Earliest Photic Zone Niches Probed by Ancestral Microbial Rhodopsins

Author:

Sephus Cathryn D.1,Fer Evrim123,Garcia Amanda K.12ORCID,Adam Zachary R.45,Schwieterman Edward W.56ORCID,Kacar Betul12ORCID

Affiliation:

1. NASA Center for Early Life and Evolution, University of Wisconsin-Madison , Madison, WI, USA

2. Department of Bacteriology, University of Wisconsin-Madison , Madison, WI, USA

3. Microbiology Doctoral Training Program, University of Wisconsin-Madison , Madison, WI, USA

4. Department of Geoscience, University of Wisconsin-Madison , Madison, WI, USA

5. Blue Marble Space Institute of Science , Seattle, WA, USA

6. Department of Earth and Planetary Sciences, University of California , Riverside, CA, USA

Abstract

Abstract For billions of years, life has continuously adapted to dynamic physical conditions near the Earth’s surface. Fossils and other preserved biosignatures in the paleontological record are the most direct evidence for reconstructing the broad historical contours of this adaptive interplay. However, biosignatures dating to Earth’s earliest history are exceedingly rare. Here, we combine phylogenetic inference of primordial rhodopsin proteins with modeled spectral features of the Precambrian Earth environment to reconstruct the paleobiological history of this essential family of photoactive transmembrane proteins. Our results suggest that ancestral microbial rhodopsins likely acted as light-driven proton pumps and were spectrally tuned toward the absorption of green light, which would have enabled their hosts to occupy depths in a water column or biofilm where UV wavelengths were attenuated. Subsequent diversification of rhodopsin functions and peak absorption frequencies was enabled by the expansion of surface ecological niches induced by the accumulation of atmospheric oxygen. Inferred ancestors retain distinct associations between extant functions and peak absorption frequencies. Our findings suggest that novel information encoded by biomolecules can be used as “paleosensors” for conditions of ancient, inhabited niches of host organisms not represented elsewhere in the paleontological record. The coupling of functional diversification and spectral tuning of this taxonomically diverse protein family underscores the utility of rhodopsins as universal testbeds for inferring remotely detectable biosignatures on inhabited planetary bodies.

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Toward a Natural History of Microbial Life;Annual Review of Earth and Planetary Sciences;2024-07-23

2. An Overview of Exoplanet Biosignatures;Reviews in Mineralogy and Geochemistry;2024-07-01

3. Transforming yeast into a facultative photoheterotroph via expression of vacuolar rhodopsin;Current Biology;2024-02

4. Perplexing Cats and Demons: Pointers to the Quantum-Physical Foundations of Life;Relativity of Evolution;2024

5. Mysteries of metallome evolution: Integrating insights from the Earth and life sciences;Reference Module in Earth Systems and Environmental Sciences;2024

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