NUCLEOTIDE-SEQUENCE AND PROPERTIES OF THE HRMA LOCUS ASSOCIATED WITH THE PSEUDOMONAS-SYRINGAE PV SYRINGAE 61-HRP GENE-CLUSTER

被引:34
作者
HEU, S [1 ]
HUTCHESON, SW [1 ]
机构
[1] UNIV MARYLAND,DEPT BOT,COLL PK,MD 20742
关键词
GENE REGULATION; HOST RANGE; VIRULENCE;
D O I
10.1094/MPMI-6-553
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
The hrmA locus, isolated from Pseudomonas syringae pv. syringae 61, is essential for phenotypic expression of the P. s. pv. syringae 61 hrp cluster in Escherichia coli strains and enables bacteria carrying the hrp/hrm gene cluster to elicit the hypersensitive response (HR) associated with plant disease resistance. The phenotype of P. s. pv syringae 61 hrmA mutants (pathogenicity(+), delayed HR) was distinct from that of hrp mutants. The locus was localized to a 3.6-kb BamH1-EcoR1 fragment whose nucleotide sequence was determined. A single open reading frame was identified that encodes for a 41,457-Da protein of unknown biochemical function. Production of the deduced protein product was confirmed by using T7 RNA polymerase-directed expression of the locus and N-terminal sequence analysis of the isolated HrmA. The deduced protein product did not exhibit homology with any of the characterized avr genes or the hrpN product of Erwinia amylovora. Transcription was shown to initiate 37 nucleotides upstream of the translational start from an apparent sigma(70) promoter. Two hrp genes were shown to act as positive transcriptional factors for hrmA expression. Expression of hrmA in P. syringae pv. glycinea race 4 did not exhibit the phenotypic properties of an avr gene or HrpN, but suggested that this locus may serve a regulatory function. A homolog to hrmA was present in strains of only three of the 23 P. syringae pathovars tested.
引用
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页码:553 / 564
页数:12
相关论文
共 56 条
[1]  
BEER SV, 1993, BACTERIAL VIRULENCE
[2]   A SIMPLE METHOD TO MONITOR GROWTH OF BACTERIAL-POPULATIONS IN LEAF TISSUE [J].
BERTONI, G ;
MILLS, D .
PHYTOPATHOLOGY, 1987, 77 (06) :832-835
[3]   GENETIC AND STRUCTURAL CHARACTERIZATION OF THE AVIRULENCE GENE AVRBS3 FROM XANTHOMONAS-CAMPESTRIS PV VESICATORIA [J].
BONAS, U ;
STALL, RE ;
STASKAWICZ, B .
MOLECULAR & GENERAL GENETICS, 1989, 218 (01) :127-136
[4]   TRANSPOSITION AND FUSION OF LAC GENES TO SELECTED PROMOTERS IN ESCHERICHIA-COLI USING BACTERIOPHAGE-LAMBDA AND BACTERIOPHAGE-MU [J].
CASADABAN, MJ .
JOURNAL OF MOLECULAR BIOLOGY, 1976, 104 (03) :541-555
[5]  
DERETIC V, 1989, Bio-Technology (New York), V7, P1249
[6]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[7]   MOLECULAR COMMUNICATION IN INTERACTIONS BETWEEN PLANTS AND MICROBIAL PATHOGENS [J].
DIXON, RA ;
LAMB, CJ .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1990, 41 :339-367
[8]   INDUCTION OF ARABIDOPSIS DEFENSE GENES BY VIRULENT AND AVIRULENT PSEUDOMONAS-SYRINGAE STRAINS AND BY A CLONED AVIRULENCE GENE [J].
DONG, XN ;
MINDRINOS, M ;
DAVIS, KR ;
AUSUBEL, FM .
PLANT CELL, 1991, 3 (01) :61-72
[9]  
FELLAY R, 1991, ADV MOL GENETICS PLA, V1, P45
[10]   DETERMINANTS OF PATHOGENICITY IN XANTHOMONAS-CAMPESTRIS PV VESICATORIA ARE RELATED TO PROTEINS INVOLVED IN SECRETION IN BACTERIAL PATHOGENS OF ANIMALS [J].
FENSELAU, S ;
BALBO, I ;
BONAS, U .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1992, 5 (05) :390-396