Department of Entomology, Virginia Polytechnic and State University, West Campus Drive, Blacksburg, VA 24061, USA.
Parasit Vectors. 2011 Oct 19;4:202. doi: 10.1186/1756-3305-4-202.
Anopheles nili is a major vector of malaria in the humid savannas and forested areas of sub-Saharan Africa. Understanding the population genetic structure and evolutionary dynamics of this species is important for the development of an adequate and targeted malaria control strategy in Africa. Chromosomal inversions and microsatellite markers are commonly used for studying the population structure of malaria mosquitoes. Physical mapping of these markers onto the chromosomes further improves the toolbox, and allows inference on the demographic and evolutionary history of the target species.
Availability of polytene chromosomes allowed us to develop a map of microsatellite markers and to study polymorphism of chromosomal inversions. Nine microsatellite markers were mapped to unique locations on all five chromosomal arms of An. nili using fluorescent in situ hybridization (FISH). Probes were obtained from 300-483 bp-long inserts of plasmid clones and from 506-559 bp-long fragments amplified with primers designed using the An. nili genome assembly generated on an Illumina platform. Two additional loci were assigned to specific chromosome arms of An. nili based on in silico sequence similarity and chromosome synteny with Anopheles gambiae. Three microsatellites were mapped inside or in the vicinity of the polymorphic chromosomal inversions 2Rb and 2Rc. A statistically significant departure from Hardy-Weinberg equilibrium, due to a deficit in heterozygotes at the 2Rb inversion, and highly significant linkage disequilibrium between the two inversions, were detected in natural An. nili populations collected from Burkina Faso.
Our study demonstrated that next-generation sequencing can be used to improve FISH for microsatellite mapping in species with no reference genome sequence. Physical mapping of microsatellite markers in An. nili showed that their cytological locations spanned the entire five-arm complement, allowing genome-wide inferences. The knowledge about polymorphic inversions and chromosomal locations of microsatellite markers has been useful for explaining differences in genetic variability across loci and significant differentiation observed among natural populations of An. nili.
黑足按蚊是撒哈拉以南非洲湿润稀树草原和森林地区疟疾的主要传播媒介。了解该物种的种群遗传结构和进化动态对于在非洲制定适当和有针对性的疟疾控制策略非常重要。染色体倒位和微卫星标记常用于研究疟蚊的种群结构。这些标记的物理图谱进一步改进了工具包,并允许对目标物种的人口和进化历史进行推断。
多线染色体的可用性使我们能够开发微卫星标记图谱,并研究染色体倒位的多态性。使用荧光原位杂交(FISH)将 9 个微卫星标记映射到黑足按蚊所有 5 条染色体臂的独特位置。探针来自质粒克隆的 300-483 bp 长插入片段和使用 Illumina 平台生成的黑足按蚊基因组组装设计的引物扩增的 506-559 bp 长片段。根据序列相似性和与冈比亚按蚊的染色体同线性,另外两个基因座被分配到黑足按蚊特定的染色体臂上。3 个微卫星标记映射到多态性染色体倒位 2Rb 和 2Rc 内或附近。在来自布基纳法索的天然黑足按蚊种群中,由于 2Rb 倒位杂合子的缺失,以及两个倒位之间的高度显著连锁不平衡,检测到哈迪-温伯格平衡的显著偏离。
我们的研究表明,下一代测序可以用于改进没有参考基因组序列的物种的 FISH 微卫星图谱。黑足按蚊微卫星标记的物理图谱表明,它们的细胞学位置跨越了整个五臂补体,允许进行全基因组推断。关于多态性倒位和微卫星标记染色体位置的知识对于解释不同基因座之间遗传变异性的差异以及在黑足按蚊自然种群中观察到的显著分化非常有用。