Thangaraj Kumarasamy, Chaubey Gyaneshwer, Kivisild Toomas, Selvi Rani Deepa, Singh Vijay Kumar, Ismail Thanseem, Carvalho-Silva Denise, Metspalu Mait, Bhaskar L V K S, Reddy Alla G, Chandra Sarat, Pande Veena, Prathap Naidu B, Adarsh Niharika, Verma Abhilasha, Jyothi Inaganti Amara, Mallick Chandana Basu, Shrivastava Nidhi, Devasena Ragala, Kumari Babita, Singh Amit Kumar, Dwivedi Shailendra Kumar Dhar, Singh Shefali, Rao Geeta, Gupta Pranav, Sonvane Vartika, Kumari Kavita, Basha Afsar, Bhargavi K R, Lalremruata Albert, Gupta Arvind Kumar, Kaur Gurukamal, Reddy K K, Rao A Papa, Villems Richard, Tyler-Smith Chris, Singh Lalji
Centre for Cellular and Molecular Biology, Hyderabad, India.
Hum Hered. 2008;66(1):1-9. doi: 10.1159/000114160. Epub 2008 Jan 28.
We have analyzed 7,137 samples from 125 different caste, tribal and religious groups of India and 99 samples from three populations of Nepal for the length variation in the COII/tRNA(Lys) region of mtDNA. Samples showing length variation were subjected to detailed phylogenetic analysis based on HVS-I and informative coding region sequence variation. The overall frequencies of the 9-bp deletion and insertion variants in South Asia were 1.9 and 0.6%, respectively. We have also defined a novel deep-rooting haplogroup M43 and identified the rare haplogroup H14 in Indian populations carrying the 9-bp deletion by complete mtDNA sequencing. Moreover, we redefined haplogroup M6 and dissected it into two well-defined subclades. The presence of haplogroups F1 and B5a in Uttar Pradesh suggests minor maternal contribution from Southeast Asia to Northern India. The occurrence of haplogroup F1 in the Nepalese sample implies that Nepal might have served as a bridge for the flow of eastern lineages to India. The presence of R6 in the Nepalese, on the other hand, suggests that the gene flow between India and Nepal has been reciprocal.
我们分析了来自印度125个不同种姓、部落和宗教群体的7137份样本,以及来自尼泊尔三个群体的99份样本,以研究线粒体DNA(mtDNA)的COII/tRNA(Lys)区域的长度变异。对显示长度变异的样本基于高变区I(HVS-I)和信息编码区序列变异进行了详细的系统发育分析。南亚9碱基缺失和插入变异的总体频率分别为1.9%和0.6%。我们还定义了一个新的深根单倍群M43,并通过完整的mtDNA测序在携带9碱基缺失的印度人群体中鉴定出罕见的单倍群H14。此外,我们重新定义了单倍群M6,并将其分为两个明确的亚分支。北方邦存在单倍群F1和B5a,表明东南亚对印度北部有少量母系遗传贡献。尼泊尔样本中出现单倍群F1意味着尼泊尔可能曾是东部谱系流入印度的桥梁。另一方面,尼泊尔人中有R6表明印度和尼泊尔之间的基因流动是相互的。