Thangaraj Kumarasamy, Sridhar Vempati, Kivisild Toomas, Reddy Alla G, Chaubey Gyaneshwer, Singh Vijay Kumar, Kaur Suminder, Agarawal Pooja, Rai Amit, Gupta Jalaj, Mallick Chandana Basu, Kumar Niraj, Velavan Thrimulaisamy P, Suganthan Rajanbabu, Udaykumar Divi, Kumar Rashmi, Mishra Rachana, Khan Arif, Annapurna Chitikineni, Singh Lalji
Centre for Cellular and Molecular biology, Uppal Road, Hyderabad, 500 007, India.
Hum Genet. 2005 May;116(6):507-17. doi: 10.1007/s00439-005-1271-6. Epub 2005 Mar 17.
Length variation in the human mtDNA intergenic region between the cytochrome oxidase II (COII) and tRNA lysine (tRNA(lys)) genes has been widely studied in world populations. Specifically, Austronesian populations of the Pacific and Austro-Asiatic populations of southeast Asia most frequently carry the 9-bp deletion in that region implying their shared common ancestry in haplogroup B. Furthermore, multiple independent origins of the 9-bp deletion at the background of other mtDNA haplogroups has been shown in populations of Africa, Europe, Australia, and India. We have analyzed 3293 Indian individuals belonging to 58 populations, representing different caste, tribal, and religious groups, for the length variation in the 9-bp motif. The 9-bp deletion (one copy) and insertion (three copies) alleles were observed in 2.51% (2.15% deletion and 0.36% insertion) of the individuals. The maximum frequency of the deletion (45.8%) was observed in the Nicobarese in association with the haplogroup B5a D-loop motif that is common throughout southeast Asia. The low polymorphism in the D-loop sequence of the Nicobarese B5a samples suggests their recent origin and a founder effect, probably involving migration from southeast Asia. Interestingly, none of the 302 (except one Munda sample, which has 9-bp insertion) from Mundari-speaking Austro-Asiatic populations from the Indian mainland showed the length polymorphism of the 9-bp motif, pointing either to their independent origin from the Mon-Khmeric-speaking Nicobarese or to an extensive admixture with neighboring Indo-European-speaking populations. Consistent with previous reports, the Indo-European and Dravidic populations of India showed low frequency of the 9-bp deletion/insertion. More than 18 independent origins of the deletion or insertion mutation could be inferred in the phylogenetic analysis of the D-loop sequences.
人类线粒体DNA(mtDNA)细胞色素氧化酶II(COII)基因与赖氨酸转运RNA(tRNA(lys))基因之间的基因间隔区长度变异,已在世界各人群中得到广泛研究。具体而言,太平洋地区的南岛语族人群以及东南亚的南亚语族人群在该区域最常携带9碱基对缺失,这意味着他们在单倍群B中有共同的祖先。此外,在非洲、欧洲、澳大利亚和印度的人群中,已发现9碱基对缺失在其他mtDNA单倍群背景下有多个独立起源。我们分析了来自58个群体的3293名印度个体,这些群体代表不同的种姓、部落和宗教群体,以研究9碱基基序的长度变异。在2.51%的个体中观察到9碱基对缺失(一个拷贝)和插入(三个拷贝)等位基因(2.15%为缺失,0.36%为插入)。在尼科巴人中观察到缺失的最高频率(45.8%),且与单倍群B5a D环基序相关,该基序在整个东南亚都很常见。尼科巴人B5a样本D环序列中的低多态性表明其起源较近且存在奠基者效应,可能涉及从东南亚的迁徙。有趣的是,来自印度大陆说蒙达里语的南亚语族群体的302个样本(除了一个有9碱基对插入的蒙达样本)均未显示9碱基基序的长度多态性,这表明要么他们与说孟-高棉语的尼科巴人有独立起源,要么与相邻的说印欧语的群体有广泛的混合。与之前的报道一致,印度的说印欧语和达罗毗荼语的群体中9碱基对缺失/插入的频率较低。在D环序列的系统发育分析中,可以推断出缺失或插入突变有超过18个独立起源。