Definition of a novel promoter for the major adenovirus-associated virus mRNA
Abstract
A 660 nucleotide adenovirus-associated virus type 2 (AAV2) DNA fragment which encodes the 5' terminal leader and the entire intervening sequence of the major viral mRNA has been cloned into pBR322, and its primary sequence has been determined. The 5' terminal viral mRNA sequence was deduced by sequencing the reverse-transcriptase cDNA extension product of a 5' end-labeled DNA primer complementary to the RNA 5' terminal region. From combined DNA and RNA sequence analyses (which confirm our previous mapping data) we conclude that the major AAV2 transcript contains a 5' terminal leader sequence about 55 nucleotides in length encoded from a continuous region of DNA (near position 39 on the viral genome) 320 bases from the RNA body. The DNA sequences of the splice junctions are similar to those found for other class II genes. No other nucleotide sequence, indicative of promotion at another (upstream) site, is present at the 5' terminus. The DNA region encoding and flanking the leader sequence displays structural features expected for a class II gene promoter, including the canonical ATATAA sequence 23-25 bases upstream from the presumed initiation site. When the cloned viral DNA fragment is transcribed in vitro by RNA polymerase II in a cell-free system, a transcript is produced with a 5' end that is similar or identical to that found on the in vivo mRNA. Taken together these data strongly suggest that the major polysomal RNA may be generated from a transcription unit with a promo…
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In wild-type AAV, the p5 promoter has been well mapped out and contains a TATA box.
“In the context of wild-type AAV, the p5 promoter has been well mapped out and contains a TATA box,38”
From Adeno-Associated Virus Serotype-Specific Inverted Terminal Repeat Sequence Role in Vector Transgene Expression (2020) · cites this paper as [38]
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Cloning of infectious adeno-associated virus genomes in bacterial plasmids
Laughlin, C. A., Tratschin, J.-D., Coon, H., & Carter, B. J. (1983) · Gene · doi:10.1016/0378-1119(83)90217-2 · Cited by 266 · see citing works
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- Authors
- Green, M. R., & Roeder, R. G.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1980-11
- Volume
- 22
- Issue
- 1
- Pages
- 231-242
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2164382548
- Cited by
- 180
- References
- 1
- Citations by year
- 2025: 1 · 2024: 1 · 2021: 1 · 2020: 2 · 2015: 1 · 2014: 1
- FWCI
- 13.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Cancer Society
- National Cancer Institute
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- splice junctions
- MeSH terms
- Dependovirus, Base Sequence, Cloning, Molecular, DNA, Viral, Genes, Viral, Operon, RNA, Messenger, RNA, Viral, Transcription, Genetic
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