rdf:type |
|
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0017428,
umls-concept:C0086418,
umls-concept:C0108779,
umls-concept:C0162326,
umls-concept:C0185117,
umls-concept:C0591833,
umls-concept:C1334043,
umls-concept:C1514468,
umls-concept:C1519595,
umls-concept:C2347858,
umls-concept:C2911684
|
pubmed:issue |
8
|
pubmed:dateCreated |
1992-9-1
|
pubmed:databankReference |
|
pubmed:abstractText |
We have cloned and sequenced human genomic DNA homologous to exons 9 and 10 of the CD3 zeta/eta/theta locus. Although there are open reading frames within the human sequences corresponding to the translated portions of murine exons 9 and 10, we find no evidence of conservation of the encoded polypeptide product. Furthermore, using oligonucleotides derived from these homologous sequences, we are unable to detect human CD3 eta- or CD3 theta-like transcripts by polymerase chain reaction amplification of reverse-transcribed RNA from a variety of human lymphoid tissues. Despite the absence of evidence for conservation of human CD3 eta and CD3 theta, there is a surprising degree of similarity between human and murine nucleotide sequences, not only for exons 9 and 10 (78% and 70%, respectively), but also for the 9/10 intron (71%). A possible mechanism for this conservation is discussed.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD30,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0014-2980
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
22
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2135-40
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:1322304-Animals,
pubmed-meshheading:1322304-Antigens, CD,
pubmed-meshheading:1322304-Antigens, CD3,
pubmed-meshheading:1322304-Antigens, CD30,
pubmed-meshheading:1322304-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:1322304-Antigens, Neoplasm,
pubmed-meshheading:1322304-Base Sequence,
pubmed-meshheading:1322304-Exons,
pubmed-meshheading:1322304-Genome, Human,
pubmed-meshheading:1322304-Humans,
pubmed-meshheading:1322304-Mice,
pubmed-meshheading:1322304-Molecular Sequence Data,
pubmed-meshheading:1322304-Polymerase Chain Reaction,
pubmed-meshheading:1322304-Receptors, Antigen, T-Cell,
pubmed-meshheading:1322304-Sequence Homology, Nucleic Acid,
pubmed-meshheading:1322304-Transcription, Genetic
|
pubmed:year |
1992
|
pubmed:articleTitle |
Human genomic sequences corresponding to murine CD3 eta-related transcripts: lack of conservation or expression of homologous human products.
|
pubmed:affiliation |
Laboratory of Immunobiology, Harvard Medical School, Boston, MA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|