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Pubmed ID :9634230
Publication Date : //

Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence.


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.

Authors : Cole S T , Brosch R , Parkhill J , Garnier T , Churcher C , Harris D , Gordon S V , Eiglmeier K , Gas S , Barry C E , Tekaia F , Badcock K , Basham D , Brown D , Chillingworth T , Connor R , Davies R , Devlin K , Feltwell T , Gentles S , Hamlin N , Holroyd S , Hornsby T , Jagels K , Krogh A , McLean J , Moule S , Murphy L , Oliver K , Osborne J , Quail M A , Rajandream M A , Rogers J , Rutter S , Seeger K , Skelton J , Squares R , Squares S , Sulston J E , Taylor K , Whitehead S , Barrell B G ,

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