应用定向 Y 染色体捕获富集技术提高美国原住民单倍群 Q 的分辨率

IF 3.3 2区 医学 Q2 GENETICS & HEREDITY
Zehra Köksal, Claus Børsting, Graciela Bailliet, Germán Burgos, Elizeu Carvalho, Andrea Casas-Vargas, Adriana Castillo, Marilia Brito Gomes, Beatriz Martínez, Humberto Ossa, María Laura Parolin, Alfredo Quiroz, Ulises Toscanini, William Usaquén, Irina F. Velázquez, Carlos Vullo, Leonor Gusmão, Vania Pereira
{"title":"应用定向 Y 染色体捕获富集技术提高美国原住民单倍群 Q 的分辨率","authors":"Zehra Köksal,&nbsp;Claus Børsting,&nbsp;Graciela Bailliet,&nbsp;Germán Burgos,&nbsp;Elizeu Carvalho,&nbsp;Andrea Casas-Vargas,&nbsp;Adriana Castillo,&nbsp;Marilia Brito Gomes,&nbsp;Beatriz Martínez,&nbsp;Humberto Ossa,&nbsp;María Laura Parolin,&nbsp;Alfredo Quiroz,&nbsp;Ulises Toscanini,&nbsp;William Usaquén,&nbsp;Irina F. Velázquez,&nbsp;Carlos Vullo,&nbsp;Leonor Gusmão,&nbsp;Vania Pereira","doi":"10.1155/2024/3046495","DOIUrl":null,"url":null,"abstract":"<p>Y-chromosomal haplogroups and the Y-SNPs defining them are relevant for the exploration of male lineages, inference of paternal ancestry, and reconstruction of migration pathways, to name a few. Currently, over 300,000 Y-SNPs have been reported, defining 20 main haplogroups. However, ascertainment bias in the investigations has led to some haplogroups being overlooked, which hinders a representative depiction of certain populations and their migration events. For migration pattern analyses of the first settlers of the Americas, the Native American main founding lineage Q-M3 needs to be further investigated to allow clear genetic differentiation of individuals of different ethnogeographic origins. To increase the resolution within this haplogroup, a total of 7.45 Mb of the Y chromosome of 59 admixed South Americans of haplogroup Q was targeted for sequencing using hybridization capture enrichment. Data were combined with 218 publicly available sequences of Central and South Americans of haplogroup Q. After rigorous data processing, variants not meeting the quality criteria were excluded and 4128 reliable Y-SNPs were reported. A total of 2224 Y-SNPs had previously unknown positions in the phylogenetic tree, and 1291 of these are novel. The phylogenetic relationships between the Y-SNPs were established using the software SNPtotree in order to report a redesigned phylogenetic tree containing 300 branches, defined by 3400 Y-SNPs. The new tree introduces 117 previously undescribed branches and is the most comprehensive phylogenetic tree of the Native American haplogroup Q lineages to date. The 214 sequences were assigned to 135 different low- to high-resolution branches, while in the previous phylogenetic tree, only 195 sequences could be sorted into 14 low-resolution branches with the same quality criteria. The improved genetic differentiation of subhaplogroup Q-M3 has a great potential to resolve migration patterns of Native Americans.</p>","PeriodicalId":13061,"journal":{"name":"Human Mutation","volume":"2024 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/2024/3046495","citationCount":"0","resultStr":"{\"title\":\"Application of Targeted Y-Chromosomal Capture Enrichment to Increase the Resolution of Native American Haplogroup Q\",\"authors\":\"Zehra Köksal,&nbsp;Claus Børsting,&nbsp;Graciela Bailliet,&nbsp;Germán Burgos,&nbsp;Elizeu Carvalho,&nbsp;Andrea Casas-Vargas,&nbsp;Adriana Castillo,&nbsp;Marilia Brito Gomes,&nbsp;Beatriz Martínez,&nbsp;Humberto Ossa,&nbsp;María Laura Parolin,&nbsp;Alfredo Quiroz,&nbsp;Ulises Toscanini,&nbsp;William Usaquén,&nbsp;Irina F. Velázquez,&nbsp;Carlos Vullo,&nbsp;Leonor Gusmão,&nbsp;Vania Pereira\",\"doi\":\"10.1155/2024/3046495\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Y-chromosomal haplogroups and the Y-SNPs defining them are relevant for the exploration of male lineages, inference of paternal ancestry, and reconstruction of migration pathways, to name a few. Currently, over 300,000 Y-SNPs have been reported, defining 20 main haplogroups. However, ascertainment bias in the investigations has led to some haplogroups being overlooked, which hinders a representative depiction of certain populations and their migration events. For migration pattern analyses of the first settlers of the Americas, the Native American main founding lineage Q-M3 needs to be further investigated to allow clear genetic differentiation of individuals of different ethnogeographic origins. To increase the resolution within this haplogroup, a total of 7.45 Mb of the Y chromosome of 59 admixed South Americans of haplogroup Q was targeted for sequencing using hybridization capture enrichment. Data were combined with 218 publicly available sequences of Central and South Americans of haplogroup Q. After rigorous data processing, variants not meeting the quality criteria were excluded and 4128 reliable Y-SNPs were reported. A total of 2224 Y-SNPs had previously unknown positions in the phylogenetic tree, and 1291 of these are novel. The phylogenetic relationships between the Y-SNPs were established using the software SNPtotree in order to report a redesigned phylogenetic tree containing 300 branches, defined by 3400 Y-SNPs. The new tree introduces 117 previously undescribed branches and is the most comprehensive phylogenetic tree of the Native American haplogroup Q lineages to date. The 214 sequences were assigned to 135 different low- to high-resolution branches, while in the previous phylogenetic tree, only 195 sequences could be sorted into 14 low-resolution branches with the same quality criteria. The improved genetic differentiation of subhaplogroup Q-M3 has a great potential to resolve migration patterns of Native Americans.</p>\",\"PeriodicalId\":13061,\"journal\":{\"name\":\"Human Mutation\",\"volume\":\"2024 1\",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1155/2024/3046495\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Mutation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1155/2024/3046495\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Mutation","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/2024/3046495","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

