Cloning of the gene encoding the δ subunit of the human T-cell receptor reveals its physical organization within the α-subunit locus and its involvement in chromosome translocations in T-cell malignancy
Creators
- 1. Wistar Institute of Anatomy and Biology, Philadelphia, PA (USA)
Description
By taking advantage of chromosomal walking techniques, the authors have obtained clones that encompass the T-cell receptor (TCR) δ-chain gene. They analyzed clones spanning the entire Jα region extending 115 kilobases 5' of the TCR α-chain constant region and have shown that the TCR δ-chain gene is located over 80 kilobases 5' of Cα. TCR δ-chain gene is rearranged in the γ/δ-expressing T-cell line Peer and is deleted in α/β-expressing T-cell lines. Sequence analysis of portions of this genomic region demonstrates its identity with previously described cDNA clones corresponding to the Cδ and Jδ segments. Furthermore, they have analyzed a t(8;14)-(q24;q11) chromosome translocation from a T-cell leukemia and have shown that the Jδ segment is rearranged in cells deriving from this tumor and probably directly involved in the translocation. Thus, the newly clones TCR δ chain is implicated in the genesis of chromosome translocations in T-cell malignancies carrying cytogenetic abnormalities of band 14q11
Additional details
Publishing Information
- Journal Title
- Proceedings of the National Academy of Sciences of the United States of America
- Journal Volume
- 85
- Journal Issue
- 11
- Series
- Proc. Natl. Acad. Sci. U.S.A.
- Journal Page Range
- 3933-3937
- ISSN
- 0027-8424
- CODEN
- PNASA
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 21019130
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CHROMOSOMAL ABERRATIONS; DNA SEQUENCING; DNA-CLONING; GENES; GENETIC MAPPING; LEUKEMIA; LEUKEMOGENESIS; MOLECULAR BIOLOGY; MOLECULAR STRUCTURE; NUCLEOTIDES; RECEPTORS; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; CARCINOGENESIS; CLONING; DISEASES; HEMIC DISEASES; MUTATIONS; NEOPLASMS; ORGANIC COMPOUNDS; PATHOGENESIS; STRUCTURAL CHEMICAL ANALYSIS