tRNA genes rapidly change in evolution to meet novel translational demands

Author:

Yona Avihu H1,Bloom-Ackermann Zohar1,Frumkin Idan1,Hanson-Smith Victor23,Charpak-Amikam Yoav1,Feng Qinghua4,Boeke Jef D5,Dahan Orna1,Pilpel Yitzhak1

Affiliation:

1. Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel

2. Department of Microbiology, University of California, San Francisco, San Francisco, United States

3. Department of Immunology, University of California, San Francisco, San Francisco, United States

4. Department of Pathology, University of Washington, Seattle, United States

5. Department of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, United States

Abstract

Changes in expression patterns may occur when organisms are presented with new environmental challenges, for example following migration or genetic changes. To elucidate the mechanisms by which the translational machinery adapts to such changes, we perturbed the tRNA pool of Saccharomyces cerevisiae by tRNA gene deletion. We then evolved the deletion strain and observed that the genetic adaptation was recurrently based on a strategic mutation that changed the anticodon of other tRNA genes to match that of the deleted one. Strikingly, a systematic search in hundreds of genomes revealed that anticodon mutations occur throughout the tree of life. We further show that the evolution of the tRNA pool also depends on the need to properly couple translation to protein folding. Together, our observations shed light on the evolution of the tRNA pool, demonstrating that mutation in the anticodons of tRNA genes is a common adaptive mechanism when meeting new translational demands.

Funder

European Research Council

Ben-May Charitable Trust

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference75 articles.

1. Synonymous codon usage in Drosophila melanogaster: natural selection and translational accuracy;Akashi;Genetics,1994

2. Concerted evolution of tRNA genes: intergenic conversion among three unlinked serine tRNA genes in S. pombe;Amstutz;Cell,1985

3. Approximate likelihood-ratio test for branches: a fast, accurate, and powerful alternative;Anisimova;Systematic Biology,2006

4. The yeast initiator tRNAMet can act as an elongator tRNA(Met) in vivo;Aström;Journal of Molecular Biology,1993

5. Trm9-catalyzed tRNA modifications link translation to the DNA damage response;Begley;Molecular Cell,2007

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3