Ancient fish lineages illuminate toll-like receptor diversification in early vertebrate evolution.

IF 2.9 4区 医学 Q2 GENETICS & HEREDITY Immunogenetics Pub Date : 2023-10-01 Epub Date: 2023-08-09 DOI:10.1007/s00251-023-01315-7
Kara B Carlson, Cameron Nguyen, Dustin J Wcisel, Jeffrey A Yoder, Alex Dornburg
{"title":"Ancient fish lineages illuminate toll-like receptor diversification in early vertebrate evolution.","authors":"Kara B Carlson,&nbsp;Cameron Nguyen,&nbsp;Dustin J Wcisel,&nbsp;Jeffrey A Yoder,&nbsp;Alex Dornburg","doi":"10.1007/s00251-023-01315-7","DOIUrl":null,"url":null,"abstract":"<p><p>Since its initial discovery over 50 years ago, understanding the evolution of the vertebrate RAG- mediated adaptive immune response has been a major area of research focus for comparative geneticists. However, how the evolutionary novelty of an adaptive immune response impacted the diversity of receptors associated with the innate immune response has received considerably less attention until recently. Here, we investigate the diversification of vertebrate toll-like receptors (TLRs), one of the most ancient and well conserved innate immune receptor families found across the Tree of Life, integrating genomic data that represent all major vertebrate lineages with new transcriptomic data from Polypteriformes, the earliest diverging ray-finned fish lineage. Our analyses reveal TLR sequences that reflect the 6 major TLR subfamilies, TLR1, TLR3, TLR4, TLR5, TLR7, and TLR11, and also currently unnamed, yet phylogenetically distinct TLR clades. We additionally recover evidence for a pulse of gene gain coincident with the rise of the RAG-mediated adaptive immune response in jawed vertebrates, followed by a period of rapid gene loss during the Cretaceous. These gene losses are primarily concentrated in marine teleost fish and synchronous with the mid Cretaceous anoxic event, a period of rapid extinction for marine species. Finally, we reveal a mismatch between phylogenetic placement and gene nomenclature for up to 50% of TLRs found in clades such as ray-finned fishes, cyclostomes, amphibians, and elasmobranchs. Collectively, these results provide an unparalleled perspective of TLR diversity and offer a ready framework for testing gene annotations in non-model species.</p>","PeriodicalId":13446,"journal":{"name":"Immunogenetics","volume":" ","pages":"465-478"},"PeriodicalIF":2.9000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunogenetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00251-023-01315-7","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/8/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Since its initial discovery over 50 years ago, understanding the evolution of the vertebrate RAG- mediated adaptive immune response has been a major area of research focus for comparative geneticists. However, how the evolutionary novelty of an adaptive immune response impacted the diversity of receptors associated with the innate immune response has received considerably less attention until recently. Here, we investigate the diversification of vertebrate toll-like receptors (TLRs), one of the most ancient and well conserved innate immune receptor families found across the Tree of Life, integrating genomic data that represent all major vertebrate lineages with new transcriptomic data from Polypteriformes, the earliest diverging ray-finned fish lineage. Our analyses reveal TLR sequences that reflect the 6 major TLR subfamilies, TLR1, TLR3, TLR4, TLR5, TLR7, and TLR11, and also currently unnamed, yet phylogenetically distinct TLR clades. We additionally recover evidence for a pulse of gene gain coincident with the rise of the RAG-mediated adaptive immune response in jawed vertebrates, followed by a period of rapid gene loss during the Cretaceous. These gene losses are primarily concentrated in marine teleost fish and synchronous with the mid Cretaceous anoxic event, a period of rapid extinction for marine species. Finally, we reveal a mismatch between phylogenetic placement and gene nomenclature for up to 50% of TLRs found in clades such as ray-finned fishes, cyclostomes, amphibians, and elasmobranchs. Collectively, these results provide an unparalleled perspective of TLR diversity and offer a ready framework for testing gene annotations in non-model species.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
古代鱼类谱系阐明了早期脊椎动物进化中toll样受体的多样性。
自50多年前首次发现以来,了解脊椎动物RAG介导的适应性免疫反应的进化一直是比较遗传学家关注的主要领域。然而,适应性免疫反应的进化新颖性如何影响与先天免疫反应相关的受体的多样性,直到最近才受到相当少的关注。在这里,我们研究了脊椎动物toll样受体(TLRs)的多样性,TLRs是生命之树中发现的最古老、最保守的先天免疫受体家族之一,它将代表所有主要脊椎动物谱系的基因组数据与最早分化的射线鳍鱼类谱系——水龙形目的新转录组数据相结合。我们的分析揭示了反映6个主要TLR亚家族的TLR序列,即TLR1、TLR3、TLR4、TLR5、TLR7和TLR11,以及目前未命名但系统发育不同的TLR分支。此外,我们还发现了与RAG介导的有颌脊椎动物适应性免疫反应的上升相一致的基因获得脉冲的证据,随后在白垩纪出现了一段基因快速缺失的时期。这些基因损失主要集中在海洋硬骨鱼身上,与白垩纪中期的缺氧事件同步,这是一个海洋物种快速灭绝的时期。最后,我们揭示了系统发育位置和基因命名法之间的不匹配,在鳐鱼、环口目、两栖动物和蓝鳃类等分支中发现的TLR高达50%。总之,这些结果为TLR多样性提供了无与伦比的视角,并为测试非模式物种的基因注释提供了一个现成的框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Immunogenetics
Immunogenetics 医学-免疫学
CiteScore
6.20
自引率
6.20%
发文量
48
审稿时长
1 months
期刊介绍: Immunogenetics publishes original papers, brief communications, and reviews on research in the following areas: genetics and evolution of the immune system; genetic control of immune response and disease susceptibility; bioinformatics of the immune system; structure of immunologically important molecules; and immunogenetics of reproductive biology, tissue differentiation, and development.
期刊最新文献
The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearing. Bioinformatic analysis predicts the regulatory function of noncoding SNPs associated with Long COVID-19 syndrome. Decoding the genetic landscape of juvenile dermatomyositis: insights from phosphorylation-associated single nucleotide polymorphisms. The characteristic of HLA-A, HLA-B, HLA-C, HLA-DRB1, HLA-DRB3/4/5, HLA-DQA1, HLA-DQB1, HLA-DPA1, and HLA-DPB1 alleles in Zhejiang Han population. The effect of circulating cytokines on the risk of systemic lupus erythematosus: Mendelian randomization and observational study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1