Lynn Miriam A, McMaster W Robert
Immunity and Infection Research Centre, Vancouver Coastal Health Institute, and the Department of Medical Genetics, University of British Columbia, 2660 Oak Street, Vancouver, V6H 3Z6 BC, Canada.
Trends Parasitol. 2008 Mar;24(3):103-5. doi: 10.1016/j.pt.2007.11.006. Epub 2008 Feb 5.
The landmark completion of the Leishmania major genome sequence and the recent publication of the L. infantum and L. braziliensis genomes revealed the surprising result that, although separated by 15-50 million years of evolution, the Leishmania genomes are highly conserved and have less than 1% species-specific genes. Yet, these three species of Leishmania cause distinctive and diverse diseases in humans. Here, we discuss these findings together with recent microarray and proteomics studies and highlight their importance in understanding Leishmania disease phenotypes.
硕大利什曼原虫基因组序列的标志性完成以及近期婴儿利什曼原虫和巴西利什曼原虫基因组的发表揭示了一个惊人的结果,即尽管经历了1500万至5000万年的进化分离,但利什曼原虫的基因组高度保守,物种特异性基因不到1%。然而,这三种利什曼原虫在人类中会引发独特且多样的疾病。在此,我们结合近期的微阵列和蛋白质组学研究来讨论这些发现,并强调它们在理解利什曼原虫疾病表型方面的重要性。