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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-1-2
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pubmed:abstractText |
The product of the td intron open reading frame (ORF) of phage T4 is required for high-frequency transfer of the intervening sequence from intron-plus (In+) to intron-minus (In-) alleles. In vivo studies have demonstrated that the td ORF product targets cleavage of td In- DNA, and that cleavage is correlated with intron inheritance [Quirk et al., Cell 56 (1989) 455-465]. In the present study we show by in vitro synthesis of the td intron ORF product, that the protein possesses endonuclease activity and efficiently cleaves double-stranded DNA at or near the site of intron integration. In addition, we demonstrate that intron insertion is accompanied by co-conversion of the flanking exon sequences. Co-conversion of markers within 50 nt surrounding the site of intron insertion occurred at a high frequency (80-100%), and decreased at greater distance from the intervening sequence. Co-conversion may provide a mechanism for maintaining exon-intron RNA contacts required for accurate splicing of the relocated intron. Cleavage of target DNA by an intron endonuclease and co-conversion of flanking exon sequences are both features associated with mobile introns of eukaryotes, indicating a common mechanism for intron transfer in the eukaryotic and prokaryotic kingdoms.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0378-1119
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
82
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
119-26
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2555262-Base Sequence,
pubmed-meshheading:2555262-DNA,
pubmed-meshheading:2555262-DNA Transposable Elements,
pubmed-meshheading:2555262-Endodeoxyribonucleases,
pubmed-meshheading:2555262-Exons,
pubmed-meshheading:2555262-Gene Conversion,
pubmed-meshheading:2555262-Gene Expression Regulation, Viral,
pubmed-meshheading:2555262-Genes, Viral,
pubmed-meshheading:2555262-Introns,
pubmed-meshheading:2555262-Models, Genetic,
pubmed-meshheading:2555262-RNA Splicing,
pubmed-meshheading:2555262-T-Phages,
pubmed-meshheading:2555262-Viral Structural Proteins
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pubmed:year |
1989
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pubmed:articleTitle |
A site-specific endonuclease and co-conversion of flanking exons associated with the mobile td intron of phage T4.
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pubmed:affiliation |
Wadsworth Center for Laboratory and Research, New York State Department of Health, Albany 12201-0509.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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