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Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution

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...

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Autores principales: Gokhman, David, Agoglia, Rachel M., Kinnebrew, Maia, Gordon, Wei, Sun, Danqiong, Bajpai, Vivek K., Naqvi, Sahin, Chen, Coral, Chan, Anthony, Chen, Chider, Petrov, Dmitri A., Ahituv, Nadav, Zhang, Honghao, Mishina, Yuji, Wysocka, Joanna, Rohatgi, Rajat, Fraser, Hunter B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038968/
https://www.ncbi.nlm.nih.gov/pubmed/33731941
http://dx.doi.org/10.1038/s41588-021-00804-3
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author Gokhman, David
Agoglia, Rachel M.
Kinnebrew, Maia
Gordon, Wei
Sun, Danqiong
Bajpai, Vivek K.
Naqvi, Sahin
Chen, Coral
Chan, Anthony
Chen, Chider
Petrov, Dmitri A.
Ahituv, Nadav
Zhang, Honghao
Mishina, Yuji
Wysocka, Joanna
Rohatgi, Rajat
Fraser, Hunter B.
author_facet Gokhman, David
Agoglia, Rachel M.
Kinnebrew, Maia
Gordon, Wei
Sun, Danqiong
Bajpai, Vivek K.
Naqvi, Sahin
Chen, Coral
Chan, Anthony
Chen, Chider
Petrov, Dmitri A.
Ahituv, Nadav
Zhang, Honghao
Mishina, Yuji
Wysocka, Joanna
Rohatgi, Rajat
Fraser, Hunter B.
author_sort Gokhman, David
collection PubMed
description 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 non-genetic confounding factors. We differentiated these cells into cranial neural crest cells (CNCCs), 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 6-fold 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.
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spelling pubmed-80389682021-09-17 Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution Gokhman, David Agoglia, Rachel M. Kinnebrew, Maia Gordon, Wei Sun, Danqiong Bajpai, Vivek K. Naqvi, Sahin Chen, Coral Chan, Anthony Chen, Chider Petrov, Dmitri A. Ahituv, Nadav Zhang, Honghao Mishina, Yuji Wysocka, Joanna Rohatgi, Rajat Fraser, Hunter B. Nat Genet Article 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 non-genetic confounding factors. We differentiated these cells into cranial neural crest cells (CNCCs), 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 6-fold 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. 2021-03-17 2021-04 /pmc/articles/PMC8038968/ /pubmed/33731941 http://dx.doi.org/10.1038/s41588-021-00804-3 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Gokhman, David
Agoglia, Rachel M.
Kinnebrew, Maia
Gordon, Wei
Sun, Danqiong
Bajpai, Vivek K.
Naqvi, Sahin
Chen, Coral
Chan, Anthony
Chen, Chider
Petrov, Dmitri A.
Ahituv, Nadav
Zhang, Honghao
Mishina, Yuji
Wysocka, Joanna
Rohatgi, Rajat
Fraser, Hunter B.
Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
title Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
title_full Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
title_fullStr Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
title_full_unstemmed Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
title_short Human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
title_sort human-chimpanzee fused cells reveal cis-regulatory divergence underlying skeletal evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038968/
https://www.ncbi.nlm.nih.gov/pubmed/33731941
http://dx.doi.org/10.1038/s41588-021-00804-3
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