Canturk Kemal Murat, Emre Ramazan, Gurkan Cemal, Komur Ilhami, Muslumanoglu Omer, Dogan Muhammed
Department of Biology, Council of Forensic Medicine, Ministry of Justice, Turkey
Department of Biology, Council of Forensic Medicine, Ministry of Justice, Turkey.
Med Sci Law. 2016 Jul;56(3):210-2. doi: 10.1177/0025802415605539. Epub 2015 Sep 16.
Here, we report an incest paternity case involving three biological brothers as alleged fathers (AFs), their biological sister and her child that was investigated using the Investigator ESSplex Plus, AmpFLSTR Identifiler Plus/Investigator IDplex Plus and PowerPlex 16 kits. Initial duo paternity investigations using 15-loci autosomal short tandem repeat (STR) analyses failed to exclude any of the AFs. Despite the fact that one of the brothers, AF1, had a mismatch with the child at a single locus (D2S1338), the possibility of a single-step mutation could not be ruled out. When the number of autosomal STR loci analysed was increased to 22 without the inclusion of the mother, AF2 and AF3 still could not be excluded, since both of them again had no mismatches with the child. A breakthrough was possible only upon inclusion of the mother so that trio paternity investigations were carried out. This time AF1 and AF2 could be excluded at two loci (D2S1338 and D1S1656) and six loci (vWa, D1S1656, D12S391, FGA, PENTA E and PENTA D), respectively, and AF3 was then the only brother who could not be excluded from paternity. Subsequent statistical analyses suggested that AF3 could be the biological father of the child with a combined paternity index >100 billion and a probability of paternity >99.99999999%. These findings consolidate the fact that complex paternity cases such as those involving incest could benefit more from the inclusion of the mother than simply increasing the number of STR loci analysed.
在此,我们报告一例乱伦亲子关系案件,涉及三名亲兄弟作为被指控父亲(AFs),他们的亲姐妹及其孩子,该案件使用Investigator ESSplex Plus、AmpFLSTR Identifiler Plus/Investigator IDplex Plus和PowerPlex 16试剂盒进行了调查。最初使用15个位点的常染色体短串联重复序列(STR)分析进行的二联体亲子关系调查未能排除任何一名被指控父亲。尽管兄弟之一AF1在一个位点(D2S1338)与孩子存在不匹配,但不能排除单步突变的可能性。当分析的常染色体STR位点数量增加到22个且未纳入母亲时,AF2和AF3仍然无法被排除,因为他们两人与孩子均再次不存在不匹配。只有纳入母亲进行三联体亲子关系调查才有可能取得突破。这一次,AF1和AF2分别在两个位点(D2S1338和D1S1656)和六个位点(vWa、D1S1656、D12S391、FGA、PENTA E和PENTA D)被排除,然后AF3是唯一不能被排除亲子关系的兄弟。随后的统计分析表明,AF3可能是孩子的生物学父亲,联合亲权指数>1000亿,亲权概率>99.99999999%。这些发现强化了这样一个事实,即像涉及乱伦的复杂亲子关系案件,纳入母亲比单纯增加分析的STR位点数量更有益。