人指甲内源DNA短串联重复分型研究

Miriam Jasim Shehab
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All samples were typed for fifteen autosomal STR loci along with amelogenin, using the Applied Biosystems AmpFiSTR® IdentifilerTM kit. Our finding showed that input of 5 mg nail material (1 to 2 of fingernail clippings) gives a variable yield of DNA concentration also there was no significant difference in The mean of concentration for samples that isolated from whole fingernail and those isolated from fingernail after cut into small pieces for children groups while there were significant difference for adult and adolescent groups (0.107702, 0.07544 and 0.000192 respectively). Also the allele’s percentage of STR profiles for three age groups was fluctuated among (100, 33.3, 53.3, 66.6, 73.3, 86.6, and 93.3%). [DOI: 10.22401/JUNS.21.1.16] Keyword: Genomic DNA, Fingernail, DNA analysis, Allele percentage, STR profile. Introduction Deoxyribonucleic acid (DNA) profiling is an effective technique for human identification and/ or the resolution of criminal and civil legal disputes. 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Many studies have confirmed that nails are suitable for analysis [21-23], but their use as a provenance of DNA in the forensic field is rather rare. The aim of the present study was to verify whether human nails are appropriate for personal identification and paternity testing. Materials and Methods Samples Thirty fresh human fingernails were obtained from random volunteers an age average (8-60). Thirty buccal swabs were also collected from same volunteers and used as reference samples. Fingernails were subjected to two different treatments. In the first treatment DNA was isolated from whole fingernail clipping while in the second treatment fingernail clipping was cut into small pieces to increase surface area exposed to lysis solution. DNA Extraction DNA was extracted from fingernail samples using organically after a modification of a previously published protocol [21] and buccal swab samples were extracted according to Souvik et.al. 2013 [24]. 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引用次数: 0

