Cited by 85RNA Research and SplicingRNA and protein synthesis mechanismsRNA regulation and disease

Definition of the upstream efficiency element of the simian virus 40 late polyadenylation signal by using in vitro analyses.

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Schek, N, Cooke, C, Alwine, J C·1992·Molecular and Cellular Biology

Abstract

The polyadenylation signal for the late mRNAs of simian virus 40 is known to have sequence elements located both upstream and downstream of the AAUAAA which affect efficiency of utilization of the signal. The upstream efficiency element has been previously characterized by using deletion mutations and transfection analyses. Those studies suggested that the upstream element lies between 13 and 48 nucleotides upstream of the AAUAAA. We have utilized in vitro cleavage and polyadenylation reactions to further define the upstream element. 32P-labeled substrate RNAs were prepared by in vitro transcription from wild-type templates as well as from mutant templates having deletions and linker substitutions in the upstream region. Analysis of these substrates defined the upstream region as sequences between 13 and 51 nucleotides upstream of the AAUAAA, in good agreement with the in vivo results. Within this region, three core elements with the consensus sequence AUUUGURA were identified and were specifically mutated by linker substitution. These core elements were found to contain the active components of the upstream efficiency element. Using substrates with both single and double linker substitution mutations of core elements, we observed that the core elements function in a distance-dependent manner. In mutants containing only one core element, the effect on efficiency increases as the distance between the element and the AAUAAA decreases. In addition, when core elements are present…

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Crossref · 10.1128/mcb.12.12.5386

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  • The SV40 late polyadenylation signal is more efficient than the early polyadenylation signal due to a short upstream element preceding the mRNA cleavage site.

    “Because the late polyadenylation signal sequence acts more efficiently for transgene expression than the early polyadenylation signal sequence due to the presence of a short upstream element preceding the mRNA cleavage site [19,20]”

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Authors
Schek, N., Cooke, C., & Alwine, J. C.
Affiliations
University of Pennsylvania (US)
Venue
Molecular and Cellular Biology
Published
1992-12
Volume
12
Issue
12
Pages
5386-5393
ISSN
  • 0270-7306 (ISSN-L)
  • 1098-5549
OpenAlex
W2103478520
Cited by
85
References
1
Citations by year
2024: 1 · 2023: 4 · 2021: 3 · 2019: 4 · 2018: 1 · 2017: 2 · 2016: 2 · 2014: 1 · 2013: 2 · 2012: 1
FWCI
2.38
Type
journal article
Language
en
Open access
Locations
  • Molecular and Cellular Biology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of General Medical Sciences (GM45773, R01GM045773)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
Keywords
simian virus 40, polyadenylation signal, late mRNA, U1 RNA, cauliflower mosaic virus, sequence conservation
MeSH terms
Base Sequence, HeLa Cells, Humans, Molecular Sequence Data, Mutation, Poly A, Regulatory Sequences, Nucleic Acid, RNA, Messenger, RNA, Viral, Simian virus 40, Transcription, Genetic

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