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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1995-2-16
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pubmed:databankReference | |
pubmed:abstractText |
Analysis of TCR-beta gene recombination and expression was performed by quantitative PCR amplification technique throughout chicken embryogenesis and development. Our data demonstrated that TCR V beta 1 promoters were turned on by day 10 of embryogenesis, 2 days before detection of TCR-beta gene recombination. The V to D recombination step was first detected by day 11 of embryogenesis whereas DJ and V(D)J rearranged genes were detected 1 day later, on day 12 of embryogenesis. Thus, transcription of unrearranged TCR-beta genes in chickens precedes the expression of V(D)J recombinase activity as in mammals. In contrast, although TCR-beta rearrangement starts with the D to J recombination step in mammals, it can start either by the VD or the DJ step in chickens. Furthermore, reverse transcriptase-PCR amplification of TCR-beta transcripts revealed the presence of two kinds of alternative transcripts. These novel alternatively spliced products appeared in thymocytes from embryonic thymus during colonization periods and were absent in transformed T cell lines. Splicing sites are located in the middle of V beta 1 segments and lead to delta V beta 1-C beta and delta V beta 1-D beta-J beta-C beta transcripts. delta V beta 1-C beta transcripts might lead to synthesis of invariant truncated TCR beta-chains containing the aminoterminal portion of the V beta 1 region followed by the C beta region. Because this type of splicing can be generated by using all known V beta 1 members, these invariant forms could play a role in thymocyte development.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
154
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1256-64
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7822794-Alternative Splicing,
pubmed-meshheading:7822794-Amino Acid Sequence,
pubmed-meshheading:7822794-Animals,
pubmed-meshheading:7822794-Base Sequence,
pubmed-meshheading:7822794-Chick Embryo,
pubmed-meshheading:7822794-Chickens,
pubmed-meshheading:7822794-Cloning, Molecular,
pubmed-meshheading:7822794-Gene Rearrangement, beta-Chain T-Cell Antigen Receptor,
pubmed-meshheading:7822794-Genomic Library,
pubmed-meshheading:7822794-Molecular Sequence Data,
pubmed-meshheading:7822794-Polymerase Chain Reaction,
pubmed-meshheading:7822794-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:7822794-Thymus Gland,
pubmed-meshheading:7822794-Transcription, Genetic
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pubmed:year |
1995
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pubmed:articleTitle |
Ontogeny of TCR V beta 1 expression revealed novel invariant alternative transcripts.
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pubmed:affiliation |
Laboratory of Experimental Biology, URA-CNRS 1135, Pierre and Marie Curie University, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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