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Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions

The application of X-chromosomal short tandem repeats (X-STRs) has been recognized as a powerful tool in complex kinship testing. To support further development of X-STR analysis in forensic use, we identified nine novel X-STRs, which could be clustered into three linkage groups on Xp21.1, Xq21.31,...

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Autores principales: Yang, Qinrui, Qian, Jinglei, Shao, Chengchen, Yao, Yining, Zhou, Zhihan, Xu, Hongmei, Tang, Qiqun, Qian, Xiaoqin, Xie, Jianhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635773/
https://www.ncbi.nlm.nih.gov/pubmed/34868274
http://dx.doi.org/10.3389/fgene.2021.784605
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author Yang, Qinrui
Qian, Jinglei
Shao, Chengchen
Yao, Yining
Zhou, Zhihan
Xu, Hongmei
Tang, Qiqun
Qian, Xiaoqin
Xie, Jianhui
author_facet Yang, Qinrui
Qian, Jinglei
Shao, Chengchen
Yao, Yining
Zhou, Zhihan
Xu, Hongmei
Tang, Qiqun
Qian, Xiaoqin
Xie, Jianhui
author_sort Yang, Qinrui
collection PubMed
description The application of X-chromosomal short tandem repeats (X-STRs) has been recognized as a powerful tool in complex kinship testing. To support further development of X-STR analysis in forensic use, we identified nine novel X-STRs, which could be clustered into three linkage groups on Xp21.1, Xq21.31, and Xq23. A multiplex PCR system was built based on the electrophoresis. A total of 198 unrelated Shanghai Han samples along with 168 samples from 43 families was collected to investigate the genetic polymorphism and forensic parameters of the nine loci. Allele numbers ranged from 5 to 12, and amplicon sizes ranged from 146 to 477 bp. The multiplex showed high values for the combined power of discrimination (0.99997977 in males and 0.99999999 in females) and combined mean exclusion chances (0.99997918 and 0.99997821 in trios, 0.99984939 in duos, and 0.99984200 in deficiency cases). The linkage between all pairs of loci was estimated via Kosambi mapping function and linkage disequilibrium test, and further investigated through the family study. The data from 43 families strongly demonstrated an independent transmission between LGs and a tight linkage among loci within the same LG. All these results support that the newly described X-STRs and the multiplex system are highly promising for further forensic use.
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spelling pubmed-86357732021-12-02 Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions Yang, Qinrui Qian, Jinglei Shao, Chengchen Yao, Yining Zhou, Zhihan Xu, Hongmei Tang, Qiqun Qian, Xiaoqin Xie, Jianhui Front Genet Genetics The application of X-chromosomal short tandem repeats (X-STRs) has been recognized as a powerful tool in complex kinship testing. To support further development of X-STR analysis in forensic use, we identified nine novel X-STRs, which could be clustered into three linkage groups on Xp21.1, Xq21.31, and Xq23. A multiplex PCR system was built based on the electrophoresis. A total of 198 unrelated Shanghai Han samples along with 168 samples from 43 families was collected to investigate the genetic polymorphism and forensic parameters of the nine loci. Allele numbers ranged from 5 to 12, and amplicon sizes ranged from 146 to 477 bp. The multiplex showed high values for the combined power of discrimination (0.99997977 in males and 0.99999999 in females) and combined mean exclusion chances (0.99997918 and 0.99997821 in trios, 0.99984939 in duos, and 0.99984200 in deficiency cases). The linkage between all pairs of loci was estimated via Kosambi mapping function and linkage disequilibrium test, and further investigated through the family study. The data from 43 families strongly demonstrated an independent transmission between LGs and a tight linkage among loci within the same LG. All these results support that the newly described X-STRs and the multiplex system are highly promising for further forensic use. Frontiers Media S.A. 2021-11-17 /pmc/articles/PMC8635773/ /pubmed/34868274 http://dx.doi.org/10.3389/fgene.2021.784605 Text en Copyright © 2021 Yang, Qian, Shao, Yao, Zhou, Xu, Tang, Qian and Xie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Yang, Qinrui
Qian, Jinglei
Shao, Chengchen
Yao, Yining
Zhou, Zhihan
Xu, Hongmei
Tang, Qiqun
Qian, Xiaoqin
Xie, Jianhui
Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
title Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
title_full Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
title_fullStr Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
title_full_unstemmed Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
title_short Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
title_sort identification and characterization of nine novel x-chromosomal short tandem repeats on xp21.1, xq21.31, and xq23 regions
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635773/
https://www.ncbi.nlm.nih.gov/pubmed/34868274
http://dx.doi.org/10.3389/fgene.2021.784605
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