Frequent birth-and-death events throughout perforin-1 evolution.

IF 3.4 Q1 Agricultural and Biological Sciences BMC Evolutionary Biology Pub Date : 2020-10-19 DOI:10.1186/s12862-020-01698-1
Miguel Araujo-Voces, Víctor Quesada
{"title":"Frequent birth-and-death events throughout perforin-1 evolution.","authors":"Miguel Araujo-Voces, Víctor Quesada","doi":"10.1186/s12862-020-01698-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Through its ability to open pores in cell membranes, perforin-1 plays a key role in the immune system. Consistent with this role, the gene encoding perforin shows hallmarks of complex evolutionary events, including amplification and pseudogenization, in multiple species. A large proportion of these events occurred in phyla for which scarce genomic data were available. However, recent large-scale genomics projects have added a wealth of information on those phyla. Using this input, we annotated perforin-1 homologs in more than eighty species including mammals, reptiles, birds, amphibians and fishes.</p><p><strong>Results: </strong>We have annotated more than 400 perforin genes in all groups studied. Most mammalian species only have one perforin locus, which may contain a related pseudogene. However, we found four independent small expansions in unrelated members of this class. We could reconstruct the full-length coding sequences of only a few avian perforin genes, although we found incomplete and truncated forms of these gene in other birds. In the rest of reptilia, perforin-like genes can be found in at least three different loci containing up to twelve copies. Notably, mammals, non-avian reptiles, amphibians, and possibly teleosts share at least one perforin-1 locus as assessed by flanking genes. Finally, fish genomes contain multiple perforin loci with varying copy numbers and diverse exon/intron patterns. We have also found evidence for shorter genes with high similarity to the C2 domain of perforin in several teleosts. A preliminary analysis suggests that these genes arose at least twice during evolution from perforin-1 homologs.</p><p><strong>Conclusions: </strong>The assisted annotation of new genomic assemblies shows complex patterns of birth-and-death events in the evolution of perforin. These events include duplication/pseudogenization in mammals, multiple amplifications and losses in reptiles and fishes and at least one case of partial duplication with a novel start codon in fishes.</p>","PeriodicalId":9111,"journal":{"name":"BMC Evolutionary Biology","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2020-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574235/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Evolutionary Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12862-020-01698-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Through its ability to open pores in cell membranes, perforin-1 plays a key role in the immune system. Consistent with this role, the gene encoding perforin shows hallmarks of complex evolutionary events, including amplification and pseudogenization, in multiple species. A large proportion of these events occurred in phyla for which scarce genomic data were available. However, recent large-scale genomics projects have added a wealth of information on those phyla. Using this input, we annotated perforin-1 homologs in more than eighty species including mammals, reptiles, birds, amphibians and fishes.

Results: We have annotated more than 400 perforin genes in all groups studied. Most mammalian species only have one perforin locus, which may contain a related pseudogene. However, we found four independent small expansions in unrelated members of this class. We could reconstruct the full-length coding sequences of only a few avian perforin genes, although we found incomplete and truncated forms of these gene in other birds. In the rest of reptilia, perforin-like genes can be found in at least three different loci containing up to twelve copies. Notably, mammals, non-avian reptiles, amphibians, and possibly teleosts share at least one perforin-1 locus as assessed by flanking genes. Finally, fish genomes contain multiple perforin loci with varying copy numbers and diverse exon/intron patterns. We have also found evidence for shorter genes with high similarity to the C2 domain of perforin in several teleosts. A preliminary analysis suggests that these genes arose at least twice during evolution from perforin-1 homologs.

Conclusions: The assisted annotation of new genomic assemblies shows complex patterns of birth-and-death events in the evolution of perforin. These events include duplication/pseudogenization in mammals, multiple amplifications and losses in reptiles and fishes and at least one case of partial duplication with a novel start codon in fishes.

Abstract Image

Abstract Image

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
穿孔素-1进化过程中的频繁出生和死亡事件。
背景:穿孔素-1 能够打开细胞膜上的孔,因此在免疫系统中发挥着关键作用。与这一作用相一致,编码穿孔素的基因在多个物种中显示出复杂进化事件的特征,包括扩增和假基因化。其中大部分事件发生在基因组数据稀缺的门类中。然而,最近的大规模基因组学项目为这些门类增添了大量信息。利用这些信息,我们注释了包括哺乳动物、爬行动物、鸟类、两栖动物和鱼类在内的 80 多个物种中的穿孔素-1 同源物:结果:我们在所研究的所有类群中注释了 400 多个穿孔素基因。大多数哺乳动物只有一个穿孔素基因座,其中可能包含一个相关的假基因。然而,我们在该类动物中的不相关成员中发现了四个独立的小扩展基因。尽管我们在其他鸟类中发现了不完整和截短形式的穿孔素基因,但我们只能重建少数鸟类穿孔素基因的全长编码序列。在爬行动物的其他种类中,穿孔素类基因至少存在于三个不同的基因位点上,其中包含多达 12 个拷贝。值得注意的是,根据侧翼基因的评估,哺乳动物、非鸟类爬行动物、两栖动物以及可能的长尾鱼类至少共享一个穿孔素-1基因座。最后,鱼类基因组包含多个穿孔素基因座,其拷贝数和外显子/内含子模式各不相同。我们还在几种远洋鱼类中发现了与穿孔素 C2 结构域高度相似的较短基因。初步分析表明,这些基因在穿孔素-1同源物的进化过程中至少出现过两次:新基因组组装的辅助注释显示了穿孔素进化过程中复杂的生死事件模式。这些事件包括哺乳动物中的重复/假基因化,爬行动物和鱼类中的多次扩增和丢失,以及鱼类中至少一个带有新起始密码子的部分重复。
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
BMC Evolutionary Biology
BMC Evolutionary Biology 生物-进化生物学
CiteScore
5.80
自引率
0.00%
发文量
0
审稿时长
6 months
期刊介绍: BMC Evolutionary Biology is an open access, peer-reviewed journal that considers articles on all aspects of molecular and non-molecular evolution of all organisms, as well as phylogenetics and palaeontology.
期刊最新文献
Correlation between bioluminescent blinks and swimming behavior in the splitfin flashlight fish Anomalops katoptron Home range of three turtle species in Central Yucatan. A comparative study Variation and plasticity in life-history traits and fitness of wild Arabidopsis thaliana populations are not related to their genotypic and ecological diversity Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China Biodiversity and distribution patterns of blooming jellyfish in the Bohai Sea revealed by eDNA metabarcoding
×
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