Y 染色体单倍群和定义这些单倍群的 Y-SNPs 与探索男性血统、推断父系祖先和重建迁徙路径等相关。目前,已报道的 Y-SNPs 超过 30 万个,定义了 20 个主要单倍群。然而,调查中的确认偏差导致一些单倍群被忽视,从而阻碍了对某些人群及其迁徙事件的代表性描述。为了分析美洲第一批定居者的迁徙模式,需要进一步研究美洲原住民的主要创始系 Q-M3,以便对不同人种起源的个体进行明确的遗传区分。为了提高该单倍群的分辨率,我们利用杂交捕获富集法对 59 个混血南美 Q 单倍群的 Y 染色体进行了总计 7.45 Mb 的测序。经过严格的数据处理,排除了不符合质量标准的变异,报告了 4128 个可靠的 Y-SNPs 。共有 2224 个 Y-SNPs 在系统发生树中的位置以前未知,其中 1291 个是新的。利用 SNPtotree 软件确定了 Y-SNPs 之间的系统发生关系,从而报告了一棵重新设计的系统发生树,该树包含 300 个分支,由 3400 个 Y-SNPs 定义。新的系统发生树引入了 117 个以前没有描述过的分支,是迄今为止最全面的美洲原住民 Q 单倍群系统发生树。214 个序列被分配到 135 个不同的低分辨率到高分辨率分支中,而在以前的系统发生树中,在相同质量标准下,只有 195 个序列能被分类到 14 个低分辨率分支中。Q-M3 亚单系的遗传分化得到改善,这对研究美洲原住民的迁移模式具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Application of Targeted Y-Chromosomal Capture Enrichment to Increase the Resolution of Native American Haplogroup Q

Application of Targeted Y-Chromosomal Capture Enrichment to Increase the Resolution of Native American Haplogroup Q

Y-chromosomal haplogroups and the Y-SNPs defining them are relevant for the exploration of male lineages, inference of paternal ancestry, and reconstruction of migration pathways, to name a few. Currently, over 300,000 Y-SNPs have been reported, defining 20 main haplogroups. However, ascertainment bias in the investigations has led to some haplogroups being overlooked, which hinders a representative depiction of certain populations and their migration events. For migration pattern analyses of the first settlers of the Americas, the Native American main founding lineage Q-M3 needs to be further investigated to allow clear genetic differentiation of individuals of different ethnogeographic origins. To increase the resolution within this haplogroup, a total of 7.45 Mb of the Y chromosome of 59 admixed South Americans of haplogroup Q was targeted for sequencing using hybridization capture enrichment. Data were combined with 218 publicly available sequences of Central and South Americans of haplogroup Q. After rigorous data processing, variants not meeting the quality criteria were excluded and 4128 reliable Y-SNPs were reported. A total of 2224 Y-SNPs had previously unknown positions in the phylogenetic tree, and 1291 of these are novel. The phylogenetic relationships between the Y-SNPs were established using the software SNPtotree in order to report a redesigned phylogenetic tree containing 300 branches, defined by 3400 Y-SNPs. The new tree introduces 117 previously undescribed branches and is the most comprehensive phylogenetic tree of the Native American haplogroup Q lineages to date. The 214 sequences were assigned to 135 different low- to high-resolution branches, while in the previous phylogenetic tree, only 195 sequences could be sorted into 14 low-resolution branches with the same quality criteria. The improved genetic differentiation of subhaplogroup Q-M3 has a great potential to resolve migration patterns of Native Americans.

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
Human Mutation
Human Mutation 医学-遗传学
CiteScore
8.40
自引率
5.10%
发文量
190
审稿时长
2 months
期刊介绍: Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of novel DNA variations and their phenotypic consequences, reports of SNPs demonstrated as valuable for genomic analysis, descriptions of new molecular detection methods, and novel approaches to clinical diagnosis are welcomed. Novel reports of gene organization at the genomic level, reported in the context of mutation investigation, may be considered. The journal provides a unique forum for the exchange of ideas, methods, and applications of interest to molecular, human, and medical geneticists in academic, industrial, and clinical research settings worldwide.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信