TY - JOUR
T1 - Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions
AU - Girskis, Kelly M.
AU - Stergachis, Andrew B.
AU - DeGennaro, Ellen M.
AU - Doan, Ryan N.
AU - Qian, Xuyu
AU - Johnson, Matthew B.
AU - Wang, Peter P.
AU - Sejourne, Gabrielle M.
AU - Nagy, M. Aurel
AU - Pollina, Elizabeth A.
AU - Sousa, André M.M.
AU - Shin, Taehwan
AU - Kenny, Connor J.
AU - Scotellaro, Julia L.
AU - Debo, Brian M.
AU - Gonzalez, Dilenny M.
AU - Rento, Lariza M.
AU - Yeh, Rebecca C.
AU - Song, Janet H.T.
AU - Beaudin, Marc
AU - Fan, Jean
AU - Kharchenko, Peter V.
AU - Sestan, Nenad
AU - Greenberg, Michael E.
AU - Walsh, Christopher A.
N1 - Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/10/20
Y1 - 2021/10/20
N2 - Human accelerated regions (HARs) are the fastest-evolving regions of the human genome, and many are hypothesized to function as regulatory elements that drive human-specific gene regulatory programs. We interrogate the in vitro enhancer activity and in vivo epigenetic landscape of more than 3,100 HARs during human neurodevelopment, demonstrating that many HARs appear to act as neurodevelopmental enhancers and that sequence divergence at HARs has largely augmented their neuronal enhancer activity. Furthermore, we demonstrate PPP1R17 to be a putative HAR-regulated gene that has undergone remarkable rewiring of its cell type and developmental expression patterns between non-primates and primates and between non-human primates and humans. Finally, we show that PPP1R17 slows neural progenitor cell cycle progression, paralleling the cell cycle length increase seen predominantly in primate and especially human neurodevelopment. Our findings establish HARs as key components in rewiring human-specific neurodevelopmental gene regulatory programs and provide an integrated resource to study enhancer activity of specific HARs.
AB - Human accelerated regions (HARs) are the fastest-evolving regions of the human genome, and many are hypothesized to function as regulatory elements that drive human-specific gene regulatory programs. We interrogate the in vitro enhancer activity and in vivo epigenetic landscape of more than 3,100 HARs during human neurodevelopment, demonstrating that many HARs appear to act as neurodevelopmental enhancers and that sequence divergence at HARs has largely augmented their neuronal enhancer activity. Furthermore, we demonstrate PPP1R17 to be a putative HAR-regulated gene that has undergone remarkable rewiring of its cell type and developmental expression patterns between non-primates and primates and between non-human primates and humans. Finally, we show that PPP1R17 slows neural progenitor cell cycle progression, paralleling the cell cycle length increase seen predominantly in primate and especially human neurodevelopment. Our findings establish HARs as key components in rewiring human-specific neurodevelopmental gene regulatory programs and provide an integrated resource to study enhancer activity of specific HARs.
KW - HARs
KW - cerebral cortex
KW - enhancers
KW - evolution
KW - human accelerated regions
KW - neurodevelopment
UR - http://www.scopus.com/inward/record.url?scp=85117247882&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2021.08.005
DO - 10.1016/j.neuron.2021.08.005
M3 - Article
C2 - 34478631
AN - SCOPUS:85117247882
SN - 0896-6273
VL - 109
SP - 3239-3251.e7
JO - Neuron
JF - Neuron
IS - 20
ER -