Essential bacterial functions encoded by gene pairs

被引:48
作者
Thomaides, Helena B.
Davison, Ella J.
Burston, Lisa
Johnson, Hazel
Brown, David R.
Hunt, Alison C.
Errington, Jeffery
Czaplewski, Lloyd
机构
[1] Prolysis Ltd, Oxford OX5 1PF, England
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
关键词
D O I
10.1128/JB.01381-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
To address the need for new antibacterials, a number of bacterial genomes have been systematically disrupted to identify essential genes. Such programs have focused on the disruption of single genes and may have missed functions encoded by gene pairs or multiple genes. In this work, we hypothesized that we could predict the identity of pairs of proteins within one organism that have the same function. We identified 135 putative protein pairs in Bacillus subtilis and attempted to disrupt the genes forming these, singly and then in pairs. The single gene disruptions revealed new genes that could not be disrupted individually and other genes required for growth in minimal medium or for sporulation. The pairwise disruptions revealed seven pairs of proteins that are likely to have the same function, as the presence of one protein can compensate for the absence of the other. Six of these pairs are essential for bacterial viability and in four cases show a pattern of species conservation appropriate for potential antibacterial development. This work highlights the importance of combinatorial studies in understanding gene duplication and identifying functional redundancy.
引用
收藏
页码:591 / 602
页数:12
相关论文
共 129 条
[1]   2 HIGHLY SIMILAR MULTIDRUG TRANSPORTERS OF BACILLUS-SUBTILIS WHOSE EXPRESSION IS DIFFERENTIALLY REGULATED [J].
AHMED, M ;
LYASS, L ;
MARKHAM, PN ;
TAYLOR, SS ;
VAZQUEZLASLOP, N ;
NEYFAKH, AA .
JOURNAL OF BACTERIOLOGY, 1995, 177 (14) :3904-3910
[2]   A genome-scale analysis for identification of genes required for growth or survival of Haemophilus influenzae [J].
Akerley, BJ ;
Rubin, EJ ;
Novick, VL ;
Amaya, K ;
Judson, N ;
Mekalanos, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :966-971
[3]   CHARACTERIZATION OF BACILLUS-SUBTILIS RECOMBINATIONAL PATHWAYS [J].
ALONSO, JC ;
LUDER, G ;
TAILOR, RH .
JOURNAL OF BACTERIOLOGY, 1991, 173 (13) :3977-3980
[4]   Genetic analysis of the chromosome segregation protein Spo0J of Bacillus subtilis:: evidence for separate domains involved in DNA binding and interactions with Soj protein [J].
Autret, S ;
Nair, R ;
Errington, J .
MOLECULAR MICROBIOLOGY, 2001, 41 (03) :743-755
[5]   The Mfd protein of Bacillus subtilis 168 is involved in both transcription-coupled DNA repair and DNA recombination [J].
Ayora, S ;
Rojo, F ;
Ogasawara, N ;
Nakai, S ;
Alonso, JC .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 256 (02) :301-318
[6]  
BALASSA G, 1978, ANN INST PASTEUR MIC, VB129, P537
[7]   Mta, a global MerR-type regulator of the Bacillus subtilis multidrug-efflux transporters [J].
Baranova, NN ;
Danchin, A ;
Neyfakh, AA .
MOLECULAR MICROBIOLOGY, 1999, 31 (05) :1549-1559
[8]   Methionine regeneration and aminotransferases in Bacillus subtilis, Bacillus cereus, and Bacillus anthracis [J].
Berger, BJ ;
English, S ;
Chan, G ;
Knodel, MH .
JOURNAL OF BACTERIOLOGY, 2003, 185 (08) :2418-2431
[9]   THE BACILLUS-SUBTILIS 168 ALKALINE PHOSPHATASE-III GENE - IMPACT OF A PHOAIII MUTATION ON TOTAL ALKALINE-PHOSPHATASE SYNTHESIS [J].
BOOKSTEIN, C ;
EDWARDS, CW ;
KAPP, NV ;
HULETT, FM .
JOURNAL OF BACTERIOLOGY, 1990, 172 (07) :3730-3737
[10]   Cloning, sequencing, and characterization of the Bacillus subtilis biotin biosynthetic operon [J].
Bower, S ;
Perkins, JB ;
Yocum, RR ;
Howitt, CL ;
Rahaim, P ;
Pero, J .
JOURNAL OF BACTERIOLOGY, 1996, 178 (14) :4122-4130