Indjeian Vahan B, Kingman Garrett A, Jones Felicity C, Guenther Catherine A, Grimwood Jane, Schmutz Jeremy, Myers Richard M, Kingsley David M
Howard Hughes Medical Institute; Stanford University School of Medicine, Department of Developmental Biology, 279 Campus Drive, Beckman Center B300, Stanford, CA 94305, USA.
Stanford University School of Medicine, Department of Developmental Biology, 279 Campus Drive, Beckman Center B300, Stanford, CA 94305, USA.
Cell. 2016 Jan 14;164(1-2):45-56. doi: 10.1016/j.cell.2015.12.007. Epub 2016 Jan 7.
Changes in bone size and shape are defining features of many vertebrates. Here we use genetic crosses and comparative genomics to identify specific regulatory DNA alterations controlling skeletal evolution. Armor bone-size differences in sticklebacks map to a major effect locus overlapping BMP family member GDF6. Freshwater fish express more GDF6 due in part to a transposon insertion, and transgenic overexpression of GDF6 phenocopies evolutionary changes in armor-plate size. The human GDF6 locus also has undergone distinctive regulatory evolution, including complete loss of an enhancer that is otherwise highly conserved between chimps and other mammals. Functional tests show that the ancestral enhancer drives expression in hindlimbs but not forelimbs, in locations that have been specifically modified during the human transition to bipedalism. Both gain and loss of regulatory elements can localize BMP changes to specific anatomical locations, providing a flexible regulatory basis for evolving species-specific changes in skeletal form.
骨骼大小和形状的变化是许多脊椎动物的显著特征。在此,我们利用遗传杂交和比较基因组学来识别控制骨骼进化的特定调控DNA改变。棘鱼的甲胄骨大小差异映射到一个与BMP家族成员GDF6重叠的主要效应位点。淡水鱼表达更多的GDF6,部分原因是转座子插入,并且GDF6的转基因过表达模拟了甲胄板大小的进化变化。人类GDF6基因座也经历了独特的调控进化,包括一个增强子的完全丧失,而该增强子在黑猩猩和其他哺乳动物之间高度保守。功能测试表明,祖先增强子在后肢而非前肢驱动表达,在人类向两足行走转变过程中发生了特异性改变的位置。调控元件的获得和丧失都可将BMP变化定位到特定解剖位置,为进化出物种特异性骨骼形态变化提供了灵活的调控基础。