The DNA sequence of human chromosome 22
Ian Dunham,Nobuyoshi Shimizu,Bruce A. Roe,S. Chissoe,Adrienne Hunt,Joanna Collins,Richard Bruskiewich,David Beare,Michele Clamp,Luc J. Smink,R Ainscough,J P Almeida,A K Babbage,C L Bagguley,J Bailey,K F Barlow,K Bates,O. Beasley,Christine P. Bird,S. Blakey,Anne Bridgeman,D. Buck,J. Burgess,J. Burgess,W Burrill,John Burton,C Carder,Nigel P. Carter,Yuan Chen,Graeme T Clark,S. M. Clegg,V. Cobley,Charlotte G. Cole,R. E. Collier,R. Connor,D. Conroy,N Corby,G. J. Coville,Antony V. Cox,J. C. Davis,J. C. Davis,Elisabeth Dawson,Pawandeep Dhami,C. Dockree,S. J. Dodsworth,Richard Durbin,Andrew D. Ellington,Kathryn L. Evans,J. M. Fey,K. Fleming,Lisa French,A. A. Garner,James G. R. Gilbert,Melanie E. Goward,Darren Grafham,Mark Griffiths,C. Hall,C. Hall,Rebekah Hall,G. Hall-Tamlyn,R. W. Heathcott,R. W. Heathcott,Shuk-Mei Ho,S. Holmes,Sarah E. Hunt,Matthew Jones,J K Kershaw,A M Kimberley,A. King,Gavin K. Laird,Cordelia Langford,Margaret A. Leversha,Christine Lloyd,D. M. Lloyd,I. D. Martyn,M Mashreghi-Mohammadi,Lucy Matthews,O. T. McCann,Joseph L. McClay,Stuart McLaren,Amanda McMurray,Sarah Milne,B. J. Mortimore,C. Odell,R. Pavitt,A. V. Pearce,D. Pearson,Benjamin Phillimore,Sam Phillips,Robert W. Plumb,H. Ramsay,Y. Ramsey,Lesley J. Rogers,Mark T. Ross,Carol Scott,Harminder Sehra,C. D. Skuce,S. Smalley,Michelle Smith,Carol Soderlund,L. Spragon,Charles A. Steward,John Sulston,R. M. Swann,M. Vaudin,M. Vaudin,Melanie M. Wall,J. M. Wallis,M. N. Whiteley,M. N. Whiteley,Dave Willey,L. Williams,Scott M. Williams,H. Williamson,H. Williamson,T. E. Wilmer,Laurens G. Wilming,Charmain L. Wright,Tim Hubbard,David R. Bentley,Stephan Beck,Jane Rogers,Shinsei Minoshima,Kazuhiko Kawasaki,Takashi Sasaki,Shuichi Asakawa,Jun Kudoh,Ai Shintani,Kazunori Shibuya,Y. Yoshizaki,Noriaki Aoki,Susumu Mitsuyama,Feng Chen,L. Chu,Judy S. Crabtree,Stéphane Deschamps,A. Do,T. Do,Angela Dorman,F. Fang,Y. Fu,P. Hu,Axin Hua,Steve Kenton,Hongshing Lai,H. I. Lao,Jennifer Lewis,S. Lewis,Shaoping Lin,P. Loh,Eda Malaj,T. Nguyen,Huaqin Pan,S. Phan,S. Qi,Y. Qian,L. Ray,Q. Ren,S. Shaull,D. Sloan,L. Song,Q. Wang,Yuhang Wang,Z. Wang,Jim White,D. Willingham,H. Wu,Ziyun Yao,M. Zhan,Genwei Zhang,Joseph A. Murray,N. Miller,Patrick Minx,Robert S. Fulton,David W. Johnson,G. Bemis,David Bentley,H. Bradshaw,S. Bourne,Matt Cordes,Zijin Du,Lucinda Fulton,D. Goela,Tina Graves,J. Hawkins,K. Hinds,K. Kemp,Phil Latreille,Dan Layman,Philip Ozersky,Tracy Rohlfing,Paul Scheet,C. Walker,A. Wamsley,Patricia Wohldmann,Kymberlie H. Pepin,Joanne O. Nelson,Ian F Korf,Joseph A. Bedell,LaDeana W. Hillier,Elaine R. Mardis,Robert H. Waterston,Richard K. Wilson,Beverly S. Emanuel,Tamim H. Shaikh,Hiroki Kurahashi,Sulagna C. Saitta,M. L. Budarf,Heather E. McDermid,Alexander Johnson,A. C.C. Wong,Bernice E. Morrow,Lisa Edelmann,U. J. Kim,Hiroaki Shizuya,Melvin I. Simon,Jan P. Dumanski,Myriam Peyrard,Darek Kedra,Eyal Seroussi,Ingegerd Fransson,I. Tapia,Carl E.G. Bruder,K. P. O'Brien +223 more
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TLDR
The sequence of the euchromatic part of human chromosome 22 is reported, which consists of 12 contiguous segments spanning 33.4 megabases, contains at least 545 genes and 134 pseudogenes, and provides the first view of the complex chromosomal landscapes that will be found in the rest of the genome.Abstract:
Knowledge of the complete genomic DNA sequence of an organism allows a systematic approach to defining its genetic components. The genomic sequence provides access to the complete structures of all genes, including those without known function, their control elements, and, by inference, the proteins they encode, as well as all other biologically important sequences. Furthermore, the sequence is a rich and permanent source of information for the design of further biological studies of the organism and for the study of evolution through cross-species sequence comparison. The power of this approach has been amply demonstrated by the determination of the sequences of a number of microbial and model organisms. The next step is to obtain the complete sequence of the entire human genome. Here we report the sequence of the euchromatic part of human chromosome 22. The sequence obtained consists of 12 contiguous segments spanning 33.4 megabases, contains at least 545 genes and 134 pseudogenes, and provides the first view of the complex chromosomal landscapes that will be found in the rest of the genome.read more
