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PMID: 6572947 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

5S rRNA gene transcription factor IIIA alters the helical configuration of DNA.

Reynolds WF, Gottesfeld JM

Abstract

Relaxation of Xenopus 5S plasmid DNA (pX1o8) in the presence of transcription factor (TF) IIIA reduces the linking number of the DNA. Parallel experiments with plasmid pMB9 or cloned hepatitis B viral DNA indicate a degree of non-specific unwinding by TF; however, 60% of the effect observed for pX1o8 is due to specific interaction of TF IIIA with the 5S rRNA gene internal promoter sequence. The extent of unwinding (0.2-0.4 helical turn per TF IIIA binding site) is not consistent with the complete denaturation of the 50-base-pair TF binding site; however, it is consistent with a change in helix rotation, denaturation of 2-4 nucleotides per binding site, or DNA wrapping about a protein core. We show that proteins other than TF IIIA (bovine serum albumin and RNase) have no effect on the linking number of DNA when present during relaxation and that the unwinding activity associated with TF is heat labile. These results suggest that TF IIIA may facilitate transcription by altering the helical configuration of 5S DNA.

MeSH Terms
Animals DNA, Superhelical/genetics DNA-Directed RNA Polymerases/genetics Gene Expression Regulation Genes Nucleic Acid Conformation Operon Plasmids RNA Polymerase III/genetics RNA, Ribosomal/genetics Structure-Activity Relationship Transcription Factors/genetics Transcription, Genetic Xenopus laevis
Chemicals
DNA, Superhelical RNA, Ribosomal Transcription Factors DNA-Directed RNA Polymerases RNA Polymerase III
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Reynolds W F
Gottesfeld J M
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23 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-04-00
Pages
1862-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC393710
Subset
IM
Grants
NIGMS NIH HHS · GM-26453 · United States
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