ArticleThe EMBO journal1984
The identification and high level expression of a protein encoded by the yeast Ty element.
Article in The EMBO journal, 1984. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed, 44 citations in OpenAlex.
- The 3-phosphoglycerate kinase gene of the yeast Yarrowia lipolytica de-represses on gluconeogenic substrates.Current genetics · 1996Article
- Symmetry, flexibility and permeability in the structure of yeast retrotransposon virus-like particles.The EMBO journal · 1992Article
- DNA binding of CPF1 is required for optimal centromere function but not for maintaining methionine prototrophy in yeast.Nucleic acids research · 1991Article
- Transcriptional activation by upstream activator sequences requires distinct interactions with downstream elements in the yeast TRP1 promoter.Molecular & general genetics : MGG · 1991Article
- Ty virus-like particles in the Saccharomyces cerevisiae strain NCYC74.Current genetics · 1990Article
- Characterisation of sequences required for RNA initiation from the PGK promoter of Saccharomyces cerevisiae.Nucleic acids research · 1990Article
- Characterization of the transcriptional potency of sub-elements of the UAS of the yeast PGK gene in a PGK mini-promoter.Nucleic acids research · 1989Article
- Complete foldback transposable elements encode a novel protein found in Drosophila melanogaster.The EMBO journal · 1989Article
- Efficient activation of transcription in yeast by the BPV1 E2 protein.Nucleic acids research · 1989Article
- Isolation and characterization of the 3-phosphoglycerate kinase gene (pgk) from the filamentous fungus Trichoderma reesei.Current genetics · 1989Article
- The UAS of the yeast PGK gene is composed of multiple functional elements.Nucleic acids research · 1988Article
- Upstream and downstream transcriptional control signals in the yeast retrotransposon, TY.Nucleic acids research · 1988Article
- The yeast ROAM mutation--identification of the sequences mediating host gene activation and cell-type control in the yeast retrotransposon, Ty.Nucleic acids research · 1987Article
- The production of hybrid Ty:IFN virus-like particles in yeast.Nucleic acids research · 1987Article
- The UAS of the yeast PGK gene contains functionally distinct domains.Nucleic acids research · 1987Article
- A transcriptional activator is located in the coding region of the yeast PGK gene.Nucleic acids research · 1987Article
- Processing of TY1 proteins and formation of Ty1 virus-like particles in Saccharomyces cerevisiae.Molecular & general genetics : MGG · 1987Article
- Multiple control elements in the TRP1 promoter of Saccharomyces cerevisiae.Molecular and cellular biology · 1986Article
- Efficient expression of the Saccharomyces cerevisiae PGK gene depends on an upstream activation sequence but does not require TATA sequences.Molecular and cellular biology · 1986Article
- Expression strategies of the yeast retrotransposon Ty: a short sequence directs ribosomal frameshifting.Nucleic acids research · 1986Article
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Transcription of the yeast Ty element, Ty1 -15, was placed under the control of the efficient PGK promoter on the yeast expression vector, pMA91 . In extracts of yeast transformants containing these constructions a new 52 K basic polypeptide was detected by one- and two-dimensional electrophoresis and was shown, by hybrid arrested translation, to be specifically encoded by the Ty element. The protein coding region was mapped to the first 1.45 kb of the transcribed region of Ty1 -15. These data show for the first time that Ty elements encode proteins and illustrate the general usefulness of high efficiency expression vectors for the detection of rare products.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.