19开发中的转化控制

B. Thompson, M. Wickens, J. Kimble
{"title":"19开发中的转化控制","authors":"B. Thompson, M. Wickens, J. Kimble","doi":"10.1101/087969767.48.507","DOIUrl":null,"url":null,"abstract":"Development requires the coordinated expression of selected genes at specific times and in specific cells. Such regulated expression controls the establishment of embryonic axes, the existence of stem cells, and the specification of individual cell fates. Translational control has a key role in this regulation. It is particularly important during early embryogenesis and in the germ line, where transcription is typically quiescent; there, control of translation and mRNA stability are the primary ways to regulate patterns of protein synthesis. Yet, translational regulation continues throughout development and in somatic tissues. In this chapter, we view translational control from a developmental perspective. We discuss four major interfaces at which developmental biology meets molecular regulatory mechanisms: molecular switches, gradients, combinatorial control, and networks. These areas were chosen because they bear on fundamental processes of development. We emphasize instances in which sequence-specific regulatory factors control particular mRNAs, and we do not cover the role of general translation factors (e.g., eIF4E and eIF2α) on growth and differentiation (Chapter 4). MECHANISMS OF TRANSLATIONAL CONTROL: A PRIMER Translation is a multistep process and can be divided into three phases: initiation, elongation, and termination. In principle, translational control can be exerted in any of these phases. We focus in this chapter on initiation, which appears to be the most common point of control during development. Translational initiation involves more than 20 proteins, multiple biochemical complexes, and a series of separable steps (Chapter 4). A complex containing eukaryotic initiation factor 4E (eIF4E) (cap-binding protein) and eIF4G is crucial. At...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"36 1","pages":"507-544"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"17","resultStr":"{\"title\":\"19 Translational Control in Development\",\"authors\":\"B. Thompson, M. Wickens, J. Kimble\",\"doi\":\"10.1101/087969767.48.507\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Development requires the coordinated expression of selected genes at specific times and in specific cells. Such regulated expression controls the establishment of embryonic axes, the existence of stem cells, and the specification of individual cell fates. Translational control has a key role in this regulation. It is particularly important during early embryogenesis and in the germ line, where transcription is typically quiescent; there, control of translation and mRNA stability are the primary ways to regulate patterns of protein synthesis. Yet, translational regulation continues throughout development and in somatic tissues. In this chapter, we view translational control from a developmental perspective. We discuss four major interfaces at which developmental biology meets molecular regulatory mechanisms: molecular switches, gradients, combinatorial control, and networks. These areas were chosen because they bear on fundamental processes of development. We emphasize instances in which sequence-specific regulatory factors control particular mRNAs, and we do not cover the role of general translation factors (e.g., eIF4E and eIF2α) on growth and differentiation (Chapter 4). MECHANISMS OF TRANSLATIONAL CONTROL: A PRIMER Translation is a multistep process and can be divided into three phases: initiation, elongation, and termination. In principle, translational control can be exerted in any of these phases. We focus in this chapter on initiation, which appears to be the most common point of control during development. Translational initiation involves more than 20 proteins, multiple biochemical complexes, and a series of separable steps (Chapter 4). A complex containing eukaryotic initiation factor 4E (eIF4E) (cap-binding protein) and eIF4G is crucial. At...\",\"PeriodicalId\":10493,\"journal\":{\"name\":\"Cold Spring Harbor Monograph Archive\",\"volume\":\"36 1\",\"pages\":\"507-544\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cold Spring Harbor Monograph Archive\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/087969767.48.507\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor Monograph Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/087969767.48.507","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 17

摘要

发育需要在特定的时间和特定的细胞中协调表达选定的基因。这种受调控的表达控制着胚胎轴的建立、干细胞的存在和单个细胞命运的规范。翻译控制在这一调控中起着关键作用。它在早期胚胎发生和种系中尤其重要,在那里转录通常是静止的;在那里,控制翻译和mRNA的稳定性是调节蛋白质合成模式的主要途径。然而,翻译调控在整个发育过程和体细胞组织中持续进行。在本章中,我们从发展的角度来看待翻译控制。我们讨论了发育生物学与分子调控机制的四个主要接口:分子开关、梯度、组合控制和网络。选择这些领域是因为它们关系到发展的基本进程。我们强调序列特异性调控因子控制特定mrna的实例,并且我们没有涵盖一般翻译因子(例如,eIF4E和eIF2α)在生长和分化中的作用(第4章)。翻译控制机制:引物翻译是一个多步骤过程,可分为三个阶段:起始,延伸和终止。原则上,可以在这些阶段中的任何阶段施加平移控制。我们在这一章集中讨论起始,这似乎是开发过程中最常见的控制点。翻译起始涉及20多种蛋白质,多种生化复合物和一系列可分离的步骤(第4章)。含有真核起始因子4E(帽结合蛋白)和eIF4G的复合物至关重要。在…
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
19 Translational Control in Development
Development requires the coordinated expression of selected genes at specific times and in specific cells. Such regulated expression controls the establishment of embryonic axes, the existence of stem cells, and the specification of individual cell fates. Translational control has a key role in this regulation. It is particularly important during early embryogenesis and in the germ line, where transcription is typically quiescent; there, control of translation and mRNA stability are the primary ways to regulate patterns of protein synthesis. Yet, translational regulation continues throughout development and in somatic tissues. In this chapter, we view translational control from a developmental perspective. We discuss four major interfaces at which developmental biology meets molecular regulatory mechanisms: molecular switches, gradients, combinatorial control, and networks. These areas were chosen because they bear on fundamental processes of development. We emphasize instances in which sequence-specific regulatory factors control particular mRNAs, and we do not cover the role of general translation factors (e.g., eIF4E and eIF2α) on growth and differentiation (Chapter 4). MECHANISMS OF TRANSLATIONAL CONTROL: A PRIMER Translation is a multistep process and can be divided into three phases: initiation, elongation, and termination. In principle, translational control can be exerted in any of these phases. We focus in this chapter on initiation, which appears to be the most common point of control during development. Translational initiation involves more than 20 proteins, multiple biochemical complexes, and a series of separable steps (Chapter 4). A complex containing eukaryotic initiation factor 4E (eIF4E) (cap-binding protein) and eIF4G is crucial. At...
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Adult Neurogenesis in Teleost Fish 3 Processing of Yeast Cytoplasmic and Mitochondrial Precusor tRNAs 1 Evolutionary Origin of Bone and Cartilage in Vertebrates 3 Patterning and Differentiation of the Vertebrate Spine Preface/Front Matter
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1