1989
DOI: 10.1128/jb.171.6.3440-3448.1989
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Localization and regulation of bacteriophage Mu promoters

Abstract: on Southern blots. Signals were detected from four new promoters in addition to the previously characterized Pe (early), PCM (repressor), and P,om (late) promoters. A major signal upstream of C was first observed at 12 min and intensified thereafter with RNA from cts and C amber but not replication-defective prophages; these characteristics indicate that this signal arises from a middle promoter, which we designate Pm. 40-min RNA, four additional major signals originated in the C-lys, F-G-I, N-P, and com-mom … Show more

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Cited by 37 publications
(55 citation statements)
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“…Transcripts produced during lytic development fall into early, middle, and late classes, which are all transcribed rightward (1,19,26,33; C. F. Marrs, Ph.D. thesis, University of Wisconsin, Madison, 1982). At early times after the induction of a Mu prophage, transcription from P, results in the expression of replication functions (15,33).…”
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confidence: 99%
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“…Transcripts produced during lytic development fall into early, middle, and late classes, which are all transcribed rightward (1,19,26,33; C. F. Marrs, Ph.D. thesis, University of Wisconsin, Madison, 1982). At early times after the induction of a Mu prophage, transcription from P, results in the expression of replication functions (15,33).…”
mentioning
confidence: 99%
“…In addition, Mu development requires the host core RNA polymerase (31). The absence of detectable leader transcripts and the C dependence of ,-galactosidase expression from late promoter-lacZ fusions containing only a few bases of the Mu RNA 5' end make it unlikely that C is an antiterminator (18,26). C binds to Pm.., DNA (20), and its footprint overlaps the late promoter consensus sequence in P,ys and Pmom (2) MATERIALS AND METHODS Media, chemicals, and enzymes.…”
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confidence: 99%
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“…Following entero-bacterial infection, depending on the environment, nutrition and host cell conditions, Mu can form a lysogen or enter a lytic mode of replication for production of progeny phage particles. The lytic cycle is tightly regulated by a transcriptional cascade, which is divided into early, middle, and late phases (Figure 1-9) (Stoddard and Howe, 1989;Marrs and Howe, 1990). Transcription from the early promoter (P e ) is entirely independent of replication and de novo protein synthesis.…”
Section: Bacteriophage Mumentioning
confidence: 99%
“…Early transcription starts from P e and does not require de novo protein synthesis or DNA replication. Middle transcription is dependent upon Mor, an activator protein expressed from the Mu early transcript (Stoddard and Howe, 1989;Mathee and Howe, 1990;Marrs and Howe, 1990). The middle transcript codes for the C protein, the activator of the four late promoters P lys , P I , P P , and P mom .…”
Section: Introductionmentioning
confidence: 99%