THE PCSA GENE IS IDENTICAL TO DIND IN ESCHERICHIA-COLI

被引:32
作者
OHMORI, H [1 ]
SAITO, M [1 ]
YASUDA, T [1 ]
NAGATA, T [1 ]
FUJII, T [1 ]
WACHI, M [1 ]
NAGAI, K [1 ]
机构
[1] TOKYO INST TECHNOL, DEPT BIOENGN, YOKOHAMA, KANAGAWA 227, JAPAN
关键词
D O I
10.1128/jb.177.1.156-165.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The pcsA68 mutant of Escherichia coli is a cold-sensitive mutant which forms long filaments with a large nucleoid in the central region at 20 degrees C. We here show that (i) the coding region for the pcsA gene is identical with orfY located upstream of pyrE and can be deleted without loss of viability; (ii) pcsA is also identical to dinD, a DNA damage-inducible gene, whose expression is regulated by the LexA-RecA system; (iii) the cold-sensitive phenotype of the pcsA68 mutation is suppressed by triangle recA or lexA1 (Ind(-)) mutation, but not by sulA inactivation; (iv) overproduction of PcsA68 leads to inhibition of cell growth in recA(+) and triangle recA strains at 20 and 37 degrees C, but PcsA(+) does not show such an effect at any temperature; (v) SOS response is induced in the pcsA68 mutant cells at 20 degrees C. We discuss the possible function of the pcsA gene, comparing it with the sulA or the dif-xerCD function, We also describe a new method for gene disruption with positive and negative selection.
引用
收藏
页码:156 / 165
页数:10
相关论文
共 57 条
[1]   LINKAGE MAP OF ESCHERICHIA-COLI K-12, EDITION-8 [J].
BACHMANN, BJ .
MICROBIOLOGICAL REVIEWS, 1990, 54 (02) :130-197
[2]  
BLAKELY G, 1991, NEW BIOL, V3, P789
[3]   2 RELATED RECOMBINASES ARE REQUIRED FOR SITE-SPECIFIC RECOMBINATION AT DIF AND CER IN ESCHERICHIA-COLI K12 [J].
BLAKELY, G ;
MAY, G ;
MCCULLOCH, R ;
ARCISZEWSKA, LK ;
BURKE, M ;
LOVETT, ST ;
SHERRATT, DJ .
CELL, 1993, 75 (02) :351-361
[4]   CONSTRUCTION AND CHARACTERIZATION OF NEW CLONING VEHICLES .2. MULTIPURPOSE CLONING SYSTEM [J].
BOLIVAR, F ;
RODRIGUEZ, RL ;
GREENE, PJ ;
BETLACH, MC ;
HEYNEKER, HL ;
BOYER, HW ;
CROSA, JH ;
FALKOW, S .
GENE, 1977, 2 (02) :95-113
[5]   DNA-SEQUENCE AND ANALYSIS OF 136 KILOBASES OF THE ESCHERICHIA-COLI GENOME - ORGANIZATIONAL SYMMETRY AROUND THE ORIGIN OF REPLICATION [J].
BURLAND, V ;
PLUNKETT, G ;
DANIELS, DL ;
BLATTNER, FR .
GENOMICS, 1993, 16 (03) :551-561
[6]   INVITRO GENE FUSIONS THAT JOIN AN ENZYMATICALLY ACTIVE BETA-GALACTOSIDASE SEGMENT TO AMINO-TERMINAL FRAGMENTS OF EXOGENOUS PROTEINS - ESCHERICHIA-COLI PLASMID VECTORS FOR THE DETECTION AND CLONING OF TRANSLATIONAL INITIATION SIGNALS [J].
CASADABAN, MJ ;
CHOU, J ;
COHEN, SN .
JOURNAL OF BACTERIOLOGY, 1980, 143 (02) :971-980
[7]   ANALYSIS OF GENE-CONTROL SIGNALS BY DNA-FUSION AND CLONING IN ESCHERICHIA-COLI [J].
CASADABAN, MJ ;
COHEN, SN .
JOURNAL OF MOLECULAR BIOLOGY, 1980, 138 (02) :179-207
[8]   CHARACTERIZATION OF THE PROMOTER FOR THE LEXA REGULATED SULA GENE OF ESCHERICHIA-COLI [J].
COLE, ST .
MOLECULAR & GENERAL GENETICS, 1983, 189 (03) :400-404
[9]  
Faelen M, 1987, PHAGE MU, P309
[10]   MUTATIONS IN THE ESCHERICHIA-COLI DNAG GENE SUGGEST COUPLING BETWEEN DNA-REPLICATION AND CHROMOSOME PARTITIONING [J].
GROMPE, M ;
VERSALOVIC, J ;
KOEUTH, T ;
LUPSKI, JR .
JOURNAL OF BACTERIOLOGY, 1991, 173 (03) :1268-1278