Genome reduction occurred in early Prochlorococcus with an unusually low effective population size

Author:

Zhang Hao123,Hellweger Ferdi L4,Luo Haiwei1256

Affiliation:

1. Simon F. S. Li Marine Science Laboratory , School of Life Sciences and State Key Laboratory of Agrobiotechnology, , Shatin, 999077 , Hong Kong SAR

2. The Chinese University of Hong Kong , School of Life Sciences and State Key Laboratory of Agrobiotechnology, , Shatin, 999077 , Hong Kong SAR

3. Shenzhen Research Institute, The Chinese University of Hong Kong , Shenzhen, 518000 , China

4. Water Quality Engineering, Technical University of Berlin , Berlin, 10623 , Germany

5. Institute of Environment , Energy and Sustainability, , Shatin, 999077 , Hong Kong SAR

6. The Chinese University of Hong Kong , Energy and Sustainability, , Shatin, 999077 , Hong Kong SAR

Abstract

Abstract In the oligotrophic sunlit ocean, the most abundant free-living planktonic bacterial lineages evolve convergently through genome reduction. The cyanobacterium Prochlorococcus responsible for 10% global oxygen production is a prominent example. The dominant theory known as “genome streamlining” posits that they have extremely large effective population sizes (Ne) such that selection for metabolic efficiency acts to drive genome reduction. Because genome reduction largely took place anciently, this theory builds on the assumption that their ancestors’ Ne was similarly large. Constraining Ne for ancient ancestors is challenging because experimental measurements of extinct organisms are impossible and alternatively reconstructing ancestral Ne with phylogenetic models gives large uncertainties. Here, we develop a new strategy that leverages agent-based modeling to simulate the changes in the genome-wide ratio of radical to conservative nonsynonymous nucleotide substitution rate (dR/dC) in a possible range of Ne in ancestral populations. This proxy shows expected increases with decreases of Ne only when Ne falls to about 10 k − 100 k or lower, magnitudes characteristic of Ne of obligate endosymbiont species where drift drives genome reduction. Our simulations therefore strongly support a scenario where the primary force of Prochlorococcus genome reduction is drift rather than selection.

Funder

Hong Kong Research Grants Council General Research Fund

Marine Conservation Enhancement Fund

Hong Kong Research Grants Council Area of Excellence Scheme

Chinese University of Hong Kong

Guangdong Basic and Applied Basic Research Foundation

China Postdoctoral Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Ecology, Evolution, Behavior and Systematics,Microbiology

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