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PMID: 2995922 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The ribosomal RNA promoter of Acanthamoeba castellanii determined by transcription in a cell-free system.

Nucleic acids research ·Vol. 13 ·No. 17 ·1985-09-11 ·Pages 6237-48

Kownin P, Iida CT, Brown-Shimer S, Paule MR

Abstract

The DNA sequences required for faithful initiation of ribosomal RNA transcription were determined. BAL-31 digestion was used to modify the rDNA template by introducing deletions from its 3'- and 5'-ends. The resulting mutant DNAs were tested for template activity individually or in competition with wild type utilizing an in vitro transcription system from Acanthamoeba castellanii. The results identify the sequence extending from -31 to +8 to be absolutely required for transcription. In addition; when the region between -47 and -32 is left intact, transcription is augmented.

MeSH Terms
Amoeba/genetics Animals Base Sequence Cell-Free System Chromosome Deletion DNA Restriction Enzymes Mutation Plasmids Promoter Regions, Genetic RNA, Ribosomal/genetics Templates, Genetic Transcription, Genetic
Chemicals
RNA, Ribosomal DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kownin P
Iida C T
Brown-Shimer S
Paule M R
References (20)
20 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1985-09-11
Pages
6237-48
Language
English
Region
England
NLM ID
0411011
PMCID
PMC321949
Subset
IM
Grants
NIGMS NIH HHS · GM26059 · United States
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