Synonymous mutations in representative yeast genes are mostly strongly non-neutral

非同义代换 同义替换 遗传学 生物 中性突变 中性分子进化理论 基因 无声突变 突变 无义突变 突变体 突变率 遗传适应性 错义突变 密码子使用偏好性 基因组
作者
Xukang Shen,Siliang Song,Chuan Li,Jianzhi Zhang
出处
期刊:Nature [Springer Nature]
卷期号:606 (7915): 725-731 被引量:243
标识
DOI:10.1038/s41586-022-04823-w
摘要

Synonymous mutations in protein-coding genes do not alter protein sequences and are thus generally presumed to be neutral or nearly neutral1-5. Here, to experimentally verify this presumption, we constructed 8,341 yeast mutants each carrying a synonymous, nonsynonymous or nonsense mutation in one of 21 endogenous genes with diverse functions and expression levels and measured their fitness relative to the wild type in a rich medium. Three-quarters of synonymous mutations resulted in a significant reduction in fitness, and the distribution of fitness effects was overall similar-albeit nonidentical-between synonymous and nonsynonymous mutations. Both synonymous and nonsynonymous mutations frequently disturbed the level of mRNA expression of the mutated gene, and the extent of the disturbance partially predicted the fitness effect. Investigations in additional environments revealed greater across-environment fitness variations for nonsynonymous mutants than for synonymous mutants despite their similar fitness distributions in each environment, suggesting that a smaller proportion of nonsynonymous mutants than synonymous mutants are always non-deleterious in a changing environment to permit fixation, potentially explaining the common observation of substantially lower nonsynonymous than synonymous substitution rates. The strong non-neutrality of most synonymous mutations, if it holds true for other genes and in other organisms, would require re-examination of numerous biological conclusions about mutation, selection, effective population size, divergence time and disease mechanisms that rely on the assumption that synoymous mutations are neutral.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Jasper应助viming采纳,获得10
1秒前
1秒前
快乐友安发布了新的文献求助10
1秒前
1秒前
1秒前
vitamin发布了新的文献求助10
2秒前
XH完成签到,获得积分10
2秒前
英俊的铭应助齐一凡采纳,获得10
4秒前
晶晶完成签到,获得积分10
4秒前
Herrily发布了新的文献求助10
5秒前
冯佳祥完成签到,获得积分10
5秒前
6秒前
大胆砖头完成签到 ,获得积分10
7秒前
7秒前
在逃公主完成签到,获得积分10
7秒前
HDY发布了新的文献求助10
7秒前
7秒前
彭凯发布了新的文献求助10
8秒前
10秒前
10秒前
深情安青应助无可无不可采纳,获得10
11秒前
杨朝进完成签到,获得积分10
12秒前
月倚樱落时完成签到,获得积分10
13秒前
上官若男应助苏宗旭采纳,获得10
14秒前
彭凯完成签到,获得积分10
14秒前
情怀应助dtcao采纳,获得10
14秒前
14秒前
14秒前
14秒前
14秒前
脑洞疼应助科研通管家采纳,获得10
15秒前
15秒前
CL发布了新的文献求助10
15秒前
Cakoibao应助科研通管家采纳,获得20
15秒前
Cakoibao应助科研通管家采纳,获得20
15秒前
小马甲应助科研通管家采纳,获得10
15秒前
15秒前
Hello应助科研通管家采纳,获得10
15秒前
小二郎应助科研通管家采纳,获得10
15秒前
lx84317261完成签到,获得积分10
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 2000
Research for Social Workers 1000
Psychology and Work Today 800
Mastering New Drug Applications: A Step-by-Step Guide (Mastering the FDA Approval Process Book 1) 800
Kinesiophobia : a new view of chronic pain behavior 600
Signals, Systems, and Signal Processing 510
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5895978
求助须知:如何正确求助?哪些是违规求助? 6707590
关于积分的说明 15732670
捐赠科研通 5018484
什么是DOI,文献DOI怎么找? 2702538
邀请新用户注册赠送积分活动 1649248
关于科研通互助平台的介绍 1598505