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PMID: 1693642 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Restricted V-(D)-J junctional regions in the T cell response to lambda-repressor. Identification of residues critical for antigen recognition.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 144 ·No. 12 ·1990-06-15 ·Pages 4851-6

Lai MZ, Jang YJ, Chen LK, Gefter ML

Abstract

The T cell response to lambda-repressor is directed to a 15 amino acid peptide (P12-26) of the protein in A/J mice. Previous studies have demonstrated a preferential use of V alpha 2 and V beta 1 amongst the T cell hybridomas specific for P12-26 in the context of I-Ek. By using the polymerase chain reaction, the sequences of a panel of the T cells using V alpha 2 and V beta 1 were determined. A highly conserved alpha-chain V-J junctional sequence was found in six of the eight T cell hybrids. This consensus alpha-chain VJ sequence may be combined with different members of V alpha 2, indicating a more restricted selection on the junctional region than on the V element in these T cells. In contrast, greater diversities were found on the V-D-J region of beta-chains despite the same V beta 1 and J beta 2.1 were used. However, a highly conserved glutamic acid residue was found at the same position of beta-chains where a similar conservation was identified in cytochrome c-specific T cells. The correlation of the TCR sequence with the fine specificities of these T cells suggests that a single amino acid deletion in the V alpha-J alpha region may reduce the P12-26 response and abolish the recognition of an altered peptide [Phe22] P12-26. In addition, three amino acid difference in the V-D-J region of the beta-chain also determine the P12-26 reactivity. Thus the V(D)J junctional regions of both alpha- and beta-chains may be critical for the recognition of the peptide Ag presented by the specific MHC molecule.

MeSH Terms
Amino Acid Sequence Animals Base Sequence DNA-Binding Proteins Dose-Response Relationship, Immunologic Epitopes Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor Gene Rearrangement, beta-Chain T-Cell Antigen Receptor Mice Molecular Sequence Data Polymerase Chain Reaction Receptors, Antigen, T-Cell/genetics,immunology Repressor Proteins/immunology T-Lymphocytes/immunology Transcription Factors/immunology Viral Proteins Viral Regulatory and Accessory Proteins
Chemicals
DNA-Binding Proteins Epitopes Receptors, Antigen, T-Cell Repressor Proteins Transcription Factors Viral Proteins Viral Regulatory and Accessory Proteins phage repressor proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lai M Z
Institute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan, R.O.C.
Jang Y J
Chen L K
Gefter M L
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1990-06-15
Pages
4851-6
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI13357 · United States
NCI NIH HHS · CA28900 · United States
NIGMS NIH HHS · GM37641 · United States
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