双壳类动物中 L31 超家族 DNA 转座子的结构与进化

IF 1.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Biology Pub Date : 2024-03-07 DOI:10.1134/s0026893324010114
M. V. Puzakov, L. V. Puzakova
{"title":"双壳类动物中 L31 超家族 DNA 转座子的结构与进化","authors":"M. V. Puzakov, L. V. Puzakova","doi":"10.1134/s0026893324010114","DOIUrl":null,"url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>The mobile genetic elements <i>IS630/Tc1/mariner (ITm</i>) are widespread DNA transposons that make a significant contribution to the evolution of eukaryotic genomes. With the start of large-scale application of next-generation sequencing (NGS) technologies and the emergence of many new whole genome sequences of organisms in nucleotide sequence collections, the <i>ITm</i> elements have been identified in most taxa of the eukaryotic tree of life. Although <i>ITm</i> diversity has been studied in detail, new elements are still found, thus expanding the respective DNA transposon group and calling for review of its classification. Bivalve <i>L31</i> elements were for the first time analyzed in detail to describe their structures, diversity, distribution, and phylogenetic position among the <i>ITm</i> elements. The <i>L31</i> transposons were found to form an independent superfamily of an ancient origin within the <i>ITm</i> group. Rather high diversity was observed within the <i>L31</i> clade; i.e., five phylogenetic clusters were identified. In mollusks, the <i>L31</i> transposons have been detected only in the subclass Autobranchia and predominate in diversity and number in the infraclass Pteriomorphia. A protein encoded by open reading frame 2 (ORF2) was shown to be an integral structural component of almost all full-length <i>L31</i> elements. The results provide for a better understanding of the evolution of particular <i>ITm</i> transposons. Further study of the <i>L31</i> transposons in other taxa (cnidarians) and functional investigation of the ORF2 protein product will help to better understand the evolution of DNA transposons, the mechanisms of their horizontal transfer, and their contribution to eukaryotic biodiversity.</p>","PeriodicalId":18734,"journal":{"name":"Molecular Biology","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structure and Evolution of DNA Transposons of the L31 Superfamily in Bivalves\",\"authors\":\"M. V. Puzakov, L. V. Puzakova\",\"doi\":\"10.1134/s0026893324010114\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3 data-test=\\\"abstract-sub-heading\\\">Abstract</h3><p>The mobile genetic elements <i>IS630/Tc1/mariner (ITm</i>) are widespread DNA transposons that make a significant contribution to the evolution of eukaryotic genomes. With the start of large-scale application of next-generation sequencing (NGS) technologies and the emergence of many new whole genome sequences of organisms in nucleotide sequence collections, the <i>ITm</i> elements have been identified in most taxa of the eukaryotic tree of life. Although <i>ITm</i> diversity has been studied in detail, new elements are still found, thus expanding the respective DNA transposon group and calling for review of its classification. Bivalve <i>L31</i> elements were for the first time analyzed in detail to describe their structures, diversity, distribution, and phylogenetic position among the <i>ITm</i> elements. The <i>L31</i> transposons were found to form an independent superfamily of an ancient origin within the <i>ITm</i> group. Rather high diversity was observed within the <i>L31</i> clade; i.e., five phylogenetic clusters were identified. In mollusks, the <i>L31</i> transposons have been detected only in the subclass Autobranchia and predominate in diversity and number in the infraclass Pteriomorphia. A protein encoded by open reading frame 2 (ORF2) was shown to be an integral structural component of almost all full-length <i>L31</i> elements. The results provide for a better understanding of the evolution of particular <i>ITm</i> transposons. Further study of the <i>L31</i> transposons in other taxa (cnidarians) and functional investigation of the ORF2 protein product will help to better understand the evolution of DNA transposons, the mechanisms of their horizontal transfer, and their contribution to eukaryotic biodiversity.</p>\",\"PeriodicalId\":18734,\"journal\":{\"name\":\"Molecular Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-03-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1134/s0026893324010114\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1134/s0026893324010114","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

