THE BACTERIOPHAGE-MU GEM GENE - A POSITIVE REGULATOR OF THE C-OPERON REQUIRED FOR NORMAL LEVELS OF LATE TRANSCRIPTION

被引:14
作者
GIUSTI, M
DILALLO, G
GHELARDINI, P
PAOLOZZI, L
机构
[1] CNR,CTR ACIDI NUCL,ROME,ITALY
[2] UNIV ROMA TOR VERGATA,DIPARTIMENTO BIOL,ROME,ITALY
关键词
D O I
10.1016/0042-6822(90)90136-F
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The gem product of bacteriophage Mu modulates synthesis of various host proteins and alters the host chromosome topology. To elucidate the role of the gem gene in Mu development, we analyzed the behavior of several mutants in this gene. The results, obtained with two Mu gem- phages, show that (1) phage growth is significantly delayed and inhibited, (2) early transcription is normal but late transcription is delayed and reduced, (3) DNA replication appears normal, and (4) the Mu C gene, whose product positively regulates Mu late genes, is one of the gem target sites. Transcription of a C promoter-lacZ fusion, carried by the pPH91 plasmid, is stimulated both after infection with Mu gem+ or Mu gem3 and in strains lysogenic for the same phages in the presence of viral immunity. These data suggest that the primary role of the gem product is modulation of gene expression. This control could be carried out by direct interaction with transcription factors or by changing DNA supercoiling. © 1990.
引用
收藏
页码:694 / 700
页数:7
相关论文
共 25 条
[1]   Mitogen-activated protein kinase-defective Candida albicans is avirulent in a novel model of localized murine candidiasis [J].
Guhad, FA ;
Jensen, HE ;
Aalbaek, B ;
Csank, C ;
Mohamed, O ;
Harcus, D ;
Thomas, DY ;
Whiteway, M ;
Hau, J .
FEMS MICROBIOLOGY LETTERS, 1998, 166 (01) :135-139
[2]  
BUU A, 1987, FEMS MICROBIOL LETT, V40, P111
[3]   THE TRANSPOSITION FREQUENCY OF IS1-FLANKED TRANSPOSONS IS A FUNCTION OF THEIR SIZE [J].
CHANDLER, M ;
CLERGET, M ;
GALAS, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 154 (02) :229-243
[4]  
GELLERT M, 1981, ANNU REV BIOCHEM, V54, P171
[5]   SUPPRESSION OF THE THERMOSENSITIVE DNA-LIGASE MUTATIONS IN ESCHERICHIA-COLI-K12 THROUGH MODULATION OF GENE-EXPRESSION INDUCED BY PHAGE-MU [J].
GHELARDINI, P ;
LIEBART, JC ;
PAOLOZZI, L ;
PEDRINI, AM .
MOLECULAR AND GENERAL GENETICS, 1989, 216 (01) :31-36
[6]   THE TOPOISOMERASE ACTIVITY OF T4 AMG39 MUTANT IS RESTORED IN MU-LYSOGENS [J].
GHELARDINI, P ;
PEDRINI, AM ;
PAOLOZZI, L .
FEBS LETTERS, 1982, 137 (01) :49-52
[7]   RESTORATION OF LIGASE ACTIVITY IN ESCHERICHIA-COLI-K12 LIG TS7 STRAIN BY BACTERIOPHAGE-MU AND CLONING OF A DNA FRAGMENT HARBORING THE MU-LIG GENE [J].
GHELARDINI, P ;
PAOLOZZI, L ;
LIEBART, JC .
NUCLEIC ACIDS RESEARCH, 1980, 8 (14) :3157-3173
[8]   ESCHERICHIA-COLI-K-12 GYRB-GENE PRODUCT IS INVOLVED IN THE LETHAL EFFECT OF THE LIGTS2 MUTANT OF BACTERIOPHAGE-MU [J].
GHELARDINI, P ;
LIEBART, JC ;
MARCHELLI, C ;
PEDRINI, AM ;
PAOLOZZI, L .
JOURNAL OF BACTERIOLOGY, 1984, 157 (02) :665-668
[9]  
HARSHEY R, 1987, PHAGE MU
[10]   THE SEQUENCE AND MOM-TRANSACTIVATION FUNCTION OF THE C-GENE OF BACTERIOPHAGE-MU [J].
HEISIG, P ;
KAHMANN, R .
GENE, 1986, 43 (1-2) :59-67