Science-advisor
REGISTER info/FAQ
Login
username
password
     
forgot password?
register here
 
Research articles
  search articles
  reviews guidelines
  reviews
  articles index
My Pages
my alerts
  my messages
  my reviews
  my favorites
 
 
Stat
Members: 3645
Articles: 2'501'711
Articles rated: 2609

20 April 2024
 
  » pubmed » pmid10830953

 Article overview


The DNA sequence of human chromosome 21
M Hattori ; A Fujiyama ; T D Taylor ; H Watanabe ; T Yada ; H S Park ; A Toyoda ; K Ishii ; Y Totoki ; D K Choi ; Y Groner ; E Soeda ; M Ohki ; T Takagi ; Y Sakaki ; S Taudien ; K Blechschmidt ; A Polley ; U Menzel ; J Delabar ; K Kumpf ; R Lehmann ; D Patterson ; K Reichwald ; A Rump ; M Schillhabel ; A Schudy ; W Zimmermann ; A Rosenthal ; J Kudoh ; K Schibuya ; K Kawasaki ; S Asakawa ; A Shintani ; T Sasaki ; K Nagamine ; S Mitsuyama ; S E Antonarakis ; S Minoshima ; N Shimizu ; G Nordsiek ; K Hornischer ; P Brant ; M Scharfe ; O Schon ; A Desario ; J Reichelt ; G Kauer ; H Blocker ; J Ramser ; A Beck ; S Klages ; S Hennig ; L Riesselmann ; E Dag ; T Haaf ; S Wehrmeyer ; K Borzym ; K Gardiner ; D Nizetic ; F Francis ; H Lehrach ; R Reinhardt ; M L Yaspo ; ;
Date 18 May 2000
Journal Nature, 405 (6784), 311-9
AbstractChromosome 21 is the smallest human autosome. An extra copy of chromosome 21 causes Down syndrome, the most frequent genetic cause of significant mental retardation, which affects up to 1 in 700 live births. Several anonymous loci for monogenic disorders and predispositions for common complex disorders have also been mapped to this chromosome, and loss of heterozygosity has been observed in regions associated with solid tumours. Here we report the sequence and gene catalogue of the long arm of chromosome 21. We have sequenced 33,546,361 base pairs (bp) of DNA with very high accuracy, the largest contig being 25,491,867 bp. Only three small clone gaps and seven sequencing gaps remain, comprising about 100 kilobases. Thus, we achieved 99.7% coverage of 21q. We also sequenced 281,116 bp from the short arm. The structural features identified include duplications that are probably involved in chromosomal abnormalities and repeat structures in the telomeric and pericentromeric regions. Analysis of the chromosome revealed 127 known genes, 98 predicted genes and 59 pseudogenes.
Source PubMed, pmid10830953 doi: 10.1038/35012518
Services Forum | Review | Favorites   
 
Visitor rating: did you like this article? no 1   2   3   4   5   yes

No review found.
 Did you like this article?

This article or document is ...
important:
of broad interest:
readable:
new:
correct:
Global appreciation:

  Note: answers to reviews or questions about the article must be posted in the forum section.
Authors are not allowed to review their own article. They can use the forum section.

browser Mozilla/5.0 AppleWebKit/537.36 (KHTML, like Gecko; compatible; ClaudeBot/1.0; +claudebot@anthropic.com)






ScienXe.org
» my Online CV
» Free


News, job offers and information for researchers and scientists:
home  |  contact  |  terms of use  |  sitemap
Copyright © 2005-2024 - Scimetrica