摘要移动遗传因子IS630/Tc1/mariner(ITm)是一种广泛存在的DNA转座子,对真核生物基因组的进化做出了重要贡献。随着新一代测序(NGS)技术的大规模应用以及核苷酸序列库中许多新的生物全基因组序列的出现,ITm元件已在真核生物生命树的大多数类群中被鉴定出来。尽管对 ITm 的多样性进行了详细研究,但仍有新的元素被发现,从而扩大了 DNA 转座子组的范围,并要求对其分类进行审查。我们首次详细分析了双壳类 L31 元子,以描述它们的结构、多样性、分布以及在 ITm 元子中的系统发育位置。研究发现,L31 转座子在 ITm 群体中形成了一个独立的、起源古老的超家族。在 L31 支系中观察到了相当高的多样性,即发现了五个系统发生群。在软体动物中,L31 转座子只在自鳃亚纲中被发现,在翼手目亚纲中则以多样性和数量居多。研究结果表明,开放阅读框 2(ORF2)编码的蛋白质是几乎所有全长 L31 转座子的结构组成部分。这些结果有助于更好地了解特定 ITm 转座子的进化过程。对其他类群(刺胞动物)中的 L31 转座子的进一步研究和 ORF2 蛋白产物的功能调查将有助于更好地理解 DNA 转座子的进化、其水平转移的机制及其对真核生物多样性的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Structure and Evolution of DNA Transposons of the L31 Superfamily in Bivalves

Abstract

The mobile genetic elements IS630/Tc1/mariner (ITm) are widespread DNA transposons that make a significant contribution to the evolution of eukaryotic genomes. With the start of large-scale application of next-generation sequencing (NGS) technologies and the emergence of many new whole genome sequences of organisms in nucleotide sequence collections, the ITm elements have been identified in most taxa of the eukaryotic tree of life. Although ITm diversity has been studied in detail, new elements are still found, thus expanding the respective DNA transposon group and calling for review of its classification. Bivalve L31 elements were for the first time analyzed in detail to describe their structures, diversity, distribution, and phylogenetic position among the ITm elements. The L31 transposons were found to form an independent superfamily of an ancient origin within the ITm group. Rather high diversity was observed within the L31 clade; i.e., five phylogenetic clusters were identified. In mollusks, the L31 transposons have been detected only in the subclass Autobranchia and predominate in diversity and number in the infraclass Pteriomorphia. A protein encoded by open reading frame 2 (ORF2) was shown to be an integral structural component of almost all full-length L31 elements. The results provide for a better understanding of the evolution of particular ITm transposons. Further study of the L31 transposons in other taxa (cnidarians) and functional investigation of the ORF2 protein product will help to better understand the evolution of DNA transposons, the mechanisms of their horizontal transfer, and their contribution to eukaryotic biodiversity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Molecular Biology
Molecular Biology 生物-生化与分子生物学
CiteScore
1.30
自引率
8.30%
发文量
78
审稿时长
3 months
期刊介绍: Molecular Biology is an international peer reviewed journal that covers a wide scope of problems in molecular, cell and computational biology including genomics, proteomics, bioinformatics, molecular virology and immunology, molecular development biology, molecular evolution and related areals. Molecular Biology publishes reviews, experimental and theoretical works. Every year, the journal publishes special issues devoted to most rapidly developing branches of physical-chemical biology and to the most outstanding scientists.
期刊最新文献
Triosephosphate Isomerase Inhibition by Resveratrol: A New Mechanism of Anti-Glycolysis in Breast Cancer Silencing of the S-Phase Kinase-Associated Protein 2 Gene (SKP2) Inhibits Proliferation and Migration of Hepatocellular Carcinoma Cells New Epigenetic Markers of Age-Dependent Changes in the Cardiovascular System Amino Acid Substitution Patterns in the E6 and E7 Proteins of HPV Type 16: Phylogeography and Evolution Human eRF1 Translation Regulation
×
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