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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5807
|
pubmed:dateCreated |
1981-6-25
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pubmed:databankReference | |
pubmed:abstractText |
The finding that the diversity (D) and joining (JH) but not the variable (VH) DNA segments of mouse immunoglobulin heavy-chain genes are joined in the DNA of some cloned cytolytic T cells, led to identification and sequencing of three different D DNA segments. Two segments identified on the embryo DNA carry on both the 5' and 3' sides two sets of characteristic sequences separated by a 12-base pair spacer, which have been implicated as recognition signals for a recombinase. The third segment, identified in a form joined with a JHDNA segment in a T cell, carries the recognition signal on the 5' side. These results support the 12/23-base pair model for somatic generation of immunoglobulin V genes, and rule out the possibility that the cytolytic T cells use assembled VH, D and JH sequences to encode their antigen receptors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0028-0836
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
16
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pubmed:volume |
290
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
565-70
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:6783962-Animals,
pubmed-meshheading:6783962-Antibody Diversity,
pubmed-meshheading:6783962-Base Sequence,
pubmed-meshheading:6783962-Binding Sites, Antibody,
pubmed-meshheading:6783962-Chromosome Deletion,
pubmed-meshheading:6783962-Cytotoxicity, Immunologic,
pubmed-meshheading:6783962-Embryo, Mammalian,
pubmed-meshheading:6783962-Immunoglobulin Heavy Chains,
pubmed-meshheading:6783962-Immunoglobulin Variable Region,
pubmed-meshheading:6783962-Mice,
pubmed-meshheading:6783962-Receptors, Antigen, T-Cell,
pubmed-meshheading:6783962-Recombination, Genetic,
pubmed-meshheading:6783962-T-Lymphocytes
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pubmed:year |
1981
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pubmed:articleTitle |
Identification of D segments of immunoglobulin heavy-chain genes and their rearrangement in T lymphocytes.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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