Identification of dnaX as a high-copy suppressor of the conditional lethal and partition phenotypes of the parE10 allele

被引:19
作者
Levine, C
Marians, KJ
机构
[1] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
[2] Cornell Univ, Grad Sch Med Sci, Mol Biol Grad Program, New York, NY 10021 USA
关键词
D O I
10.1128/JB.180.5.1232-1240.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Termination of DNA replication, complete topological unlinking of the parental template DNA strands, partition of the daughter chromosomes, and cell division follow in an ordered and interdependent sequence during normal bacterial growth, In Escherichia coli, topoisomerase IV (Topo IV), encoded by parE and parC, is responsible for decatenation of the two newly formed chromosomes, In an effort to uncover the pathway of information flow between the macromolecular processes that describe these events, we identified dnaX, encoding the tau and gamma subunits of the DNA polymerase III holoenzyme, as a high-copy suppressor of the temperature-sensitive phenotype of the parE10 allele, We show that suppression derives from overexpression of the gamma, but not the tau, subunit of the holoenzyme and that the partition defect of parE10 cells is nearly completely reverted at the nonpermissive temperature as well, These observations suggest a possible association between Topo IV and the replication machinery.
引用
收藏
页码:1232 / 1240
页数:9
相关论文
共 64 条
  • [1] THE ROLE OF TOPOISOMERASE-IV IN PARTITIONING BACTERIAL REPLICONS AND THE STRUCTURE OF CATENATED INTERMEDIATES IN DNA-REPLICATION
    ADAMS, DE
    SHEKHTMAN, EM
    ZECHIEDRICH, EL
    SCHMID, MB
    COZZARELLI, NR
    [J]. CELL, 1992, 71 (02) : 277 - 288
  • [2] The complete genome sequence of Escherichia coli K-12
    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
    [J]. SCIENCE, 1997, 277 (5331) : 1453 - +
  • [3] THE ESCHERICHIA-COLI DNA POLYMERASE-III HOLOENZYME CONTAINS BOTH PRODUCTS OF THE DNAX GENE, TAU AND GAMMA, BUT ONLY TAU IS ESSENTIAL
    BLINKOVA, A
    HERVAS, C
    STUKENBERG, PT
    ONRUST, R
    ODONNELL, ME
    WALKER, JR
    [J]. JOURNAL OF BACTERIOLOGY, 1993, 175 (18) : 6018 - 6027
  • [4] PROGRAMMED RIBOSOMAL FRAMESHIFTING GENERATES THE ESCHERICHIA-COLI DNA POLYMERASE-III GAMMA SUBUNIT FROM WITHIN THE GAMMA-SUBUNIT READING FRAME
    BLINKOWA, AL
    WALKER, JR
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (07) : 1725 - 1729
  • [5] AMPLIFICATION OF SSB-1 MUTANT SINGLE-STRANDED DNA-BINDING PROTEIN IN ESCHERICHIA-COLI
    CHASE, JW
    MURPHY, JB
    WHITTIER, RF
    LORENSEN, E
    SNINSKY, JJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1983, 164 (02) : 193 - 211
  • [6] NONCHROMOSOMAL ANTIBIOTIC RESISTANCE IN BACTERIA - GENETIC TRANSFORMATION OF ESCHERICHIA-COLI BY R-FACTOR DNA
    COHEN, SN
    CHANG, ACY
    HSU, L
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) : 2110 - &
  • [7] DNAX COMPLEX OF ESCHERICHIA-COLI DNA-POLYMERASE-III HOLOENZYME - CENTRAL ROLE OF TAU IN INITIATION COMPLEX ASSEMBLY AND IN DETERMINING THE FUNCTIONAL ASYMMETRY OF HOLOENZYME
    DALLMANN, HG
    THIMMIG, RL
    MCHENRY, CS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) : 29555 - 29562
  • [8] DNA TOPOISOMERASE-II MUTANT OF SACCHAROMYCES-CEREVISIAE - TOPOISOMERASE-II IS REQUIRED FOR SEGREGATION OF DAUGHTER MOLECULES AT THE TERMINATION OF DNA-REPLICATION
    DINARDO, S
    VOELKEL, K
    STERNGLANZ, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (09): : 2616 - 2620
  • [9] DONOCHIE WD, 1976, NATURE, V264, P328
  • [10] THE GYRB GENE-PRODUCT FUNCTIONS IN BOTH INITIATION AND CHAIN POLYMERIZATION OF ESCHERICHIA-COLI CHROMOSOME-REPLICATION - SUPPRESSION OF THE INITIATION DEFICIENCY IN GYRB-TS MUTANTS BY A CLASS OF RPOB MUTATIONS
    FILUTOWICZ, M
    JONCZYK, P
    [J]. MOLECULAR & GENERAL GENETICS, 1983, 191 (02): : 282 - 287