Fatty acid biosynthesis in Mycobacterium tuberculosis:: Lateral gene transfer, adaptive evolution, and gene duplication

被引:79
作者
Kinsella, RJ [1 ]
Fitzpatrick, DA [1 ]
Creevey, CJ [1 ]
McInerney, JO [1 ]
机构
[1] Natl Univ Ireland, Dept Biol, Bioinformat & Pharmacogenom Lab, Maynooth, Kildare, Ireland
关键词
D O I
10.1073/pnas.1737230100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mycobacterium tuberculosis is a high GC Gram-positive member of the actinobacteria. The mycobacterial cell wall is composed of a complex assortment of lipids and is the interface between the bacterium and its environment. The biosynthesis of fatty acids plays an essential role in the formation of cell wall components, in particular mycolic acids, which have been targeted by many of the drugs used to treat M. tuberculosis infection. M. tuberculosis has approximate to250 genes involved in fatty acid metabolism, a much higher proportion than in any other organism. in silico methods have been used to compare the genome of M. tuberculosis CDC1551 to a database of 58 complete bacterial genomes. The resulting alignments were scanned for genes specifically involved in fatty acid biosynthetic pathway I. Phylogenetic analysis of these alignments was used to investigate horizontal gene transfer, gene duplication, and adaptive evolution. It was found that of the eight gene families examined, five of the phylogenies reconstructed suggest that the actinobacteria have a closer relationship with the alpha-proteobacteria than expected. This is either due to either an ancient transfer of genes or deep paralogy and subsequent retention of the genes in unrelated lineages. Additionally, adaptive evolution and gene duplication have been an influence in the evolution of the pathway. This study provides a key insight into how M. tuberculosis has developed its unique fatty acid synthetic abilities.
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页码:10320 / 10325
页数:6
相关论文
共 43 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Mycolic acids: Structure, biosynthesis and physiological functions [J].
Barry, CE ;
Lee, RE ;
Mdluli, K ;
Sampson, AE ;
Schroeder, BG ;
Slayden, RA ;
Yuan, Y .
PROGRESS IN LIPID RESEARCH, 1998, 37 (2-3) :143-179
[3]   Comparison of the proteome of Mycobacterium tuberculosis strain H37Rv with clinical isolate CDC 1551 [J].
Betts, JC ;
Dodson, P ;
Quan, S ;
Lewis, AP ;
Thomas, PJ ;
Duncan, K ;
McAdam, RA .
MICROBIOLOGY-SGM, 2000, 146 :3205-3216
[4]   The role of lateral gene transfer in the evolution of isoprenoid biosynthesis pathways [J].
Boucher, Y ;
Doolittle, WF .
MOLECULAR MICROBIOLOGY, 2000, 37 (04) :703-716
[5]   Comparative genomics of the leprosy and tubercle bacilli [J].
Brosch, R ;
Gordon, SV ;
Eiglmeier, K ;
Garnier, T ;
Cole, ST .
RESEARCH IN MICROBIOLOGY, 2000, 151 (02) :135-142
[6]   Opinion - Predicting adaptive evolution [J].
Bush, RM .
NATURE REVIEWS GENETICS, 2001, 2 (05) :387-392
[7]   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-+
[8]   A phylogenomic approach to bacterial phylogeny:: Evidence of a core of genes sharing a common history [J].
Daubin, V ;
Gouy, M ;
Perrière, G .
GENOME RESEARCH, 2002, 12 (07) :1080-1090
[9]   Evolution of an autotransporter:: Domain shuffling and lateral transfer from pathogenic Haemophilus to Neisseria [J].
Davis, J ;
Smith, AL ;
Hughes, WR ;
Golomb, M .
JOURNAL OF BACTERIOLOGY, 2001, 183 (15) :4626-4635
[10]   Mycobacterium tuberculosis in the post-genomic age [J].
Domenech, P ;
Barry, CE ;
Cole, ST .
CURRENT OPINION IN MICROBIOLOGY, 2001, 4 (01) :28-34