The structure and functional analysis of canine T-cell receptor beta region
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
19570582
DOI
10.1016/j.vetimm.2009.06.001
PII: S0165-2427(09)00180-9
Knihovny.cz E-zdroje
- MeSH
- databáze genetické MeSH
- DNA primery genetika MeSH
- druhová specificita MeSH
- genová přestavba - beta řetězec receptoru antigenů T-buněk MeSH
- geny TcR beta * MeSH
- lidé MeSH
- myši MeSH
- psi genetika imunologie MeSH
- sekvence nukleotidů MeSH
- sekvenční homologie nukleových kyselin MeSH
- sestřih RNA MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- psi genetika imunologie MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- DNA primery MeSH
VDJ recombination is a key process in T-cell receptor (TCR) and immunoglobulin (Ig) molecules development. Comparison of ENSEMBL and GenBank database information revealed major differences in dog T-cell receptor beta (TRB) region annotations. ENSEMBL based genomic alignment of dog TRB sequence with human sequence and annotation showed a very similar structure of TRB. However, there is only one cluster of DJC segments in dogs. In dog, 38 V segments are followed by 1 D segment, 6 J segments and 1 C segment. Like humans and mice, dogs have another V segment opposite in orientation downstream of the C segment. V segments anticipated were analyzed using the RT-PCR and capillary electrophoresis. Thirty-one of them were identified in samples of thymus and spleen RNA and thus believed to be subjected to chromosomal rearrangement and RNA splicing. We identified and analyzed probable structure of canine TCR beta region, which is different when compared to sequences published in GenBank or ENSEMBL databases.
Citace poskytuje Crossref.org