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A Molecular Clock for Malaria Parasites

机译:疟疾寄生虫的分子钟

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摘要

The evolutionary origins of new lineages of pathogens are fundamental to understanding emerging diseases. Phylogenetic reconstruction based on DNA sequences has revealed the sister taxa of human pathogens, but the timing of host-switching events, including the human malaria pathogen Plasmodium falciparum, remains controversial. Here, we establish a rate for cytochrome b evolution in avian malaria parasites relative to its rate in birds. We found that the parasite cytochrome b gene evolves about 60% as rapidly as that of host cytochrome b, corresponding to ~1.2% sequence divergence per million years. This calibration puts the origin of P. falciparum at 2.5 million years ago (Ma), the initial radiation of mammalian Plasmodium at 12.8 Ma, and the contemporary global diversity of the Haemosporida across terrestrial vertebrates at 16.2 Ma.
机译:新的病原体谱系的进化起源是了解新兴疾病的基础。基于DNA序列的系统发育重建揭示了人类病原体的姊妹类群,但是包括人类疟疾病原体恶性疟原虫在内的宿主转换事件的发生时间仍然存在争议。在这里,我们建立相对于鸟类疟疾寄生虫中细胞色素b进化的速率。我们发现,寄生虫细胞色素b基因的进化速度约为宿主细胞色素b基因的进化速度的60%,相当于每百万年〜1.2%的序列差异。该校准将恶性疟原虫的起源定为250万年前(Ma),哺乳动物疟原虫的初始辐射为12.8 Ma,当代整个陆地脊椎动物的血孢的全球多样性为16.2 Ma。

著录项

  • 来源
    《Science》 |2010年第5988期|P.226-229|共4页
  • 作者单位

    Department of Biology, University of Missouri-St. Louis, One University Boulevard, St. Louis, MO 63121-4499, USA;

    rnDepartment of Biology, University of Missouri-St. Louis, One University Boulevard, St. Louis, MO 63121-4499, USA Department of Biological Sciences, Mississippi State University, 130 Harned Hall, Lee Boulevard, Mississippi State, MS 39762, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 02:54:34

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