Department of Biology, Stanford University, Stanford, CA, USA.
Present Address: Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Genome Biol. 2023 Jan 19;24(1):11. doi: 10.1186/s13059-023-02846-8.
Measuring allele-specific expression in interspecies hybrids is a powerful way to detect cis-regulatory changes underlying adaptation. However, it remains difficult to identify genes most likely to explain species-specific traits. Here, we outline a simple strategy that leverages population-scale allele-specific RNA-seq data to identify genes that show constrained cis-regulation within species yet show divergence between species. Applying this strategy to data from human-chimpanzee hybrid cortical organoids, we identify signatures of lineage-specific selection on genes related to saccharide metabolism, neurodegeneration, and primary cilia. We also highlight cis-regulatory divergence in CUX1 and EDNRB that may shape the trajectory of human brain development.
测量种间杂种中的等位基因特异性表达是检测适应相关顺式调控变化的一种强有力的方法。然而,要确定最有可能解释物种特有性状的基因仍然很困难。在这里,我们概述了一种简单的策略,该策略利用基于群体的等位基因特异性 RNA-seq 数据来鉴定在种内受到约束的顺式调控但在种间存在差异的基因。将该策略应用于人-黑猩猩杂交皮质类器官的数据中,我们鉴定出与糖代谢、神经退行性变和初级纤毛相关的基因的谱系特异性选择的特征。我们还强调了 CUX1 和 EDNRB 中的顺式调控分歧,这可能塑造了人类大脑发育的轨迹。