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Y-STRs and AZF microdeletions in clinical context samples

机译:临床背景样本中的Y-STR和AZF微缺失

摘要

Forensic geneticists use several Y-STR PCR amplification kits, which are useful in forensic identification, ancestry studies and genealogies reconstruction. The Y-chromosome regions with forensic interest include the set of 16 loci defined in the Y-Chromosome Haplotype Reference Database. Nevertheless Y chromosome is connected to male infertility and microdeletions in it are the most common cause of genetic origin male infertility. The study of Y chromosome AZF (Azoospermic Factor) region is one of the strategies to diagnose it. This study aimed to characterize the AZF region microdeletions by Y-STRs and STS studies and its possible impact in forensic casework. Selected samples from fifty-two patients studied for male infertility, collected under informed consent, were characterized at molecular level with specific STS for the presence/absence of the three AZF regions: AZFa – DFFRY3, DBY; AZFb – sY1227, sY1224, sY134, sY119, sY134, RBMY1, sY143; AZFc – sY1192, sY254, RRM3, sY1291, sY283, sY1201. AmpFℓSTR® Yfiler® PCR Amplification® kit (AB) was used to obtain a 16 Y-STR profile. All the 52 samples were concordant in forensic and molecular studies, although with different scenarios: a) a normal Y-STR profile and no deletion with STS in the AZF region were revealed in about 32% of the studied samples; b) the majority of samples, about 51%, revealed also a normal Y-STR profile, but with a complete or partial deletion(1 or 2 STS) in the AZFc region; c) deletion in DYS385, DYS392, DYS448 and in AZFb+AZFc were detected in 3 samples. Four samples have the following different scenarios: d) deletion in DYS385, DYS392, DYS448 and in AZFb; e) deletion in DYS390, DYS391, DYS392, DYS385, DYS438, DYS439, DYS458, DYS635 and in AZFa; f) deletion in DYS448, in STS sY1197 and in AZFc; g) deletion in DYS390, DYS392, DYS385, DYS448, GATAH4 and in AZFb+AZFc region. All Y-STRs studied for forensic casework are localized, essentially, in the AZFa or AZFb regions, although DYS448 is located in the distal AZFb region and DYS390 and GATAH4 are localized between AZFa and AZFb regions. Deletion in the AZFc region does not affect results in forensics.The knowledge of Y-chromossome microdeletions is important in Forensic Genetics as this can be encountered in current casework without possibility to perform clinical studies. So, it is crucial to know how to interpret the results obtained in Y-STR microdeletions samples, according to Y-chromossome structural alterations. As Y-STRs used in Forensic Genetic Laboratories are located in the AZF region, associated to male infertility, this can raise some ethical problems in Forensics.
机译:法医遗传学家使用几种Y-STR PCR扩增试剂盒,可用于法医鉴定,血统研究和家谱重建。具有法医学意义的Y染色体区域包括Y染色体单倍型参考数据库中定义的16个基因座的集合。然而,Y染色体与男性不育有关,其中的微小缺失是遗传上男性不育的最常见原因。 Y染色体AZF(无精子因子)区域的研究是诊断它的策略之一。这项研究旨在通过Y-STR和STS研究来表征AZF区域的微缺失及其对法医案件的可能影响。在知情同意下收集了来自52位研究男性不育症患者的样本,并在分子水平上用特异的STS对三个AZF区域的存在/不存在进行了表征:AZFa – DFFRY3,DBY; AZFb – sY1227,sY1224,sY134,sY119,sY134,RBMY1,sY143; AZFc – sY1192,sY254,RRM3,sY1291,sY283,sY1201。使用AmpFABSTR®Yfiler®PCRAmplification®试剂盒(AB)获得16 Y-STR谱图。尽管在不同的情况下,所有52个样本在法医和分子研究中都是一致的:a)约32%的样本中显示正常的Y-STR谱图和AZF区中STS的缺失。 b)大多数样品(约51%)也显示出正常的Y-STR谱,但在AZFc区有完整或部分缺失(1或2个STS); c)在3个样品中检测到DYS385,DYS392,DYS448和AZFb + AZFc中的缺失。四个样本具有以下不同情况:d)在DYS385,DYS392,DYS448和AZFb中删除; e)在DYS390,DYS391,DYS392,DYS385,DYS438,DYS439,DYS458,DYS635和AZFa中删除; f)在DYS448,STS sY1197和AZFc中缺失; g)在DYS390,DYS392,DYS385,DYS448,GATAH4和AZFb + AZFc区域中缺失。尽管DYS448位于AZFb的远端区域,而DYS390和GATAH4则位于AZFa和AZFb区域之间,但所有为法医案例研究的Y-STR基本上都位于AZFa或AZFb区域。 AZFc区的缺失不会影响法医学的结果。Y染色体微缺失的知识在法医遗传学中很重要,因为在当前案例研究中可能会遇到这种情况,而无法进行临床研究。因此,至关重要的是要知道如何根据Y染色体结构的变化来解释Y-STR微缺失样品中获得的结果。由于法医遗传实验室中使用的Y-STR位于与男性不育症相关的AZF地区,因此这可能会引起法医方面的一些伦理问题。

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