Department of Biology, University of Texas at San Antonio, TX 78249, USA.
BMC Genomics. 2010 Dec 1;11 Suppl 3(Suppl 3):S13. doi: 10.1186/1471-2164-11-S3-S13.
The increasing resistance of Plasmodium, the malaria parasites, to multiple commonly used drugs has underscored the urgent need to develop effective antimalarial drugs and vaccines. The new direction of genomics-driven target discovery has become possible with the completion of parasite genome sequencing, which can lead us to a better understanding of how the parasites develop the genetic variability that is associated with their response to environmental challenges and other adaptive phenotypes.
We present the results of a comprehensive analysis of the genomes of six Plasmodium species, including two species that infect humans, one that infects monkeys, and three that infect rodents. The core genome shared by all six species is composed of 3,351 genes, which make up about 22%-65% of the genome repertoire. These components play important roles in fundamental functions as well as in parasite-specific activities. We further investigated the distribution and features of genes that have been expanded in specific Plasmodium lineage(s). Abundant duplicate genes are present in the six species, with 5%-9% of the whole genomes composed lineage specific radiations. The majority of these gene families are hypothetical proteins with unknown functions; a few may have predicted roles such as antigenic variation.
The core genome components in the malaria parasites have functions ranging from fundamental biological processes to roles in the complex networks that sustain the parasite-specific lifestyles appropriate to different hosts. They represent the minimum requirement to maintain a successful life cycle that spans vertebrate hosts and mosquito vectors. Lineage specific expansions (LSEs) have given rise to abundant gene families in Plasmodium. Although the functions of most families remain unknown, these LSEs could reveal components in parasite networks that, by their enhanced genetic variability, can contribute to pathogenesis, virulence, responses to environmental challenges, or interesting phenotypes.
疟原虫(引起疟疾的寄生虫)对多种常用药物的耐药性不断增强,这突显了开发有效抗疟药物和疫苗的迫切需要。随着寄生虫基因组测序的完成,基因组驱动的靶标发现新方向成为可能,这使我们能够更好地了解寄生虫如何产生与它们对环境挑战和其他适应性表型的反应相关的遗传变异性。
我们介绍了对六种疟原虫物种基因组进行全面分析的结果,包括两种感染人类的物种、一种感染猴子的物种和三种感染啮齿动物的物种。所有六种物种共有的核心基因组由 3351 个基因组成,约占基因组库的 22%-65%。这些组成部分在基本功能以及寄生虫特有的活动中发挥着重要作用。我们进一步研究了在特定疟原虫谱系中扩展的基因的分布和特征。在六种物种中都存在丰富的重复基因,整个基因组中有 5%-9%是特定谱系的辐射。这些基因家族中的大多数是具有未知功能的假设蛋白;少数可能具有预测的作用,如抗原变异。
疟原虫核心基因组成分的功能范围从基本的生物过程到维持适合不同宿主的寄生虫特有生活方式的复杂网络中的作用。它们代表了维持跨越脊椎动物宿主和蚊子媒介的成功生命周期的最低要求。谱系特异性扩张(LSE)在疟原虫中产生了丰富的基因家族。尽管大多数家族的功能仍然未知,但这些 LSE 可以揭示寄生虫网络中的成分,通过增强的遗传变异性,有助于发病机制、毒力、对环境挑战的反应或有趣的表型。