Positive Selection and Inactivation in the Vision and Hearing Genes of Cetaceans

Author:

McGowen Michael R12,Tsagkogeorga Georgia1,Williamson Joseph1,Morin Phillip A3,Rossiter and Stephen J1

Affiliation:

1. School of Biological and Chemical Sciences, Queen Mary, University of London, London, United Kingdom

2. Department of Vertebrate Zoology, Smithsonian National Museum of Natural History, Washington, DC

3. Southwest Fisheries Science Center, National Marine Fisheries Service, NOAA, La Jolla, CA

Abstract

Abstract The transition to an aquatic lifestyle in cetaceans (whales and dolphins) resulted in a radical transformation in their sensory systems. Toothed whales acquired specialized high-frequency hearing tied to the evolution of echolocation, whereas baleen whales evolved low-frequency hearing. More generally, all cetaceans show adaptations for hearing and seeing underwater. To determine the extent to which these phenotypic changes have been driven by molecular adaptation, we performed large-scale targeted sequence capture of 179 sensory genes across the Cetacea, incorporating up to 54 cetacean species from all major clades as well as their closest relatives, the hippopotamuses. We screened for positive selection in 167 loci related to vision and hearing and found that the diversification of cetaceans has been accompanied by pervasive molecular adaptations in both sets of genes, including several loci implicated in nonsyndromic hearing loss. Despite these findings, however, we found no direct evidence of positive selection at the base of odontocetes coinciding with the origin of echolocation, as found in studies examining fewer taxa. By using contingency tables incorporating taxon- and gene-based controls, we show that, although numbers of positively selected hearing and nonsyndromic hearing loss genes are disproportionately high in cetaceans, counts of vision genes do not differ significantly from expected values. Alongside these adaptive changes, we find increased evidence of pseudogenization of genes involved in cone-mediated vision in mysticetes and deep-diving odontocetes.

Funder

Royal Society Newton International Fellowship

European Research Council Starting Grant

Publisher

Oxford University Press (OUP)

Subject

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

Reference93 articles.

1. Mutations of the protocadherin gene PCDH15 cause Usher Syndrome Type 1F;Ahmed;Am J Hum Genet,2001

2. Lack of interphotoreceptor retinoid binding protein caused by homozygous mutation of RBP3 is associated with high myopia and retinal dystrophy;Arno;Invest Ophthalmol Vis Sci,2015

3. The Sonar of Dolphins

4. The function of guanylate cyclase 1 and guanylate cyclase 2 in rod and cone photoreceptors;Baehr;J Biol Chem,2007

5. Controlling the false discovery rate: a practical and powerful approach to multiple testing;Benjamini;J R Stat Soc B,1995

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