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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
1995-10-4
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pubmed:abstractText |
The RAG-1 protein plays an essential role in V(D)j recombination, but its exact function has not yet been defined. Here we report that a particular mutation in RAG-1 affects recombination by altering the specificity of target sequence usage. Recombination mediated by wild-type RAG-1 is tolerant of a wide range of coding sequences adjacent to the recombination signal. With the mutant RAG-1, recombination is much more demanding; efficient recombination is only found when particular dinucleotides are adjacent to the signal sequence heptamer. The mutant is also more sensitive than wild-type RAG-1 to certain alterations within the signal sequence. We suggest that the RAG-1 protein may interact physically with the target DNA at the coding-signal sequence border.
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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 |
Sep
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pubmed:issn |
0890-9369
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
9
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pubmed:geneSymbol |
RAG-1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2193-9
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pubmed:dateRevised |
2006-5-1
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pubmed:meshHeading |
pubmed-meshheading:7657170-Base Sequence,
pubmed-meshheading:7657170-Genes, RAG-1,
pubmed-meshheading:7657170-Homeodomain Proteins,
pubmed-meshheading:7657170-Molecular Sequence Data,
pubmed-meshheading:7657170-Mutagenesis, Site-Directed,
pubmed-meshheading:7657170-Mutation,
pubmed-meshheading:7657170-Plasmids,
pubmed-meshheading:7657170-Proteins,
pubmed-meshheading:7657170-Receptors, Antigen, T-Cell,
pubmed-meshheading:7657170-Recombination, Genetic,
pubmed-meshheading:7657170-Sequence Deletion,
pubmed-meshheading:7657170-Transfection
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pubmed:year |
1995
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pubmed:articleTitle |
RAG-1 mutations that affect the target specificity of V(D)j recombination: a possible direct role of RAG-1 in site recognition.
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pubmed:affiliation |
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Bethesda, Maryland 20892, USA.
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pubmed:publicationType |
Journal Article
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