• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
The theory of facilitated variation.易化变异理论
Proc Natl Acad Sci U S A. 2007 May 15;104 Suppl 1(Suppl 1):8582-9. doi: 10.1073/pnas.0701035104. Epub 2007 May 9.
2
Evolvability.可进化性
Proc Natl Acad Sci U S A. 1998 Jul 21;95(15):8420-7. doi: 10.1073/pnas.95.15.8420.
3
Facilitated variation: how evolution learns from past environments to generalize to new environments.适应性变异:进化如何从过去的环境中学习以推广到新环境。
PLoS Comput Biol. 2008 Nov;4(11):e1000206. doi: 10.1371/journal.pcbi.1000206. Epub 2008 Nov 7.
4
Evolutionary consequences of cryptic genetic variation.隐秘遗传变异的进化后果。
Trends Ecol Evol. 2009 Jun;24(6):305-11. doi: 10.1016/j.tree.2009.02.001. Epub 2009 Mar 26.
5
Developmental Bias and Evolution: A Regulatory Network Perspective.发育偏差与进化:调控网络视角
Genetics. 2018 Aug;209(4):949-966. doi: 10.1534/genetics.118.300995.
6
Phenotypic plasticity and robustness: evolutionary stability theory, gene expression dynamics model, and laboratory experiments.表型可塑性和稳健性:进化稳定性理论、基因表达动力学模型和实验室实验。
Adv Exp Med Biol. 2012;751:249-78. doi: 10.1007/978-1-4614-3567-9_12.
7
A history of phenotypic plasticity accelerates adaptation to a new environment.表型可塑性的历史加速了对新环境的适应。
J Evol Biol. 2011 Sep;24(9):1992-2001. doi: 10.1111/j.1420-9101.2011.02333.x. Epub 2011 Jun 8.
8
On the effects of the modularity of gene regulatory networks on phenotypic variability and its association with robustness.关于基因调控网络的模块性对表型可变性的影响及其与鲁棒性的关联。
Biosystems. 2022 Feb;212:104586. doi: 10.1016/j.biosystems.2021.104586. Epub 2021 Dec 28.
9
Evolutionary constraints or opportunities?进化的限制还是机遇?
Biosystems. 2014 Sep;123:9-18. doi: 10.1016/j.biosystems.2014.06.004. Epub 2014 Jul 16.
10
The molecular origins of evolutionary innovations.进化创新的分子起源。
Trends Genet. 2011 Oct;27(10):397-410. doi: 10.1016/j.tig.2011.06.002. Epub 2011 Aug 27.

引用本文的文献

1
Considering Metabolic Context in Enzyme Evolution and Design.酶进化与设计中的代谢背景考量
Biochemistry. 2025 Aug 19;64(16):3495-3507. doi: 10.1021/acs.biochem.5c00165. Epub 2025 Aug 5.
2
A Notch signal required for a morphological novelty in has antecedent functions in genital disc eversion.在[具体内容未给出]中一种形态新奇所需的Notch信号在生殖盘外翻中具有先前的功能。
Sci Adv. 2025 Jul 18;11(29):eadt7825. doi: 10.1126/sciadv.adt7825. Epub 2025 Jul 16.
3
Dissociation of the mTOR protein interaction network following neuronal activation is altered by Shank3 mutation.神经元激活后mTOR蛋白相互作用网络的解离因Shank3突变而改变。
bioRxiv. 2025 May 23:2025.05.20.655155. doi: 10.1101/2025.05.20.655155.
4
A Notch signal required for a morphological novelty in has antecedent functions in genital disc eversion.在[具体生物]中一种形态新奇性所需的Notch信号在生殖盘外翻中具有先前的功能。 (注:原文中“in ”表述不完整,这里是根据完整翻译需求补充后的内容)
bioRxiv. 2025 May 14:2025.05.09.653167. doi: 10.1101/2025.05.09.653167.
5
The Transformation Experiment of Frederick Griffith II: Inclusion of Cellular Heredity for the Creation of Novel Microorganisms.弗雷德里克·格里菲斯二世的转化实验:纳入细胞遗传以创造新型微生物。
Bioengineering (Basel). 2025 May 15;12(5):532. doi: 10.3390/bioengineering12050532.
6
Single-cell genomics of the mouse olfactory cortex reveals contrasts with neocortex and ancestral signatures of cell type evolution.小鼠嗅觉皮层的单细胞基因组学揭示了与新皮层的差异以及细胞类型进化的祖先特征。
Nat Neurosci. 2025 May;28(5):937-948. doi: 10.1038/s41593-025-01924-3. Epub 2025 Apr 8.
7
Developmental bias as a cause and consequence of adaptive radiation and divergence.发育偏向作为适应性辐射和分化的原因及结果。
Front Cell Dev Biol. 2024 Oct 16;12:1453566. doi: 10.3389/fcell.2024.1453566. eCollection 2024.
8
The legacy and evolvability of Pere Alberch's ideas.佩雷·阿尔贝希思想的遗产与可进化性。
Interface Focus. 2024 Oct 25;14(5):20240011. doi: 10.1098/rsfs.2024.0011. eCollection 2024 Oct 11.
9
The logic of monsters: development and morphological diversity in stem-cell-based embryo models.怪物的逻辑:基于干细胞的胚胎模型的发育与形态多样性
Interface Focus. 2024 Oct 25;14(5):20240023. doi: 10.1098/rsfs.2024.0023. eCollection 2024 Oct 11.
10
A modular circuit coordinates the diversification of courtship strategies.模块化电路协调求偶策略的多样化。
Nature. 2024 Nov;635(8037):142-150. doi: 10.1038/s41586-024-08028-1. Epub 2024 Oct 9.

