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Efficiency of utilization of the simian virus 40 late polyadenylation site: effects of upstream sequences.
Open accessAbstract
The late polyadenylation signal of simian virus 40 functions with greater efficiency than the early polyadenylation signal, in turn affecting steady-state mRNA levels. Two chloramphenicol acetyltransferase (CAT) transient expression vectors, pL-EPA and pL-LPA, that differ only in their polyadenylation signals were constructed by using the early and late polyadenylation signals, respectively. In transfections of Cos, CV-1P, or HeLa cells and subsequent Northern blot analysis of CAT-specific RNA, approximately five times more steady-state CAT mRNA was produced in transfections with pL-LPA than with pL-EPA. The basis for this difference was not related to the specific promoter used or to RNA stability. Overall, the difference in steady-state mRNA levels derived from the two plasmids appeared to be attributable to intrinsic properties of the two polyadenylation signals, resulting in distinctly different cleavage and polyadenylation efficiencies. Additionally, we found that the utilization of the late polyadenylation site was dramatically reduced by deletion of sequences between 48 and 29 nucleotides 5' of the AAUAAA hexanucleotide. This reduction of mRNA levels was shown not to be caused by altered stability of mutant precursor RNAs or mRNAs, suggesting that these upstream sequences constitute an element of the late polyadenylation signal and may cause, at least to some extent, the greater efficiency of utilization of the late polyadenylation site.
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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]”
From Optimization of AAV expression cassettes to improve packaging capacity and transgene expression in neurons (2014) · cites this paper as [19]
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Metadata
- Authors
- Carswell, S., & Alwine, J. C.
- Affiliations
- University of Pennsylvania (US)
- ORCID
- Alwine, J C
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 1989-10
- Volume
- 9
- Issue
- 10
- Pages
- 4248-4258
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC362504
- OpenAlex
- W2128163162
- Cited by
- 203
- References
- 0
- Citations by year
- 2025: 1 · 2024: 3 · 2023: 3 · 2022: 2 · 2021: 3 · 2020: 5 · 2019: 3 · 2017: 2 · 2016: 1 · 2015: 3 · 2014: 4 · 2013: 4 · 2012: 4
- FWCI
- 5.03
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular and Cellular Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Cancer Institute (CA 28379-09)
- 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, upstream sequences, mRNA levels, chloramphenicol acetyltransferase reporter
- MeSH terms
- Animals, Haplorhini, Antigens, Viral, Tumor, Cell Line, DNA Mutational Analysis, Humans, Plasmids, Poly A, Promoter Regions, Genetic, Regulatory Sequences, Nucleic Acid, RNA Processing, Post-Transcriptional, RNA, Messenger, RNA, Viral, Simian virus 40, Transcription, Genetic, Transfection, Chloramphenicol O-Acetyltransferase
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