Verscheure Sophie, Backeljau Thierry, Desmyter Stijn
National Institute of Criminalistics and Criminology, Vilvoordsesteenweg 100, 1120, Brussels, Belgium,
Int J Legal Med. 2015 Sep;129(5):927-35. doi: 10.1007/s00414-014-1106-x. Epub 2014 Nov 14.
Previously, the mitochondrial control region of 214 Belgian dogs was sequenced. Analysis of this data indicated length heteroplasmy of the polyT stretch in the polyC-polyT-polyC stretch from positions 16661 to 16674. Nine polyC-polyT-polyC haplotype combinations were observed, consisting of seven major haplotypes (highest signal intensity) combined with minor haplotypes (lower signal intensity) one T shorter than the major haplotype in all but three dogs. The longer the polyT stretch, the smaller was the difference in signal intensity between the major and minor haplotype peaks. Additional sequencing, cloning, and PCR trap experiments were performed to further study the intra-individual variation of this mitochondrial DNA (mtDNA) region. Cloning experiments demonstrated that the proportion of clones displaying the minor haplotypes also increased with the length of the polyT stretch. Clone amplification showed that in vitro polymerase errors might contribute to the length heteroplasmy of polyT stretches with at least 10 Ts. Although major and minor polyC-polyT-polyC haplotypes did not differ intra-individually within and between tissues in this study, interpretation of polyT stretch variation should be handled with care in forensic casework.
此前,对214只比利时犬的线粒体控制区进行了测序。对该数据的分析表明,在16661至16674位的聚C - 聚T - 聚C序列中,聚T序列存在长度异质性。观察到9种聚C - 聚T - 聚C单倍型组合,由7种主要单倍型(信号强度最高)与次要单倍型(信号强度较低)组成,除三只犬外,次要单倍型比主要单倍型短一个T。聚T序列越长,主要和次要单倍型峰之间的信号强度差异越小。进行了额外的测序、克隆和PCR捕获实验,以进一步研究该线粒体DNA(mtDNA)区域的个体内变异。克隆实验表明,显示次要单倍型的克隆比例也随着聚T序列长度的增加而增加。克隆扩增表明,体外聚合酶错误可能导致至少有10个T的聚T序列的长度异质性。尽管在本研究中,主要和次要聚C - 聚T - 聚C单倍型在组织内和组织间的个体内并无差异,但在法医案件工作中,对聚T序列变异的解释应谨慎处理。