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PMID: 3458221 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cloning and sequence analysis of complementary DNA encoding an aberrantly rearranged human T-cell gamma chain.

Dialynas DP, Murre C, Quertermous T, Boss JM, Leiden JM, Seidman JG, Strominger JL

Abstract

Complementary DNA (cDNA) encoding a human T-cell gamma chain has been cloned and sequenced. At the junction of the variable and joining regions, there is an apparent deletion of two nucleotides in the human cDNA sequence relative to the murine gamma-chain cDNA sequence, resulting simultaneously in the generation of an in-frame stop codon and in a translational frameshift. For this reason, the sequence presented here encodes an aberrantly rearranged human T-cell gamma chain. There are several surprising differences between the deduced human and murine gamma-chain amino acid sequences. These include poor homology in the variable region, poor homology in a discrete segment of the constant region precisely bounded by the expected junctions of exon CII, and the presence in the human sequence of five potential sites for N-linked glycosylation.

MeSH Terms
Amino Acid Sequence Base Sequence Cloning, Molecular DNA/genetics Gene Expression Regulation Humans RNA, Messenger/genetics Receptors, Antigen, T-Cell/genetics Recombination, Genetic
Chemicals
RNA, Messenger Receptors, Antigen, T-Cell DNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Dialynas D P
Murre C
Quertermous T
Boss J M
Leiden J M
Seidman J G
Strominger J L
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17 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1986-04-00
Pages
2619-23
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC323350
Subset
IM
Grants
NIAID NIH HHS · AI-18436 · United States
NIAID NIH HHS · AI-19938 · United States
NIAID NIH HHS · F32 AI06860 · United States
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GENBANK
M13231
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