Neisseria gonorrhoeae PilA is an FtsY homolog

被引:11
作者
Arvidson, CG
Powers, T
Walter, P
So, M
机构
[1] Oregon Hlth Sci Univ, Dept Mol Microbiol & Immunol, Portland, OR 97201 USA
[2] Univ Calif San Francisco, Sch Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Sch Med, Dept Biochem & Biophys, San Francisco, CA 94143 USA
关键词
D O I
10.1128/JB.181.3.731-739.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The piLA gene of Neisseria gonorrhoeae was initially identified in a screen for transcriptional regulators of pilE, the expression locus for pilin, the major structural component of gonococcal pill, The predicted protein sequence for PilA has significant homology to two GTPases of the mammalian signal recognition particle (SRP), SRP54 and SR alpha. Homologs of SRP54 and SR alpha were subsequently identified in bacteria (Ffh and FtsY, respectively) and appear to form an SRP-like apparatus in prokaryotes, Of the two proteins, PilA is the most similar to FtsY (37% identical and 67% similar at the amino acid level), Like FtsY, PilA is essential for viability and hydrolyzes GTP. The similarities between PilA and the bacterial FtsY led us to ask whether PilA might function as the gonococcal FtsY, In this work, we show that overproduction of PilA in Escherichia coli leads to an accumulation of pre-P-lactamase, similar to previous observations with other bacterial SRP components. Low-level expression of pilA in an ftsY conditional mutant can complement the ftsY mutation and restore normal growth to this strain under nonpermissive conditions, In addition, purified PilA can replace FtsY in an in vitro translocation assay using purified E. coli SRP components. A PilA mutant that is severely affected in its GTPase activity cannot replace FtsY in vivo or in vitro, However, overexpression of the GTPase mutant leads to the accumulation of pre-beta-lactamase, suggesting that the mutant protein may interact with the SRP apparatus to affect protein maturation. Taken together, these results show that the gonococcal PilA is an FtsY homolog and that the GTPase activity is necessary for its function.
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页码:731 / 739
页数:9
相关论文
共 63 条
  • [21] KUNKEL TA, 1987, METHOD ENZYMOL, V154, P367
  • [22] THE FUNCTIONING OF THE SRP RECEPTOR FTSY IN PROTEIN-TARGETING IN ESCHERICHIA-COLI CORRELATED WITH ITS ABILITY TO BIND AND HYDROLYZE GTP
    KUSTERS, R
    LENTZEN, G
    EPPENS, E
    VANGEEL, A
    VANDERWEIJDEN, CC
    WINTERMEYER, W
    LUIRINK, J
    [J]. FEBS LETTERS, 1995, 372 (2-3) : 253 - 258
  • [23] CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4
    LAEMMLI, UK
    [J]. NATURE, 1970, 227 (5259) : 680 - +
  • [24] A NusG-like protein from Thermotoga maritima binds to DNA and RNA
    Liao, DQ
    Lurz, R
    Dobrinski, B
    Dennis, PP
    [J]. JOURNAL OF BACTERIOLOGY, 1996, 178 (14) : 4089 - 4098
  • [25] SIGNAL-SEQUENCE RECOGNITION BY AN ESCHERICHIA-COLI RIBONUCLEOPROTEIN COMPLEX
    LUIRINK, J
    HIGH, S
    WOOD, H
    GINER, A
    TOLLERVEY, D
    DOBBERSTEIN, B
    [J]. NATURE, 1992, 359 (6397) : 741 - 743
  • [26] AN ALTERNATIVE PROTEIN TARGETING PATHWAY IN ESCHERICHIA-COLI - STUDIES ON THE ROLE OF FTSY
    LUIRINK, J
    TENHAGENJONGMAN, CM
    VANDERWEIJDEN, CC
    OUDEGA, B
    HIGH, S
    DOBBERSTEIN, B
    KUSTERS, R
    [J]. EMBO JOURNAL, 1994, 13 (10) : 2289 - 2296
  • [27] THE FUNCTIONAL-INTEGRATION OF A POLYTOPIC MEMBRANE-PROTEIN OF ESCHERICHIA-COLI IS DEPENDENT ON THE BACTERIAL SIGNAL-RECOGNITION PARTICLE
    MACFARLANE, J
    MULLER, M
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 233 (03): : 766 - 771
  • [28] PHASE VARIATION OF THE OPACITY OUTER-MEMBRANE PROTEIN CONTROLS INVASION BY NEISSERIA-GONORRHOEAE INTO HUMAN EPITHELIAL-CELLS
    MAKINO, S
    VANPUTTEN, JPM
    MEYER, TF
    [J]. EMBO JOURNAL, 1991, 10 (06) : 1307 - 1315
  • [29] Maniatis T., 1982, MOL CLONING A LAB MA
  • [30] PILUS GENES OF NEISSERIA-GONORRHEAE - CHROMOSOMAL ORGANIZATION AND DNA-SEQUENCE
    MEYER, TF
    BILLYARD, E
    HAAS, R
    STORZBACH, S
    SO, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (19): : 6110 - 6114