NOVEL ORGANIZATION OF THE SITE-SPECIFIC INTEGRATION AND EXCISION RECOMBINATION FUNCTIONS OF THE STAPHYLOCOCCUS-AUREUS SEROTYPE-F VIRULENCE-CONVERTING PHAGES PHI-13 AND PHI-42

被引:57
作者
CARROLL, D
KEHOE, MA
CAVANAGH, D
COLEMAN, DC
机构
[1] UNIV DUBLIN TRINITY COLL,MOYNE INST,DEPT MICROBIOL,DUBLIN 2,IRELAND
[2] UNIV NEWCASTLE,SCH MED,DEPT MICROBIOL,NEWCASTLE TYNE NE2 4HH,TYNE & WEAR,ENGLAND
[3] UNIV DUBLIN TRINITY COLL,SCH DENT SCI,DEPT ORAL MED & PATHOL,DUBLIN 2,IRELAND
关键词
D O I
10.1111/j.1365-2958.1995.tb02315.x
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
Functions required for site-specific integration and excision of the Staphylococcus aureus serotype F virulence-converting phages phi 13 and phi 42 were localized and characterized. Like other temperate phages, integration of phi 13 and phi 42 sequences was found to require the product of an int gene located close to the phage attP site. Both int genes are almost identical, express proteins possessing characteristic features of the Int (integrase) family of recombinases, but share very little homology with previously described int genes, including those of the serotype B S. aureus phages L54a and phi 11. Nevertheless, all four S. aureus phages share an almost identical short sequence located immediately 5' to these distinct int genes, suggesting a common mechanism of int gene regulation. Upstream from these common sequences, the sequences of phi 13 and phi 42 are quite distinct from each other, and from the corresponding regions of phi 11 and L54a which encode the Xis proteins that are required with Int to mediate site-specific excision of the latter phages. Surprisingly, phi 13 and phi 42 sequences encompassing the attP sites and int genes, but lacking either an adjacent or more distant phage excision protein gene, were sufficient to mediate site-specific excision of integrated phage DNA sequences.
引用
收藏
页码:877 / 893
页数:17
相关论文
共 59 条
  • [1] ABREMSKI K, 1982, J BIOL CHEM, V257, P9658
  • [2] THE INTEGRASE FAMILY OF SITE-SPECIFIC RECOMBINASES - REGIONAL SIMILARITIES AND GLOBAL DIVERSITY
    ARGOS, P
    LANDY, A
    ABREMSKI, K
    EGAN, JB
    HAGGARDLJUNGQUIST, E
    HOESS, RH
    KAHN, ML
    KALIONIS, B
    NARAYANA, SVL
    PIERSON, LS
    STERNBERG, N
    LEONG, JM
    [J]. EMBO JOURNAL, 1986, 5 (02) : 433 - 440
  • [3] LOSS OF ANTIBIOTIC RESISTANCE IN STAPHYLOCOCCUS AUREUS RESULTING FROM GROWTH AT HIGH TEMPERATURE
    ASHESHOV, EH
    [J]. JOURNAL OF GENERAL MICROBIOLOGY, 1966, 42 (03): : 403 - &
  • [4] Ausubel FM, 1987, CURRENT PROTOCOLS MO, V1-5
  • [5] EFFICIENT EXCISION OF PHAGE LAMBDA FROM THE ESCHERICHIA-COLI CHROMOSOME REQUIRES THE FIS PROTEIN
    BALL, CA
    JOHNSON, RC
    [J]. JOURNAL OF BACTERIOLOGY, 1991, 173 (13) : 4027 - 4031
  • [6] STAPHYLOCOCCAL ENTEROTOXIN-A IS ENCODED BY PHAGE
    BETLEY, MJ
    MEKALANOS, JJ
    [J]. SCIENCE, 1985, 229 (4709) : 185 - 187
  • [7] SITE-SPECIFIC DNA CONDENSATION AND PAIRING MEDIATED BY THE INT PROTEIN OF BACTERIOPHAGE-LAMBDA
    BETTER, M
    LU, C
    WILLIAMS, RC
    ECHOLS, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (19): : 5837 - 5841
  • [8] BIRGE EA, 1994, BACTERIAL BACTERIOPH, P361
  • [9] EXCISIVE RECOMBINATION OF THE SLP1 ELEMENT IN STREPTOMYCES-LIVIDANS IS MEDIATED BY INT AND ENHANCED BY XIS
    BRASCH, MA
    COHEN, SN
    [J]. JOURNAL OF BACTERIOLOGY, 1993, 175 (10) : 3075 - 3082
  • [10] BULLOCK WO, 1987, BIOTECHNIQUES, V5, P376