Transposable element-mediated balancing selection at Hsp90 underlies embryo developmental variation
Transposable element-mediated balancing selection at Hsp90 underlies embryo developmental variation
复制标题
Hsp90 转座元件介导的平衡选择是胚胎发育变异的基础
DOI:
10.1093/molbev/msx062
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发表时间:
2017
影响因子:
10.7
通讯作者:
Le Kang
中科院分区:
文献类型:
--
作者:
Bing Chen;Bo Zhang;Lingling Xu;Qing Li;Feng Jiang;Pengcheng Yang;Yanan Xu;Le Kang
Understanding the roles of transposable elements (TEs) in the evolution of genome and adaptation is a long-sought goal. Here, we present a new model of TE co-option, in which a TE is harnessed by an essential gene and confers local adaptation through heterozygote advantage. We characterized a humanAlu-like TE family, theLm1elements, in the genome of the migratory locustLocusta migratoriathat harbors 0.7 million copies of the elements. ScanningLm1insertions in the natural locust populations revealed the widespread high polymorphism ofLm1. AnLm1was recruited into the coding region of Heat-shock protein 90 (Hsp90), an important molecular chaperone for diverse signal transduction and developmental pathways. Only heterozygotes of the allele are present in natural populations. Allele frequency increases with decreased latitudes in east coastal China, even increasing up to 76% in southern populations. Regions flanking theLm1insertion display clear signatures of a selective sweep linked toLm1. TheLm1-mediatedHsp90mutation is consequential for the embryonic development of locust. Heterozygous embryos develop faster than the wild type, particularly when cued by long-day parental photoperiod. The heterozygotes also present a reduced within-population variation in embryonic development, i.e., high developmental synchrony of embryos. The naturally occurringHsp90mutation could facilitate multivoltinism and developmental synchronization of the locust in southern tropical region. These results revealed a genetic mechanism behind microevolutionary changes in which balancing selection may have acted to maintain the heterozygote advantage through TE co-option in essential genes.