Study / S70MQ7I1K2021-01-12
Massively parallel discovery of human-specific substitutions that alter enhancer activity
Severin Uebbing, Jake Gockley, Steven K. Reilly, Acadia A. Kocher, Evan Geller et al.
About this study
Genetic changes that altered the function of gene regulatory elements have been implicated in the evolution of human traits such as the expansion of the cerebral cortex. However, identifying the particular changes that modified regulatory activity during human evolution remain challenging. Here we used massively parallel enhancer assays in neural stem cells to quantify the functional impact of >32,000 human-specific substitutions in >4,300 human accelerated regions (HARs) and human gain enhancers (HGEs), which include enhancers with novel activities in humans. We found that >30% of active HARs and HGEs exhibited differential activity between human and chimpanzee. We isolated the effects of human-specific substitutions from background genetic variation to identify the effects of genetic changes most relevant to human evolution. We found that substitutions interacted in both additive and nonadditive ways to modify enhancer function. Substitutions within HARs, which are highly constrained compared to HGEs, showed smaller effects on enhancer activity, suggesting that the impact of human-specific substitutions is buffered in enhancers with constrained ancestral functions. Our findings yield insight into how human-specific genetic changes altered enhancer function and provide a rich set of candidates for studies of regulatory evolution in humans.
Full author list & citation
Severin Uebbing, Jake Gockley, Steven K. Reilly, Acadia A. Kocher, Evan Geller, Neeru Gandotra, Curt Scharfe, Justin Cotney, James P. Noonan. Massively parallel discovery of human-specific substitutions that alter enhancer activity. 2021-01-12. https://doi.org/10.1073/pnas.2007049118
Experiments 2
E5GUW73MD
Two replicate episomal MPRAs in the same H9-derived human neural stem cell system tested validation fragments and synthetic combinations of human-specific and ancestral alleles on human and chimpanzee background sequences. The library also included negative controls, positive controls, and tile/other control fragments.
E6DEN8WD1
Four replicate episomal MPRAs in H9-derived human neural stem cells tested 137-bp human and chimpanzee orthologous fragments centered on human-specific substitutions in HARs and HGEs. Barcode counts from input plasmid DNA and reporter cDNA were summarized to quantify fragment enhancer activity and human-versus-chimpanzee differences.