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首页> 外文期刊>Legal medicine >Abnormal detection of Y-STR alleles at DYS385 from female DNA in forensic casework and interchromosomal insertional translocation of P4 palindrome (HSFY/DYS385) from AZFb region
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Abnormal detection of Y-STR alleles at DYS385 from female DNA in forensic casework and interchromosomal insertional translocation of P4 palindrome (HSFY/DYS385) from AZFb region

机译:来自AZFB区域的法医案例作用中雌性DNA和雌性DNA的雌性DNA的Y-STR等位基因异常检测来自AZFB区域的P4 Parindrome(HSFY / DYS385)的运动学插入易位

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摘要

The unknown origin of DNA samples derived from crime scenes generates a considerable amount of uncertainty, as do unexpected short tandem repeat (STR) results caused by sample mix-ups, contamination, medical interventions, and transgender individuals (broad meaning). Genetic abnormalities such as somatic/germline mutations, mosaicism or chimerism, sex reversal cases, aneuploidies, and chromosomal structural rearrangements are also possible causes of such results. The evidence offered by the present study suggested that additional DYS385 alleles, as seen in mixed stain samples and in the potentially single-source DNA profile of a female, originated from the female DNA source only. For the case reported here, we propose an interchromosomal insertion hypothesis, in which a 768-kb segment including the P4 palindrome of the azoospermia factor (AZFb) region was deleted from the Y chromosome and inserted into the X chromosome or an autosome during male meiosis. Y-SNP data points from the AccuID platform and in-house PCR assays narrowed down the expected length of the target region. Bioinformatics analysis followed by whole genome amplification and whole genome sequencing showed that a 529-kb segment including the P4 palindrome (HSFY/DYS385)/DYS460 region from the female sample mapped to the Y reference sequence (GRCh37). To our knowledge, the interchromosomal insertional translocation event was identified as an unknown type of genomic rearrangement in the forensic genetic field.
机译:源自犯罪现场的DNA样本的未知起源产生了相当大的不确定性,如出乎意料的短串联重复(str)结果,由样本混合物,污染,医疗干预和变性人(广泛的意义)引起。遗传异常,如体细胞/种系突变,镶嵌或嵌合体,性逆转病例,非血糖倍增剂和染色体结构重排也可能是这种结果的可能原因。本研究提供的证据表明,在混合染色样品中看到的额外的DYS385等位基因以及仅来自雌性DNA源的雌性的潜在单源DNA谱。对于此处报告的情况,我们提出了间瘤瘤性插入假设,其中从Y染色体中删除了包括偶氮孢子症(AZFB)区的P4糖蛋白酶(AZFB)区域的768kb段,并在雄性分裂期间插入X染色体或血清体中。来自accuid平台和内部PCR测定的Y-SNP数据点缩小了目标区域的预期长度。生物信息学分析随后全基因组扩增和全基因组测序显示,529-kB段,包括来自映射到Y参考序列(GRCH 37)的雌性样品的P4普林诺(HSFY / DYS385)/ dys460区域。据我们所知,在法医遗传领域中鉴定了间同胞形式插入易位事件作为一种未知类型的基因组重排。

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