A rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiae

scientific article

A rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiae is …
instance of (P31):
scholarly articleQ13442814

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P932PMC publication ID1205637
P698PubMed publication ID8243996

P50authorPhilip J FarabaughQ56542827
P2093author name stringY Nakamura
K Kawakami
D J Garfinkel
J D Boeke
J N Strathern
B Faiola
S Pande
D P Moore
P2860cites workNucleotide sequence of a yeast Ty element: evidence for an unusual mechanism of gene expressionQ37686206
Proteolytic processing of Ty3 proteins is required for transpositionQ40043373
Transposition of a Ty3 GAG3-POL3 fusion mutant is limited by availability of capsid proteinQ40067633
Cloning of Yeast Transfer RNA Genes in Escherichia coliQ40761001
Systematic alterations in the anticodon arm make tRNA(Glu)-Suoc a more efficient suppressorQ41364393
Processing of TY1 proteins and formation of Ty1 virus-like particles in Saccharomyces cerevisiaeQ41372450
Symmetry, flexibility and permeability in the structure of yeast retrotransposon virus-like particlesQ41519582
The DNA intermediate in yeast Ty1 element transposition copurifies with virus-like particles: cell-free Ty1 transpositionQ45841053
Ty element transposition: reverse transcriptase and virus-like particlesQ45848654
Ribosomal frameshifting in the yeast retrotransposon Ty: tRNAs induce slippage on a 7 nucleotide minimal siteQ68468601
Ty elements transpose through an RNA intermediateQ70078812
Transformation of intact yeast cells treated with alkali cationsQ24672708
A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiaeQ27860636
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemiaQ27861076
Targeting, disruption, replacement, and allele rescue: integrative DNA transformation in yeastQ28131609
Genetic and molecular analyses of the SUP201 gene: a tRNA(3Arg) nonsense suppressor of yeast cyrl-2Q33523973
Efficient translational frameshifting occurs within a conserved sequence of the overlap between the two genes of a yeast Ty1 transposonQ33648018
Host genes that influence transposition in yeast: the abundance of a rare tRNA regulates Ty1 transposition frequencyQ33866285
Translational suppression in retroviral gene expressionQ36063387
Retrotransposition mechanismsQ36422631
Ribosomal frameshifting efficiency and gag/gag-pol ratio are critical for yeast M1 double-stranded RNA virus propagationQ36698153
Functional organization of the retrotransposon Ty from Saccharomyces cerevisiae: Ty protease is required for transpositionQ36786045
Proteolytic processing of pol-TYB proteins from the yeast retrotransposon Ty1Q36797578
Posttranslational Control of Ty1 Retrotransposition Occurs at the Level of Protein ProcessingQ36817719
Expression of the gag-pol fusion protein of Moloney murine leukemia virus without gag protein does not induce virion formation or proteolytic processingQ36869977
A -1 ribosomal frameshift in a double-stranded RNA virus of yeast forms a gag-pol fusion proteinQ37361923
Single-step selection for Ty1 element retrotranspositionQ37389260
Oligonucleotide-directed double-strand break repair in plasmids of Escherichia coli: a method for site-specific mutagenesisQ37400605
Molecular mechanism of codon recognition by tRNA species with modified uridine in the first position of the anticodonQ37524429
5' untranslated sequences are required for the translational control of a yeast regulatory geneQ37563115
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectSaccharomyces cerevisiaeQ719725
P304page(s)309-320
P577publication date1993-10-01
P1433published inGeneticsQ3100575
P1476titleA rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiae
P478volume135

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cites work (P2860)
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Q37405617tRNA genes rapidly change in evolution to meet novel translational demands.

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