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巴基斯坦牙釉蛋白Y基因缺失男性单倍型的多样化。

Diversification of Pakistani Amelogenin-Y-Null Male Haplotypes.

作者信息

Siddique Nasir, Shahid Ahmad Ali, Sughra Kalsoom

机构信息

Department of Biochemistry & Biotechnology, University of Gujrat, Gujrat, Pakistan.

DNA and Serology Section, Punjab Forensic Science Agency, Lahore, Pakistan.

出版信息

Scientifica (Cairo). 2021 May 4;2021:5521411. doi: 10.1155/2021/5521411. eCollection 2021.

Abstract

Amelogenin is a common sex typing marker encountered in forensic case work. Phenotypically normal males have been reported in the literature who exhibit anomalous amelogenin allele. These males express only a single amelogenin peak representing AMEL-X and are called as AMEL-Y-null males. Gender misclassification of such individuals is an obvious consequence of this mutation, as a male sample would falsely appear to be a female sample. This study was aimed to attribute the AMEL-Y-null male DNA profiles encountered in forensic casework in the Pakistani population to appropriate phylogenetic clade based on shared ancestry. A total of 18 null AMEL-Y males were screened out of the sample pool of 5000 male individuals, reflecting mutational frequency of 0.36%. A common phylogenetic ancestor is suggested for 17 individuals, based on computational analysis of the Y-STR haplotypes, shown to be belonging to the J haplogroup while only one sample belonged to the R group. The samples in J groups showed homology with subclades J2b2a M241 and J2b2a PH1648, while R group individual showed 100% homology with R1a. Data are reported after haplotype network development of AMEL-Y-null Pakistani males using Network 10.0 for the study of evolutionary distances and emergence of nodes.

摘要

牙釉蛋白是法医案件工作中常见的性别分型标记物。文献报道过一些表型正常但牙釉蛋白等位基因异常的男性。这些男性仅表达代表AMEL-X的单个牙釉蛋白峰,被称为AMEL-Y缺失男性。这种突变的一个明显后果是此类个体的性别误判,因为男性样本会错误地显示为女性样本。本研究旨在根据共同祖先,将巴基斯坦人群法医案件工作中遇到的AMEL-Y缺失男性DNA图谱归为合适的系统发育分支。在5000名男性个体的样本库中总共筛选出18名AMEL-Y缺失男性,突变频率为0.36%。基于Y-STR单倍型的计算分析,建议17名个体有一个共同的系统发育祖先,显示属于J单倍群,而只有一个样本属于R组。J组的样本与亚分支J2b2a M241和J2b2a PH1648显示出同源性,而R组个体与R1a显示出100%的同源性。在使用Network 10.0对AMEL-Y缺失的巴基斯坦男性进行单倍型网络开发以研究进化距离和节点出现后报告了数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ef/8116151/e1ddbd078fca/SCIENTIFICA2021-5521411.001.jpg

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