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PMID: 2443720 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

S4-alpha mRNA translation regulation complex. II. Secondary structures of the RNA regulatory site in the presence and absence of S4.

Journal of molecular biology ·Vol. 196 ·No. 2 ·1987-07-20 ·Pages 323-32

Deckman IC, Draper DE

Abstract

The secondary structure of the Escherichia coli alpha mRNA leader sequence has been determined using nucleases specific for single- or double-stranded RNA. Three different length alpha RNA fragments were studied at 0 degrees C and 37 degrees C. A very stable eight base-pair helix forms upstream from the ribosome initiation site, defining a 29 base loop. There is evidence for base-pairing between nucleotides within this loop and for a "pseudo-knot" interaction of some loop bases with nucleotides just 3' to the initiation codon, forming a region of complex structure. A weak helix also pairs sequences near the 5' terminus of the alpha mRNA with bases near the Shine-Dalgarno sequence. Affinity constants for the translational repressor S4 binding different length alpha mRNA fragments indicate that most of the S4 recognition features must be contained within the main helix and hairpin regions. Binding of S4 to the alpha mRNA alters the structure of the 29 base hairpin region, and probably melts the weak pairing between the 5' and 3' termini of the leader. The pseudo-knot structure and the conformational changes associated with it provide a link between the structures of the S4 binding site and the ribosome binding site. The alpha mRNA may therefore play an active role in mediating translational repression.

MeSH Terms
Autoradiography Base Sequence Binding Sites Escherichia coli/genetics Models, Molecular Nucleic Acid Conformation Operon Protein Biosynthesis RNA, Bacterial/metabolism RNA, Messenger/metabolism Regulatory Sequences, Nucleic Acid Ribosomal Proteins/metabolism
Chemicals
RNA, Bacterial RNA, Messenger Ribosomal Proteins ribosomal protein S4
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Deckman I C
Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218.
Draper D E
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1987-07-20
Pages
323-32
Language
English
Region
England
NLM ID
2985088R
Subset
IM
Grants
NCI NIH HHS · CA01081 · United States
NIGMS NIH HHS · GM29048 · United States
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