Expression of phage P4 integrase is regulated negatively by both Int and Vis

被引:22
作者
Piazzolla, D. [1 ]
Cali, S. [1 ]
Spoldi, E. [1 ]
Forti, F. [1 ]
Sala, C. [1 ]
Magnoni, F. [1 ]
Deho, G. [1 ]
Ghisotti, D. [1 ]
机构
[1] Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy
关键词
D O I
10.1099/vir.0.81875-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Phage P4 int gene encodes the integrase responsible for phage integration into and excision from the Escherichia coli chromosome. Here, the data showing that P4 int expression is regulated in a complex manner at different levels are presented. First of all, the P-int promoter is regulated negatively by both Int and Vis, the P4 excisionase. The N-terminal portion of Int appears to be sufficient for such a negative autoregulation, suggesting that the Int N terminus is implicated in DNA binding. Second, full-length transcripts covering the entire int gene could be detected only upon P4 infection, whereas in P4 lysogens only short 5'-end covering transcripts were detectable. On the other hand, transcripts covering the 5'-end of int were also very abundant upon infection. It thus appears that premature transcription termination and/or mRNA degradation play a role in Int-negative regulation both on the basal prophage transcription and upon infection. Finally, comparison between P-int-lacZ transcriptional and translational fusions suggests that Vis regulates Int expression post-transcriptionally. The findings that Vis is also an RNA-binding protein and that Int may be translated from two different start codons have implications on possible regulation models of Int expression.
引用
收藏
页码:2423 / 2431
页数:9
相关论文
共 50 条
[31]   The P4 promoter of the parvovirus minute virus of mice is developmentally regulated in transgenic P4-LacZ mice [J].
Davis, C ;
Segev-Amzaleg, N ;
Rotem, I ;
Mincberg, M ;
Amir, N ;
Sivan, S ;
Gitelman, I ;
Tal, J .
VIROLOGY, 2003, 306 (02) :268-279
[33]   Progesterone (P4) modulates cytokines expression in temporomandibular joint (TMJ) [J].
Puri, Jyoti ;
Bellinger, Larry ;
Kramer, Phillip .
FASEB JOURNAL, 2009, 23
[34]   Progesterone (P4) modulates cytokines expression in temporomandibular joint (TMJ) [J].
Puri, Jyoti ;
Bellinger, Larry ;
Kramer, Phillip .
FASEB JOURNAL, 2009, 23
[35]   THE CAPSID SIZE-DETERMINING PROTEIN SID FORMS AN EXTERNAL SCAFFOLD ON PHAGE P4 PROCAPSIDS [J].
MARVIK, OJ ;
DOKLAND, T ;
NOKLING, RH ;
JACOBSEN, E ;
LARSEN, T ;
LINDQVIST, BH .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 251 (01) :59-75
[36]   Proximity of both ends of stems P3 and P4 of self-kinasing RNA by ATP [J].
Cho, Bong Rae .
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2007, 28 (04) :689-690
[37]   ORGANIZATION AND EXPRESSION OF THE SATELLITE BACTERIOPHAGE P4 LATE GENE-CLUSTER [J].
DALE, EC ;
CHRISTIE, GE ;
CALENDAR, R .
JOURNAL OF MOLECULAR BIOLOGY, 1986, 192 (04) :793-803
[38]   FUNCTIONAL EXPRESSION OF THE USTILAGO-MAYDIS KILLER TOXIN P4 IN PLANTS [J].
LOGEMANN, S ;
BOLLHOEFER, C ;
SCHELL, J .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, :88-88
[39]   Negatively charged residues interacting with the p4 pocket confer binding specificity to DRB1*0401 [J].
Woulfe, SL ;
Bono, CP ;
Zacheis, ML ;
Kirschmann, DA ;
Baudino, TA ;
Swearingen, C ;
Karr, RW ;
Schwartz, BD .
ARTHRITIS AND RHEUMATISM, 1995, 38 (12) :1744-1753
[40]   Antisense RNA-dependent transcription termination sites that modulate lysogenic development of satellite phage P4 [J].
Briani, F ;
Ghisotti, D ;
Dehò, G .
MOLECULAR MICROBIOLOGY, 2000, 36 (05) :1124-1134