Sequences of three promoters for the bacteriophage SP6 RNA polymerase.

Abstract:

:Fragments of SP6 DNA generated by cleavage with Hpa II or Taq I were cloned into the Cla I site of pBR322 and the recombinant plasmids were screened for the presence of SP6 promoter activity by transcription in vitro with purified SP6 RNA polymerase. Three plasmids having promoter activity and small inserts of SP6 DNA were characterized. Hybridization studies showed that all three cloned promoters arose from different regions of the SP6 genome. Comparison of the consensus promoter sequence (5' ATTTAGGtgGACACTATAGAAGgaG 3') with the consensus sequences of promoters recognized by the T3 and T7 RNA polymerases reveals a common core sequence (5'-CACTA-3') extending from -7 to -3, as well as other features that may be important in selective promoter recognition by the phage RNA polymerases.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Brown JE,Klement JF,McAllister WT

doi

10.1093/nar/14.8.3521

subject

Has Abstract

pub_date

1986-04-25 00:00:00

pages

3521-6

issue

8

eissn

0305-1048

issn

1362-4962

journal_volume

14

pub_type

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