Department of Biology, Stanford University, Stanford, CA, USA.
Department of Genetics, Stanford University, Stanford, CA, USA.
Nat Genet. 2021 Apr;53(4):467-476. doi: 10.1038/s41588-021-00804-3. Epub 2021 Mar 17.
Gene regulatory divergence is thought to play a central role in determining human-specific traits. However, our ability to link divergent regulation to divergent phenotypes is limited. Here, we utilized human-chimpanzee hybrid induced pluripotent stem cells to study gene expression separating these species. The tetraploid hybrid cells allowed us to separate cis- from trans-regulatory effects, and to control for nongenetic confounding factors. We differentiated these cells into cranial neural crest cells, the primary cell type giving rise to the face. We discovered evidence of lineage-specific selection on the hedgehog signaling pathway, including a human-specific sixfold down-regulation of EVC2 (LIMBIN), a key hedgehog gene. Inducing a similar down-regulation of EVC2 substantially reduced hedgehog signaling output. Mice and humans lacking functional EVC2 show striking phenotypic parallels to human-chimpanzee craniofacial differences, suggesting that the regulatory divergence of hedgehog signaling may have contributed to the unique craniofacial morphology of humans.
基因调控的分歧被认为在决定人类特有的特征方面起着核心作用。然而,我们将分歧的调控与分歧的表型联系起来的能力是有限的。在这里,我们利用人类-黑猩猩杂种诱导多能干细胞来研究将这些物种分开的基因表达。四倍体杂种细胞使我们能够分离顺式和反式调控效应,并控制非遗传混杂因素。我们将这些细胞分化为颅神经嵴细胞,这是产生面部的主要细胞类型。我们发现了 Hedgehog 信号通路中存在谱系特异性选择的证据,包括关键 Hedgehog 基因 EVC2(LIMBIN)的人类特异性六倍下调。诱导 EVC2 的类似下调显著降低了 Hedgehog 信号输出。缺乏功能性 EVC2 的小鼠和人类与人类-黑猩猩颅面差异具有惊人的表型相似性,这表明 Hedgehog 信号的调控分歧可能促成了人类独特的颅面形态。