School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Reproductive Medicine Center, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Mol Genet Genomic Med. 2020 Dec;8(12):e1540. doi: 10.1002/mgg3.1540. Epub 2020 Oct 31.
Although glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited disorder in the Chinese population, there is scarce evidence regarding the epidemiology, evolutionary origin, and malaria-induced positive selection effects of G6PD-deficient alleles in various Chinese ethnic populations.
We performed a large population-based screening (n = 15,690) to examine the impact of selection on human nucleotide diversity and to infer the evolutionary history of the most common deficiency alleles in Chinese populations.
The frequencies of G6PD deficiency ranged from 0% to 11.6% in 12 Chinese ethnic populations. A frequency map based on geographic information showed that G6PD deficiency was highly correlated with historical malaria prevalence in China and was affected by altitude and latitude. The five most frequently occurring G6PD gene variants were NM_001042351.3:c.1376G>T, NM_001042351.3:c.1388G>A, NM_001042351.3:c.95A>G, NM_001042351.3:c.1311T>C, and NM_001042351.3:c.1024C>T, which were distributed with ethnic features. A pathogenic but rarely reported variant site (NM_001042351.3:c.448G>A) was identified in this study. Bioinformatic analysis revealed a strong and recent positive selection targeting the NM_001042351.3:c.1376G>T allele that originated in the past 3125 to 3750 years and another selection targeting the NM_001042351.3:c.1388G>A allele that originated in the past 5000 to 6000 years. Additionally, both alleles originated from a single ancestor.
These results indicate that malaria has had a major impact on the Chinese genome since the introduction of rice agriculture.
葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症是中国人群中最常见的遗传性疾病,但关于中国各民族人群中 G6PD 缺乏等位基因的流行病学、进化起源和疟疾诱导的阳性选择效应,证据仍然匮乏。
我们进行了一项大规模的基于人群的筛查(n=15690),以检查选择对人类核苷酸多样性的影响,并推断中国人群中最常见的缺陷等位基因的进化历史。
12 个中国民族群体中 G6PD 缺乏症的频率范围为 0%至 11.6%。基于地理信息的频率图表明,G6PD 缺乏症与中国历史上疟疾的流行高度相关,并且受海拔和纬度的影响。最常发生的 5 种 G6PD 基因突变是 NM_001042351.3:c.1376G>T、NM_001042351.3:c.1388G>A、NM_001042351.3:c.95A>G、NM_001042351.3:c.1311T>C 和 NM_001042351.3:c.1024C>T,这些突变具有民族特征。本研究还鉴定了一个致病性但很少报道的突变位点(NM_001042351.3:c.448G>A)。生物信息学分析显示,针对 NM_001042351.3:c.1376G>T 等位基因的强烈且近期的阳性选择,该等位基因起源于过去 3125 至 3750 年,另一个针对 NM_001042351.3:c.1388G>A 等位基因的选择起源于过去 5000 至 6000 年。此外,这两个等位基因都起源于一个共同的祖先。
这些结果表明,自水稻农业引入以来,疟疾对中国人的基因组产生了重大影响。