本文引用的文献

1
Evolution in Mendelian Populations.孟德尔群体中的进化。
Genetics. 1931 Mar;16(2):97-159. doi: 10.1093/genetics/16.2.97.
2
Coordinated control of cell adhesion, polarity, and cytoskeleton underlies Hox-induced organogenesis in Drosophila.细胞黏附、极性和细胞骨架的协同控制是果蝇中Hox诱导器官发生的基础。
Curr Biol. 2006 Nov 21;16(22):2206-16. doi: 10.1016/j.cub.2006.09.029.
3
Parallel genetic origins of pelvic reduction in vertebrates.脊椎动物骨盆缩小的平行遗传起源。
Proc Natl Acad Sci U S A. 2006 Sep 12;103(37):13753-8. doi: 10.1073/pnas.0604706103. Epub 2006 Aug 31.
4
The calmodulin pathway and evolution of elongated beak morphology in Darwin's finches.钙调蛋白途径与达尔文雀细长喙形态的演化
Nature. 2006 Aug 3;442(7102):563-7. doi: 10.1038/nature04843.
5
Genetic and developmental basis of cichlid trophic diversity.丽鱼科鱼类食性多样性的遗传与发育基础。
Heredity (Edinb). 2006 Sep;97(3):211-21. doi: 10.1038/sj.hdy.6800864. Epub 2006 Jul 12.
6
Hox control of organ size by regulation of morphogen production and mobility.Hox通过调控形态发生素的产生和移动来控制器官大小。
Science. 2006 Jul 7;313(5783):63-8. doi: 10.1126/science.1128650. Epub 2006 Jun 1.
7
Spemann's organizer and self-regulation in amphibian embryos.施佩曼组织者与两栖类胚胎的自我调节
Nat Rev Mol Cell Biol. 2006 Apr;7(4):296-302. doi: 10.1038/nrm1855.
8
Structural variation in the human genome.人类基因组中的结构变异。
Nat Rev Genet. 2006 Feb;7(2):85-97. doi: 10.1038/nrg1767.
9
The let-7 MicroRNA family members mir-48, mir-84, and mir-241 function together to regulate developmental timing in Caenorhabditis elegans.let-7微小RNA家族成员mir-48、mir-84和mir-241共同发挥作用,调控秀丽隐杆线虫的发育时间。
Dev Cell. 2005 Sep;9(3):403-14. doi: 10.1016/j.devcel.2005.07.009.
10
Uncovering cryptic genetic variation.揭示隐秘的遗传变异。
Nat Rev Genet. 2004 Sep;5(9):681-90. doi: 10.1038/nrg1426.

易化变异理论

The theory of facilitated variation.

作者信息

Gerhart John, Kirschner Marc

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 May 15;104 Suppl 1(Suppl 1):8582-9. doi: 10.1073/pnas.0701035104. Epub 2007 May 9.

DOI:10.1073/pnas.0701035104
PMID:17494755
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1876433/
Abstract

This theory concerns the means by which animals generate phenotypic variation from genetic change. Most anatomical and physiological traits that have evolved since the Cambrian are, we propose, the result of regulatory changes in the usage of various members of a large set of conserved core components that function in development and physiology. Genetic change of the DNA sequences for regulatory elements of DNA, RNAs, and proteins leads to heritable regulatory change, which specifies new combinations of core components, operating in new amounts and states at new times and places in the animal. These new configurations of components comprise new traits. The number and kinds of regulatory changes needed for viable phenotypic variation are determined by the properties of the developmental and physiological processes in which core components serve, in particular by the processes' modularity, robustness, adaptability, capacity to engage in weak regulatory linkage, and exploratory behavior. These properties reduce the number of regulatory changes needed to generate viable selectable phenotypic variation, increase the variety of regulatory targets, reduce the lethality of genetic change, and increase the amount of genetic variation retained by a population. By such reductions and increases, the conserved core processes facilitate the generation of phenotypic variation, which selection thereafter converts to evolutionary and genetic change in the population. Thus, we call it a theory of facilitated phenotypic variation.

摘要

该理论关注动物通过基因变化产生表型变异的方式。我们认为,自寒武纪以来进化出的大多数解剖学和生理学特征,都是一组在发育和生理学中起作用的保守核心成分的不同成员使用方式发生调控变化的结果。DNA、RNA和蛋白质调控元件的DNA序列发生基因变化会导致可遗传的调控变化,从而指定核心成分的新组合,这些核心成分在动物体内新的时间和地点以新的数量和状态发挥作用。这些成分的新配置构成了新的特征。可行的表型变异所需的调控变化的数量和种类,由核心成分所参与的发育和生理过程的特性决定,特别是由这些过程的模块化、稳健性、适应性、参与弱调控联系的能力以及探索性行为决定。这些特性减少了产生可行的可选择表型变异所需的调控变化的数量,增加了调控靶点的多样性,降低了基因变化的致死性,并增加了种群保留的遗传变异量。通过这些减少和增加,保守的核心过程促进了表型变异的产生,随后选择将其转化为种群中的进化和基因变化。因此,我们将其称为促进表型变异理论。