Variation in HU composition during growth of Escherichia coli: the heterodimer is required for long term survival

被引:148
作者
Claret, L [1 ]
RouviereYaniv, J [1 ]
机构
[1] INST BIOL PHYSICOCHIM,CNRS,UPR 9073,LAB PHYSIOL BACTERIENNE,F-75005 PARIS,FRANCE
关键词
histone-like protein; heterodimeric protein; growth phase regulation; DNA supercoiling; stationary phase;
D O I
10.1006/jmbi.1997.1310
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 histone-like dimeric HU protein of Escherichia coli is encoded by two closely related genes, hupA and hupB. We show here that expression from the single hupA promoter and from the three hupB promoters varies during growth phase. The weak hupB-P4 promoter is active immediately after dilution. Transcription of the hupA gene is activated early in logarithmic phase. A little later, at mid to late exponential phase, RNA originating at the hupB-P2 promoter is detected. The hupB-P3 promoter is activated last when the cells enter stationary phase. Although the hup mRNAs are unstable, the HU protein is very stable so that the variations in the mRNAs synthesis are reflected in the level of the two HU subunits and in the composition of HU dimers. Cells growing exponentially contain a mixture of homodimeric alpha 2 and heterodimeric alpha beta but no beta 2 is detected. In stationary cells, the predominant form is the heterodimer ap. The presence of the heterodimeric form is required for optimal survival of E. coli after prolonged starvation. The three forms of HU are not equivalent, since beta 2 is incapable of promoting formation of DNA supercoiling like alpha beta and alpha 2 do. The putative roles of each form of HU are discussed. (C) 1997 Academic Press Limited.
引用
收藏
页码:93 / 104
页数:12
相关论文
共 40 条
[11]   THE FIS PROTEIN - ITS NOT JUST FOR DNA INVERSION ANYMORE [J].
FINKEL, SE ;
JOHNSON, RC .
MOLECULAR MICROBIOLOGY, 1992, 6 (22) :3257-3265
[12]   COUPLING OF ESCHERICHIA-COLI HNS MESSENGER-RNA LEVELS TO DNA-SYNTHESIS BY AUTOREGULATION - IMPLICATIONS FOR GROWTH-PHASE CONTROL [J].
FREE, A ;
DORMAN, CJ .
MOLECULAR MICROBIOLOGY, 1995, 18 (01) :101-113
[13]   NICKING-CLOSING ENZYME ASSEMBLES NUCLEOSOME-LIKE STRUCTURES INVITRO [J].
GERMOND, JE ;
ROUVIEREYANIV, J ;
YANIV, M ;
BRUTLAG, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (08) :3779-3783
[14]   SURVIVAL OF HUNGER AND STRESS - THE ROLE OF RPOS IN EARLY STATIONARY PHASE GENE-REGULATION IN ESCHERICHIA-COLI [J].
HENGGEARONIS, R .
CELL, 1993, 72 (02) :165-168
[15]   MULTIPLE DEFECTS IN ESCHERICHIA-COLI MUTANTS LACKING HU PROTEIN [J].
HUISMAN, O ;
FAELEN, M ;
GIRARD, D ;
JAFFE, A ;
TOUSSAINT, A ;
ROUVIEREYANIV, J .
JOURNAL OF BACTERIOLOGY, 1989, 171 (07) :3704-3712
[16]  
JOHNSON RC, 1986, CELL, V46, P531, DOI 10.1016/0092-8674(86)90878-0
[17]   G-INVERSION IN BACTERIOPHAGE-MU-DNA IS STIMULATED BY A SITE WITHIN THE INVERTASE GENE AND A HOST FACTOR [J].
KAHMANN, R ;
RUDT, F ;
KOCH, C ;
MERTENS, G .
CELL, 1985, 41 (03) :771-780
[18]   MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE OF THE HU-1 GENE OF ESCHERICIA-COLI [J].
KANO, Y ;
YOSHINO, S ;
WADA, M ;
YOKOYAMA, K ;
NOBUHARA, M ;
IMAMOTO, F .
MOLECULAR AND GENERAL GENETICS, 1985, 201 (02) :360-362
[19]   CLONING AND SEQUENCING OF THE HU-2 GENE OF ESCHERICHIA-COLI [J].
KANO, Y ;
OSATO, K ;
WADA, M ;
IMAMOTO, F .
MOLECULAR & GENERAL GENETICS, 1987, 209 (02) :408-410
[20]   ESCHERICHIA-COLI HOST FACTOR FOR SITE-SPECIFIC DNA INVERSION - CLONING AND CHARACTERIZATION OF THE FIS GENE [J].
KOCH, C ;
VANDEKERCKHOVE, J ;
KAHMANN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (12) :4237-4241