CONTROL OF BACTERIOPHAGE-P2 GENE-EXPRESSION - ANALYSIS OF TRANSCRIPTION OF THE OGR GENE

被引:10
作者
BIRKELAND, NK
LINDQVIST, BH
CHRISTIE, GE
机构
[1] LAB MICROBIAL GENE TECHNOL,N-1432 AS,NORWAY
[2] UNIV OSLO,DEPT BIOL,DIV MOLEC CELL BIOL,OSLO 3,NORWAY
[3] UNIV OSLO,CTR BIOTECHNOL,OSLO 3,NORWAY
关键词
D O I
10.1128/jb.173.21.6927-6934.1991
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The bacteriophage P2 ogr gene encodes an 8.3-kDa protein that is a positive effector of P2 late gene transcription. The ogr gene is preceded by a promoter sequence (P(ogr)) resembling a normal Escherichia coli promoter and is located just downstream of a late transcription unit. We analyzed the kinetics and regulation of ogr gene transcription by using an ogr-specific antisense RNA probe in an S1 mapping assay. During a normal P2 infection, ogr gene transcription starts from P(ogr) at an intermediate time between the onset of early and late transcription. At late times after infection the ogr gene is contranscribed with the late FETUD operon; the ogr gene product thus positively regulates its own synthesis from the P2 late promoter P(F). Expression of the P2 late genes also requires P2 DNA replication. Complementation experiments and transcriptional analysis show that a nonreplicating P2 phage expresses the ogr gene from P(ogr) but is unable to transcribe the late genes. A P2 ogr-defective phage makes an increased level of ogr mRNA, consistent with autogenous control from P(ogr). Transcription of the ogr gene in the prophage of a P2 heteroimmune lysogen is stimulated after infection with P2, suggesting that P(ogr) is under indirect immunity control and is activated by a yet-unidentified P2 early gene product during infection.
引用
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页码:6927 / 6934
页数:8
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