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全染色体单核苷酸多态性揭示了恶性疟原虫的古老起源。

Chromosome-wide SNPs reveal an ancient origin for Plasmodium falciparum.

作者信息

Mu Jianbing, Duan Junhui, Makova Kateryna D, Joy Deirdre A, Huynh Chuong Q, Branch Oralee H, Li Wen-Hsiung, Su Xin-Zhuan

机构信息

Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0425, USA.

出版信息

Nature. 2002 Jul 18;418(6895):323-6. doi: 10.1038/nature00836.

Abstract

The Malaria's Eve hypothesis, proposing a severe recent population bottleneck (about 3,000-5,000 years ago) of the human malaria parasite Plasmodium falciparum, has prompted a debate about the origin and evolution of the parasite. The hypothesis implies that the parasite population is relatively homogeneous, favouring malaria control measures. Other studies, however, suggested an ancient origin and large effective population size. To test the hypothesis, we analysed single nucleotide polymorphisms (SNPs) from 204 genes on chromosome 3 of P. falciparum. We have identified 403 polymorphic sites, including 238 SNPs and 165 microsatellites, from five parasite clones, establishing chromosome-wide haplotypes and a dense map with one polymorphic marker per approximately 2.3 kilobases. On the basis of synonymous SNPs and non-coding SNPs, we estimate the time to the most recent common ancestor to be approximately 100,000-180,000 years, significantly older than the proposed bottleneck. Our estimated divergence time coincides approximately with the start of human population expansion, and is consistent with a genetically complex organism able to evade host immunity and other antimalarial efforts.

摘要

疟疾前夕假说提出,人类疟原虫恶性疟原虫近期经历了严重的种群瓶颈(约3000 - 5000年前),这引发了关于该寄生虫起源和进化的争论。该假说意味着寄生虫种群相对同质化,有利于疟疾控制措施。然而,其他研究表明其起源古老且有效种群规模较大。为了验证这一假说,我们分析了恶性疟原虫3号染色体上204个基因的单核苷酸多态性(SNP)。我们从五个寄生虫克隆中鉴定出403个多态性位点,包括238个SNP和165个微卫星,构建了全染色体单倍型和一个密集图谱,大约每2.3千碱基有一个多态性标记。基于同义SNP和非编码SNP,我们估计最近共同祖先的时间约为100,000 - 180,000年,远早于所提出的瓶颈时间。我们估计的分歧时间大致与人类种群扩张的开始时间相符,并且与一种能够逃避宿主免疫和其他抗疟努力的基因复杂生物体一致。

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