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Differential DNA methylation of vocal and facial anatomy genes in modern humans.

David GokhmanMalka Nissim-RafiniaLily Agranat-TamirGenevieve HousmanRaquel García-PérezEsther LizanoOlivia CheronetSwapan MallickMaria A Nieves-ColónHeng LiSongül Alpaslan-RoodenbergMario NovakHongcang GuJason M OsinskiManuel Ferrando-BernalPere GelabertIddi LipendeDeus MjunguIvanela KondovaRonald BontropOttmar KullmerGerhard WeberTal ShaharMona Dvir-GinzbergMarina FaermanEllen E QuillenAlexander MeissnerYonatan LahavLeonid KandelMeir LiebergallMaría E PradaJulio Manuel Vidal EncinasRichard M GronostajskiAnne C StoneBenjamin YakirCarles Lalueza-FoxRon PinhasiDavid ReichTomas Marques-BonetEran MeshorerLiran Carmel
Published in: Nature communications (2020)
Changes in potential regulatory elements are thought to be key drivers of phenotypic divergence. However, identifying changes to regulatory elements that underlie human-specific traits has proven very challenging. Here, we use 63 reconstructed and experimentally measured DNA methylation maps of ancient and present-day humans, as well as of six chimpanzees, to detect differentially methylated regions that likely emerged in modern humans after the split from Neanderthals and Denisovans. We show that genes associated with face and vocal tract anatomy went through particularly extensive methylation changes. Specifically, we identify widespread hypermethylation in a network of face- and voice-associated genes (SOX9, ACAN, COL2A1, NFIX and XYLT1). We propose that these repression patterns appeared after the split from Neanderthals and Denisovans, and that they might have played a key role in shaping the modern human face and vocal tract.
Keyphrases
  • genome wide
  • dna methylation
  • endothelial cells
  • transcription factor
  • gene expression
  • induced pluripotent stem cells
  • stem cells
  • pluripotent stem cells
  • copy number
  • genome wide identification
  • climate change