| Literature DB >> 15616553 |
Joel Martin1, Cliff Han, Laurie A Gordon, Astrid Terry, Shyam Prabhakar, Xinwei She, Gary Xie, Uffe Hellsten, Yee Man Chan, Michael Altherr, Olivier Couronne, Andrea Aerts, Eva Bajorek, Stacey Black, Heather Blumer, Elbert Branscomb, Nancy C Brown, William J Bruno, Judith M Buckingham, David F Callen, Connie S Campbell, Mary L Campbell, Evelyn W Campbell, Chenier Caoile, Jean F Challacombe, Leslie A Chasteen, Olga Chertkov, Han C Chi, Mari Christensen, Lynn M Clark, Judith D Cohn, Mirian Denys, John C Detter, Mark Dickson, Mira Dimitrijevic-Bussod, Julio Escobar, Joseph J Fawcett, Dave Flowers, Dea Fotopulos, Tijana Glavina, Maria Gomez, Eidelyn Gonzales, David Goodstein, Lynne A Goodwin, Deborah L Grady, Igor Grigoriev, Matthew Groza, Nancy Hammon, Trevor Hawkins, Lauren Haydu, Carl E Hildebrand, Wayne Huang, Sanjay Israni, Jamie Jett, Phillip B Jewett, Kristen Kadner, Heather Kimball, Arthur Kobayashi, Marie-Claude Krawczyk, Tina Leyba, Jonathan L Longmire, Frederick Lopez, Yunian Lou, Steve Lowry, Thom Ludeman, Chitra F Manohar, Graham A Mark, Kimberly L McMurray, Linda J Meincke, Jenna Morgan, Robert K Moyzis, Mark O Mundt, A Christine Munk, Richard D Nandkeshwar, Sam Pitluck, Martin Pollard, Paul Predki, Beverly Parson-Quintana, Lucia Ramirez, Sam Rash, James Retterer, Darryl O Ricke, Donna L Robinson, Alex Rodriguez, Asaf Salamov, Elizabeth H Saunders, Duncan Scott, Timothy Shough, Raymond L Stallings, Malinda Stalvey, Robert D Sutherland, Roxanne Tapia, Judith G Tesmer, Nina Thayer, Linda S Thompson, Hope Tice, David C Torney, Mary Tran-Gyamfi, Ming Tsai, Levy E Ulanovsky, Anna Ustaszewska, Nu Vo, P Scott White, Albert L Williams, Patricia L Wills, Jung-Rung Wu, Kevin Wu, Joan Yang, Pieter Dejong, David Bruce, Norman A Doggett, Larry Deaven, Jeremy Schmutz, Jane Grimwood, Paul Richardson, Daniel S Rokhsar, Evan E Eichler, Paul Gilna, Susan M Lucas, Richard M Myers, Edward M Rubin, Len A Pennacchio.
Abstract
Human chromosome 16 features one of the highest levels of segmentally duplicated sequence among the human autosomes. We report here the 78,884,754 base pairs of finished chromosome 16 sequence, representing over 99.9% of its euchromatin. Manual annotation revealed 880 protein-coding genes confirmed by 1,670 aligned transcripts, 19 transfer RNA genes, 341 pseudogenes and three RNA pseudogenes. These genes include metallothionein, cadherin and iroquois gene families, as well as the disease genes for polycystic kidney disease and acute myelomonocytic leukaemia. Several large-scale structural polymorphisms spanning hundreds of kilobase pairs were identified and result in gene content differences among humans. Whereas the segmental duplications of chromosome 16 are enriched in the relatively gene-poor pericentromere of the p arm, some are involved in recent gene duplication and conversion events that are likely to have had an impact on the evolution of primates and human disease susceptibility.Entities:
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Year: 2004 PMID： 15616553 DOI： 10.1038/nature03187
Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962