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PMID: 8548655 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Decreasing the distance between the two conserved sequence elements of histone pre-messenger RNA interferes with 3' processing in vitro.

RNA (New York, N.Y.) ·Vol. 1 ·No. 9 ·1995-11-00 ·Pages 905-14

Cho DC, Scharl EC, Steitz JA

Abstract

Histone mRNA 3' end formation requires the presence of two cis-acting conserved sequence elements: a stem-loop structure upstream from the site of cleavage and a purine-rich region downstream from the site of cleavage called the histone downstream element (HDE). Possible interactions between these two elements and their respective binding factors were investigated by a series of deletions (1-7 nt) in the region between the two. The efficiency of processing decreased as the stem-loop and the HDE were moved closer together. In contrast with the documented ability of the U7 snRNP to direct cleavage at a fixed distance from the HDE in insertion mutants (Scharl & Steitz, 1994), all deletion substrates for which processing was observed were cleaved at or 1-nt upstream from the wild-type site. The reason for the inability of the system to cleave closer to the stem-loop remains unclear, but the removal of stem-loop binding protein(s) (SLBP) did not activate upstream cleavage events. Thus, although the processing machinery measures the distance between the cleavage site and the HDE of mammalian histone pre-mRNAs, there is a barrier limiting how far upstream cleavage can occur. These data allow a reevaluation of the sites of 3' end processing in known histone pre-mRNAs.

MeSH Terms
Animals Base Sequence Binding Sites Conserved Sequence Histones/chemistry,genetics,metabolism Molecular Sequence Data Nuclear Proteins Nucleic Acid Conformation RNA Precursors RNA Processing, Post-Transcriptional RNA, Messenger/chemistry,metabolism RNA-Binding Proteins/genetics,metabolism Ribonucleoproteins, Small Nuclear/metabolism Sequence Deletion Substrate Specificity Transcription, Genetic mRNA Cleavage and Polyadenylation Factors
Chemicals
Histones Nuclear Proteins RNA Precursors RNA, Messenger RNA-Binding Proteins Ribonucleoproteins, Small Nuclear Slbp protein, mouse mRNA Cleavage and Polyadenylation Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Cho D C
Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Boyer Center for Molecular Medicine, Yale University School of Medicine, New Haven, Connecticut 06536-0812, USA.
Scharl E C
Steitz J A
Article Info
Journal
RNA (New York, N.Y.)
Abbr.
RNA
ISSN
1355-8382
Published
1995-11-00
Pages
905-14
Language
English
Region
United States
NLM ID
9509184
PMCID
PMC1369339
Subset
IM
Grants
NIGMS NIH HHS · GM26154 · United States
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