The structure and function of the replication initiator protein (Rep) of pSC101: An analysis based on a novel positive-selection system for the replication-deficient mutants

被引:2
作者
Fueki, T [1 ]
Yamaguchi, K [1 ]
机构
[1] Kanazawa Univ, Inst Gene Res, Kanazawa, Ishikawa 9200934, Japan
关键词
DNA replication; initiator protein; plasmid; positive selection of mutants; pSC101;
D O I
10.1093/oxfordjournals.jbchem.a002999
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plasmid pSC101 encodes a 37.5 kDa Rep (RepA) protein, which binds to three 21-base repeats (DR-1, DR-2, and DR-3) in the replication origin region (ori) of the plasmid to initiate replication. Rep also binds to two palindromic sequences (IR-1 and IR-2) which overlap the rep promoter. The binding of Rep to IR-2 represses the production of Rep itself. It is highly likely that the balance of these functions of Rep plays a major role in controlling the copy number of pSC101. In this study, we developed a positive-selection system for replication-deficient mutants of the initiator protein. This system can be applied to the study of other replication systems by changing ori and rep of pSC101 to the corresponding genes. Thirty-four replication-deficient (Ini(-)) mutants were isolated with this system, and analyzed as to the relation between the structure and function of the Rep protein. Seventeen of these 34 Ini(-) mutants were found to lack auto-repressor activity as well as initiator activity. DNA sequence analysis showed that one-third (from the C-terminus) of Rep is dispensable for the auto-repressor activity, while the initiator activity seems to require the whole protein.
引用
收藏
页码:399 / 405
页数:7
相关论文
共 31 条
[1]   MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE OF THE MUTT-MUTATOR OF ESCHERICHIA-COLI THAT CAUSES A-T TO C-G TRANSVERSION [J].
AKIYAMA, M ;
HORIUCHI, T ;
SEKIGUCHI, M .
MOLECULAR & GENERAL GENETICS, 1987, 206 (01) :9-16
[2]   A 37X103 MOLECULAR-WEIGHT PLASMID-ENCODED PROTEIN IS REQUIRED FOR REPLICATION AND COPY NUMBER CONTROL IN THE PLASMID PSC101 AND ITS TEMPERATURE-SENSITIVE DERIVATIVE PHS1 [J].
ARMSTRONG, KA ;
ACOSTA, R ;
LEDNER, E ;
MACHIDA, Y ;
PANCOTTO, M ;
MCCORMICK, M ;
OHTSUBO, H ;
OHTSUBO, E .
JOURNAL OF MOLECULAR BIOLOGY, 1984, 175 (03) :331-347
[3]   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
[4]   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
[5]   PROTEIN MOTIFS THAT RECOGNIZE STRUCTURAL FEATURES OF DNA [J].
CHURCHILL, MEA ;
TRAVERS, AA .
TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (03) :92-97
[6]   THE NUCLEOTIDE-SEQUENCE OF REPLICATION AND MAINTENANCE FUNCTIONS ENCODED BY PLASMID-PSC101 [J].
CHURCHWARD, G ;
LINDER, P ;
CARO, L .
NUCLEIC ACIDS RESEARCH, 1983, 11 (16) :5645-5659
[7]   Mechanism of recruitment of DnaB helicase to the replication origin of the plasmid pSC101 [J].
Datta, HJ ;
Khatri, GS ;
Bastia, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (01) :73-78
[8]   Open strands adjacent to iterons promote the binding of the replication initiator protein (Rep) of pSC101 to the unit sequence of the iterons in vitro [J].
Fueki, T ;
Sugiura, S ;
Yamaguchi, K .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1996, 1305 (03) :181-188
[9]   THE DNAA PROTEIN COMPLEX WITH THE ESCHERICHIA-COLI CHROMOSOMAL REPLICATION ORIGIN (ORIC) AND OTHER DNA SITES [J].
FULLER, RS ;
FUNNELL, BE ;
KORNBERG, A .
CELL, 1984, 38 (03) :889-900
[10]   Negative control of plasmid pSC101 replication by increased concentrations of both initiator protein and iterons [J].
Furuno, S ;
Watanabe-Murakami, Y ;
Takebe-Suzuki, N ;
Yamaguchi, K .
JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY, 2000, 46 (01) :29-37