摘要

基因组DNA是从不同的生物来源分离出来的。指甲含有基因组DNA,但由于指甲组织的特殊组成和结构,DNA嵌入角化细胞中,因此从指甲组织中分离遗传物质受到限制。本研究旨在探讨从指甲中分离的DNA在法医分析中的应用能力。从三组(10个儿童指甲样本,10个青少年指甲样本和10个成人指甲样本)中收集30个剪指甲样本,并从同一组志愿者中收集30个口腔拭子样本作为参考样本。指甲修剪和口腔拭子均采用苯酚/氯仿萃取法提取DNA。使用Applied Biosystems AmpFiSTR®IdentifilerTM试剂盒,对所有样本进行15个常染色体STR位点和淀粉原蛋白分型。结果表明,5 mg指甲材料(1 ~ 2个指甲剪)的输入量可以产生不同的DNA浓度,儿童组的全指甲分离样品和切成小块的指甲分离样品的平均浓度无显著差异,成人组和青少年组的平均浓度差异显著(分别为0.107702、0.07544和0.000192)。3个年龄组STR等位基因比例在100、33.3、53.3、66.6、73.3、86.6、93.3%之间波动。[DOI: 10.22401/ june .21.1.16]关键词:基因组DNA,指甲,DNA分析,等位基因百分比,STR谱。脱氧核糖核酸(DNA)分析是人类身份识别和/或解决刑事和民事法律纠纷的有效技术。DNA分析的一个重要特点是它可以用于各种生物来源的分类。这些来源包括血液[1,2]、精液[3]、毛发[4-6]、唾液[7]、骨骼[8-14]和牙齿[1517]。用短串联重复序列(STR)标记对个体进行DNA分析是法医遗传学和亲子鉴定中常用的方法。短串联重复序列是用于法医鉴定的DNA非编码区域,因为在这些区域发现的个体之间存在差异[18]。它们约占人类基因组的3%,每10000个核苷酸中出现一次[19]。指甲、头发、角和羽毛(角质组织)已被用作遗传物质的来源超过20年。使用角状组织有一些特别的好处,包括易于获得样品和这些组织中DNA的相对稳定性[20]。许多研究证实,指甲适合用于分析[21-23],但在法医领域将其用作DNA来源的情况相当罕见。本研究的目的是验证人的指甲是否适合于个人鉴定和亲子鉴定。材料与方法样本随机抽取年龄在8-60岁的志愿者30个新鲜指甲。还从同一志愿者身上收集了30份口腔拭子作为参考样本。指甲受到两种不同的处理。在第一种处理中,DNA从整个指甲剪中分离出来,而在第二种处理中,指甲剪被切成小块,以增加暴露于溶解溶液的表面积。DNA提取对先前发表的方案进行修改后,采用有机方法从指甲样本中提取DNA[21],并根据Souvik等人的方法提取口腔拭子样本。2013[24]。移除
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Short Tandem Repeat Typing Using Endogenous DNA Isolated from Human Fingernail
Genomic DNA was isolated from variable biological sources. Nails contain genomic DNA but there is limitation in isolating of genetic material from this tissue due to the special composition and structure of this tissue in which DNA embedded in keratinized cells. This study aimed to investigate the capability of using DNA that isolated from fingernails in forensic analysis. Thirty fingernails clipping were collected from three groups (10 fingernail samples for children, 10 fingernail samples for adolescent and 10 fingernail samples for adult) in addition to thirty buccal swabs collected from the same volunteers as reference samples. Both fingernail clipping and buccal swabs were subjected to DNA extraction using phenol/chloroform extraction. All samples were typed for fifteen autosomal STR loci along with amelogenin, using the Applied Biosystems AmpFiSTR® IdentifilerTM kit. Our finding showed that input of 5 mg nail material (1 to 2 of fingernail clippings) gives a variable yield of DNA concentration also there was no significant difference in The mean of concentration for samples that isolated from whole fingernail and those isolated from fingernail after cut into small pieces for children groups while there were significant difference for adult and adolescent groups (0.107702, 0.07544 and 0.000192 respectively). Also the allele’s percentage of STR profiles for three age groups was fluctuated among (100, 33.3, 53.3, 66.6, 73.3, 86.6, and 93.3%). [DOI: 10.22401/JUNS.21.1.16] Keyword: Genomic DNA, Fingernail, DNA analysis, Allele percentage, STR profile. Introduction Deoxyribonucleic acid (DNA) profiling is an effective technique for human identification and/ or the resolution of criminal and civil legal disputes. One force characteristic of DNA profiling is that it may be used in assortment of various biological sources. Some of these sources include blood [1,2], semen[3], hair[4-6], saliva[7],bone[8-14] and teeth [1517]. DNA profiling of individuals with short tandem repeat (STR) markers is commonly used in forensic genetics and paternity testing. Short tandem repeats are non-coding regions of DNA used for forensic identification due to the variation between individual found in these regions [18]. They occupy about 3% of the human genome and occur on every 10,000 nucleotides [19]. Nail, hair, horn and feather (keratinous tissues) have been utilized as a source of genetic material for over 20 years. There are particular benefits of using keratinous tissues include the ease obtaining of the sample and the relative stability of DNA in these tissues [20]. Many studies have confirmed that nails are suitable for analysis [21-23], but their use as a provenance of DNA in the forensic field is rather rare. The aim of the present study was to verify whether human nails are appropriate for personal identification and paternity testing. Materials and Methods Samples Thirty fresh human fingernails were obtained from random volunteers an age average (8-60). Thirty buccal swabs were also collected from same volunteers and used as reference samples. Fingernails were subjected to two different treatments. In the first treatment DNA was isolated from whole fingernail clipping while in the second treatment fingernail clipping was cut into small pieces to increase surface area exposed to lysis solution. DNA Extraction DNA was extracted from fingernail samples using organically after a modification of a previously published protocol [21] and buccal swab samples were extracted according to Souvik et.al. 2013 [24]. To remove the
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