Bacterial genome sequencing and drug discovery

被引:17
作者
Allsop, AE [1 ]
机构
[1] Zeneca Pharmaceut, Canc & Infect Res Dept, Macclesfield SK10 4TG, Cheshire, England
关键词
D O I
10.1016/S0958-1669(98)80143-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The availability of bacterial genome sequence information has opened up many new strategies for antibacterial drug hunting. There are obvious benefits for the identification and evaluation of new drug targets, but genomic-based technology is also beginning to provide new tools for the downstream, preclinical, optimisation of compounds. The greatest benefit from these new approaches lies in the ability to examine the entire genome (or several genomes) simultaneously and in total. In this way, one potential target can be evaluated against another, and either the total effects of functional impairment can be established or the effects of a compound can be compared across species.
引用
收藏
页码:637 / 642
页数:6
相关论文
共 56 条
[1]   Year of the genome [J].
Ash, C .
TRENDS IN MICROBIOLOGY, 1997, 5 (04) :135-139
[2]  
*ASM, 1995, REP ASM TASK FORC AN
[3]   Exploiting the complete yeast genome sequence [J].
Bassett, DE ;
Basrai, MA ;
Connelly, C ;
Hyland, KM ;
Kitagawa, K ;
Mayer, ML ;
Morrow, DM ;
Page, AM ;
Resto, VA ;
Skibbens, RV ;
Hieter, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (06) :763-766
[4]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[5]   THE IMPORTANCE OF GENOME ANALYSIS TO THE DRUG DISCOVERY PROCESS [J].
BROWNE, MJ ;
GLOGER, IS ;
HODGSON, JE ;
ROBINSON, JH .
MOLECULAR MEDICINE TODAY, 1995, 1 (08) :373-377
[6]   Use of recombinase gene fusions to identify Vibrio cholerae genes induced during infection [J].
Camilli, A ;
Mekalanos, JJ .
MOLECULAR MICROBIOLOGY, 1995, 18 (04) :671-683
[7]   New approaches to the control of infections caused by antibiotic-resistant bacteria - An industry perspective [J].
Chopra, I ;
Hodgson, J ;
Metcalf, B ;
Poste, G .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (05) :401-403
[8]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[9]   INACTIVATION OF ANTIBIOTICS AND THE DISSEMINATION OF RESISTANCE GENES [J].
DAVIES, J .
SCIENCE, 1994, 264 (5157) :375-382
[10]   Bacterial transcript imaging by hybridization of total RNA to oligonucleotide arrays [J].
de Saizieu, A ;
Certa, U ;
Warrington, J ;
Gray, C ;
Keck, W ;
Mous, J .
NATURE BIOTECHNOLOGY, 1998, 16 (01) :45-48