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Journal ArticleDOI
Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags
Sandro J. de Souza,Anamaria A. Camargo,Marcelo R.S. Briones,Fernando Ferreira Costa,Maria Aparecida Nagai,Sergio Verjovski-Almeida,Marco Antônio Zago,Luis Eduardo Coelho Andrade,Helaine Carrer,Hamza El-Dorry,Enilza Maria Espreáfico,Angelita Habr-Gama,Daniel Giannella-Neto,Gustavo H. Goldman,Arthur Gruber,Christine Hackel,Edna Teruko Kimura,Rui M. B. Maciel,Suely Kazue Nagahashi Marie,Elizabeth A. L. Martins,Marina P. Nobrega,Maria Luísa Paço-Larson,Maria Inês de Moura Campos Pardini,Gonçalo A.G. Pereira,João Bosco Pesquero,Vanderlei Rodrigues,Silvia Regina Rogatto,Ismael Dale Cotrim Guerreiro da Silva,Mari Cleide Sogayar,Maria de Fátima Sonati,Eloiza H. Tajara,Sandro Roberto Valentini,Marcio Luis Acencio,Fernando Lopes Alberto,M. E. J. Amaral,I. Anéas,Mario H. Bengtson,Dirce Maria Carraro,Alex F. Carvalho,Lúcia Helena Carvalho,Janete M. Cerutti,Maria Lucia C. Corrêa,M. C. R. Costa,Cyntia Curcio,Tsieko Gushiken,Paulo L. Ho,Elza Kimura,Luciana C. C. Leite,Gustavo Maia,Paromita Majumder,Mozart Marins,Adriana Yamaguti Matsukuma,Analy Salles de Azevedo Melo,Carlos Alberto Mestriner,E. C. Miracca,Daniela C. Miranda,Ana L. T. O. Nascimento,Francisco G. Nobrega,Elida B. Ojopi,José Rodrigo C. Pandolfi,Luciana Gilbert Pessoa,Paula Rahal,Cláudia Aparecida Rainho,Nancy da Rós,Renata G. de Sá,Magaly M. Sales,Neusa Pereira da Silva,Tereza Cristina Lima Silva,Wilson da Silva,Daniel F. Simão,Josane F. Sousa,Daniella Stecconi,Fernando Tsukumo,Valeria Valente,Heloisa Zalcberg,Ricardo R. Brentani,Luis F.L. Reis,Emmanuel Dias-Neto,Andrew J. G. Simpson +78 more
TL;DR: A set of 250,000 cDNAs that represent partial expressed gene sequences and that are biased toward the central coding regions of the resulting transcripts, termed ORF expressed sequence tags (ORESTES), defined 48 transcribed sequences on chromosome 22 not defined by other sequences.
Journal ArticleDOI
Pseudogenes in metazoa: Origin and features
TL;DR: A survey on the origins, features, abundance and localisation of the different pseudogenes is reported, and some experimental data obtained in the authors' laboratories from the study of a nuclear gene coding for the mitochondrial transcription factor A, a key regulator of mitochondrial biogenesis are reported.
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Mutations of the CHK2 gene are found in some osteosarcomas, but are rare in breast, lung, and ovarian tumors.
Carl W. Miller,Carl W. Miller,Takayuki Ikezoe,Utz Krug,Wolf-K. Hofmann,Sigal Tavor,Vijaya Vegesna,Kunihiro Tsukasaki,Seisho Takeuchi,H. Phillip Koeffler +9 more
TL;DR: Findings of CHK2 gene mutations are consistent with osteosarcoma being a defining tumor of Li‐Fraumeni syndrome and emphasizes the importance of the stress pathway which includes TP53.
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Review of a current role of mass spectrometry for proteome research
TL;DR: This review is intended to give readers a snapshot of current mass spectrometry for proteomics research to cover a brief history of mass Spectrometry proteomic research, peptidomics and proteomics for biomarker search, quantitative proteomics, proteomics with post-translational modification and future perspective of proteomics.
Journal ArticleDOI
A draft annotation and overview of the human genome
Fred A. Wright,William J. Lemon,Wei D. Zhao,Russell Sears,Degen Zhuo,Jian Ping Wang,Hee-Yung Yang,Troy Baer,Don Stredney,Don Stredney,Joe Spitzner,Al Stutz,Al Stutz,Ralf Krahe,Bo Yuan +14 more
TL;DR: A functionally annotated human gene index placed directly on the genome, based on the integration of public transcript, protein, and mapping information, supplemented with computational prediction, is reported here.
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