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Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence
Authors:ST Cole  R Brosch  J Parkhill  T Garnier  C Churcher  D Harris  SV Gordon  K Eiglmeier  S Gas  CE Barry  F Tekaia  K Badcock  D Basham  D Brown  T Chillingworth  R Connor  R Davies  K Devlin  T Feltwell  S Gentles  N Hamlin  S Holroyd  T Hornsby  K Jagels  A Krogh  J McLean  S Moule  L Murphy  K Oliver  J Osborne  MA Quail  MA Rajandream  J Rogers  S Rutter  K Seeger  J Skelton  R Squares  S Squares  JE Sulston  K Taylor  S Whitehead  BG Barrell
Affiliation:Sanger Centre, Wellcome Trust Genome Campus, Hinxton, UK. stcole@pasteur.fr
Abstract:Countless millions of people have died from tuberculosis, a chronic infectious disease caused by the tubercle bacillus. The complete genome sequence of the best-characterized strain of Mycobacterium tuberculosis, H37Rv, has been determined and analysed in order to improve our understanding of the biology of this slow-growing pathogen and to help the conception of new prophylactic and therapeutic interventions. The genome comprises 4,411,529 base pairs, contains around 4,000 genes, and has a very high guanine + cytosine content that is reflected in the biased amino-acid content of the proteins. M. tuberculosis differs radically from other bacteria in that a very large portion of its coding capacity is devoted to the production of enzymes involved in lipogenesis and lipolysis, and to two new families of glycine-rich proteins with a repetitive structure that may represent a source of antigenic variation.
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