| Literature DB >> 29880660 |
Zev N Kronenberg1, Ian T Fiddes2, David Gordon1,3, Shwetha Murali1,3, Stuart Cantsilieris1, Olivia S Meyerson4, Jason G Underwood1,5, Bradley J Nelson1, Mark J P Chaisson1,6, Max L Dougherty1, Katherine M Munson1, Alex R Hastie7, Mark Diekhans2, Fereydoun Hormozdiari8, Nicola Lorusso9, Kendra Hoekzema1, Ruolan Qiu1, Karen Clark10, Archana Raja1,3, AnneMarie E Welch1, Melanie Sorensen1, Carl Baker1, Robert S Fulton11, Joel Armstrong2, Tina A Graves-Lindsay11, Ahmet M Denli12, Emma R Hoppe1, PingHsun Hsieh1, Christopher M Hill1, Andy Wing Chun Pang7, Joyce Lee7, Ernest T Lam7, Susan K Dutcher11, Fred H Gage12, Wesley C Warren11, Jay Shendure1,3, David Haussler2,13, Valerie A Schneider10, Han Cao7, Mario Ventura9, Richard K Wilson11, Benedict Paten2, Alex Pollen4,14, Evan E Eichler15,3.
Abstract
Genetic studies of human evolution require high-quality contiguous ape genome assemblies that are not guided by the human reference. We coupled long-read sequence assembly and full-length complementary DNA sequencing with a multiplatform scaffolding approach to produce ab initio chimpanzee and orangutan genome assemblies. By comparing these with two long-read de novo human genome assemblies and a gorilla genome assembly, we characterized lineage-specific and shared great ape genetic variation ranging from single- to mega-base pair-sized variants. We identified ~17,000 fixed human-specific structural variants identifying genic and putative regulatory changes that have emerged in humans since divergence from nonhuman apes. Interestingly, these variants are enriched near genes that are down-regulated in human compared to chimpanzee cerebral organoids, particularly in cells analogous to radial glial neural progenitors.Entities:
Mesh:
Year: 2018 PMID: 29880660 PMCID: PMC6178954 DOI: 10.1126/science.aar6343
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728