular to the anterior-posterior axis, to shape EC from spherical to ellipsoidal. Filamentous actin (F-actin) plays a significant role in shaping individual migratory cells to the overall EC shape, like in every cell migration. The primary focus of this article is to unveil the function of different Actin Binding Proteins (ABPs) in regulating mature <i>Drosophila</i> egg shape. We have screened 66 ABPs, and the genetic screening data revealed that individual knockdown of Arp2/3 complex genes and the “capping protein β” (<i>cpb</i>) gene have severely altered the egg phenotype. <i>Arpc1</i> and <i>cpb</i> RNAi mediated knockdown resulted in the formation of spherical eggs which are devoid of dorsal appendages. Studies also showed the role of <i>Arpc1</i> and <i>cpb</i> on the number of laid eggs and follicle cell morphology. Furthermore, the depletion of <i>Arpc1</i> and <i>cpb</i> resulted in a change in F-actin quantity. Together, the data indicate that <i>Arpc1</i> and <i>cpb</i> regulate <i>Drosophila</i> egg shape, F-actin management, egg-laying characteristics and dorsal appendages formation.</p></div>","PeriodicalId":574,"journal":{"name":"Functional & Integrative Genomics","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Functional & Integrative Genomics","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s10142-024-01396-x","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

The Drosophila egg chamber (EC) starts as a spherical tissue at the beginning. With maturation, the outer follicle cells of EC collectively migrate in a direction perpendicular to the anterior-posterior axis, to shape EC from spherical to ellipsoidal. Filamentous actin (F-actin) plays a significant role in shaping individual migratory cells to the overall EC shape, like in every cell migration. The primary focus of this article is to unveil the function of different Actin Binding Proteins (ABPs) in regulating mature Drosophila egg shape. We have screened 66 ABPs, and the genetic screening data revealed that individual knockdown of Arp2/3 complex genes and the “capping protein β” (cpb) gene have severely altered the egg phenotype. Arpc1 and cpb RNAi mediated knockdown resulted in the formation of spherical eggs which are devoid of dorsal appendages. Studies also showed the role of Arpc1 and cpb on the number of laid eggs and follicle cell morphology. Furthermore, the depletion of Arpc1 and cpb resulted in a change in F-actin quantity. Together, the data indicate that Arpc1 and cpb regulate Drosophila egg shape, F-actin management, egg-laying characteristics and dorsal appendages formation.

Abstract Image

果蝇卵的形成:揭示 Arpc1 和 cpb 在形态发生中的作用。
果蝇卵室(EC)最初是一个球形组织。随着成熟,卵室的外滤泡细胞集体向垂直于前后轴的方向迁移,使卵室从球形变为椭圆形。丝状肌动蛋白(F-actin)在塑造单个迁移细胞的整体形状方面发挥着重要作用,就像在所有细胞迁移过程中一样。本文的主要重点是揭示不同肌动蛋白结合蛋白(ABPs)在调控成熟果蝇卵形状中的功能。我们筛选了66个ABPs,基因筛选数据显示,单个敲除Arp2/3复合体基因和 "封顶蛋白β"(cpb)基因会严重改变卵的表型。Arpc1 和 cpb RNAi 介导的基因敲除会导致形成没有背侧附属物的球形卵。研究还显示了 Arpc1 和 cpb 对产卵数量和卵泡细胞形态的作用。此外,消耗 Arpc1 和 cpb 还会导致 F-肌动蛋白数量的变化。这些数据表明,Arpc1和cpb调控果蝇卵的形状、F-肌动蛋白管理、产卵特性和背侧附肢的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.50
自引率
3.40%
发文量
92
审稿时长
2 months
期刊介绍: Functional & Integrative Genomics is devoted to large-scale studies of genomes and their functions, including systems analyses of biological processes. The journal will provide the research community an integrated platform where researchers can share, review and discuss their findings on important biological questions that will ultimately enable us to answer the fundamental question: How do genomes work?
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信