Department of Biological Anthropology, Leverhulme Centre for Human Evolutionary Studies, University of Cambridge, Cambridge, United Kingdom.
Mol Biol Evol. 2012 Jan;29(1):249-60. doi: 10.1093/molbev/msr190. Epub 2011 Aug 11.
Milk consumption and lactose digestion after weaning are exclusively human traits made possible by the continued production of the enzyme lactase in adulthood. Multiple independent mutations in a 100-bp region--part of an enhancer--approximately 14-kb upstream of the LCT gene are associated with this trait in Europeans and pastoralists from Saudi Arabia and Africa. However, a single mutation of purported western Eurasian origin accounts for much of observed lactase persistence outside Africa. Given the high levels of present-day milk consumption in India, together with archaeological and genetic evidence for the independent domestication of cattle in the Indus valley roughly 7,000 years ago, we sought to determine whether lactase persistence has evolved independently in the subcontinent. Here, we present the results of the first comprehensive survey of the LCT enhancer region in south Asia. Having genotyped 2,284 DNA samples from across the Indian subcontinent, we find that the previously described west Eurasian -13910 C>T mutation accounts for nearly all the genetic variation we observed in the 400- to 700-bp LCT regulatory region that we sequenced. Geography is a significant predictor of -13910*T allele frequency, and consistent with other genomic loci, its distribution in India follows a general northwest to southeast declining pattern, although frequencies among certain neighboring populations vary substantially. We confirm that the mutation is identical by descent to the European allele and is associated with the same>1 Mb extended haplotype in both populations.
断奶后牛奶的摄入和乳糖消化是人类特有的,这得益于成年后乳糖酶的持续产生。在欧洲人和来自沙特阿拉伯和非洲的牧民中,大约 14kb 上游的 LCT 基因的 100bp 区域的一个增强子的一部分,有多个独立的突变与这一特征相关。然而,一个据称起源于西欧亚的单一突变解释了非洲以外观察到的大部分乳糖持续存在现象。鉴于目前印度的牛奶消费水平很高,以及印度河流域大约 7000 年前牛独立驯化的考古和遗传证据,我们试图确定乳糖持续存在是否在该次大陆独立进化。在这里,我们首次全面调查了南亚的 LCT 增强子区域。通过对来自印度次大陆各地的 2284 个 DNA 样本进行基因分型,我们发现,之前描述的欧亚西部-13910C>T 突变几乎解释了我们在 400-700bp 的 LCT 调控区域中观察到的所有遗传变异,我们对该区域进行了测序。地理是-13910*T 等位基因频率的一个重要预测因子,与其他基因组位点一致,它在印度的分布遵循从西北到东南逐渐下降的模式,尽管某些相邻人群的频率有很大差异。我们证实,该突变与欧洲等位基因相同,并且与两个群体中相同的>1Mb 扩展单倍型相关。