File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1172/JCI113453
- Scopus: eid_2-s2.0-0023888857
- PMID: 3162460
- WOS: WOS:A1988M842700005
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Comparison of T cell receptor α, β, and γ gene rearrangement and expression in T cell acute lymphoblastic leukemia
Title | Comparison of T cell receptor α, β, and γ gene rearrangement and expression in T cell acute lymphoblastic leukemia |
---|---|
Authors | |
Issue Date | 1988 |
Citation | Journal of Clinical Investigation, 1988, v. 81, n. 4, p. 989-996 How to Cite? |
Abstract | We have analyzed the configuration of the T cell receptor (TCR) α gene using newly developed genomic joining region (Jα) probes, which cover ~80 kb of the Jα region upstream from the constant region in 19 patients with T cell acute lymphoblastic leukemia (T-ALL) and in three CD3- leukemic T cell lines (HSB2, CEM, and MOLT4). In parallel, transcription of the TCR-α, β, and γ genes was examined in 11 of these patients and in the T cell lines. All T-ALL and the three T cell lines exhibited both TCR-γ and β gene rearrangements. 8 of 10 T-ALL and all T cell lines expressed TCR-γ transcripts. All samples tested expressed both TCR-β and CD3-γ transcripts. TCR α transcripts were only observed in CD3+ T-ALL but not in CD3- T-ALL or the CD3- cell lines. Among the CD3+ T-ALL, eight had TCR-α gene rearrangements. In addition, TCR-α gene rearrangements were detected in one CD3- T-ALL and all three T cell lines. These leukemic cells may represent a transient stage between rearrangement and expression and provide an opportunity for analyzing the mechanism regulating the expression of the TCR-α gene. |
Persistent Identifier | http://hdl.handle.net/10722/292337 |
ISSN | 2023 Impact Factor: 13.3 2023 SCImago Journal Rankings: 4.833 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hara, J. | - |
dc.contributor.author | Benedict, S. H. | - |
dc.contributor.author | Champagne, E. | - |
dc.contributor.author | Mak, T. W. | - |
dc.contributor.author | Minden, M. | - |
dc.contributor.author | Gelfand, E. W. | - |
dc.date.accessioned | 2020-11-17T14:56:15Z | - |
dc.date.available | 2020-11-17T14:56:15Z | - |
dc.date.issued | 1988 | - |
dc.identifier.citation | Journal of Clinical Investigation, 1988, v. 81, n. 4, p. 989-996 | - |
dc.identifier.issn | 0021-9738 | - |
dc.identifier.uri | http://hdl.handle.net/10722/292337 | - |
dc.description.abstract | We have analyzed the configuration of the T cell receptor (TCR) α gene using newly developed genomic joining region (Jα) probes, which cover ~80 kb of the Jα region upstream from the constant region in 19 patients with T cell acute lymphoblastic leukemia (T-ALL) and in three CD3- leukemic T cell lines (HSB2, CEM, and MOLT4). In parallel, transcription of the TCR-α, β, and γ genes was examined in 11 of these patients and in the T cell lines. All T-ALL and the three T cell lines exhibited both TCR-γ and β gene rearrangements. 8 of 10 T-ALL and all T cell lines expressed TCR-γ transcripts. All samples tested expressed both TCR-β and CD3-γ transcripts. TCR α transcripts were only observed in CD3+ T-ALL but not in CD3- T-ALL or the CD3- cell lines. Among the CD3+ T-ALL, eight had TCR-α gene rearrangements. In addition, TCR-α gene rearrangements were detected in one CD3- T-ALL and all three T cell lines. These leukemic cells may represent a transient stage between rearrangement and expression and provide an opportunity for analyzing the mechanism regulating the expression of the TCR-α gene. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Clinical Investigation | - |
dc.title | Comparison of T cell receptor α, β, and γ gene rearrangement and expression in T cell acute lymphoblastic leukemia | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1172/JCI113453 | - |
dc.identifier.pmid | 3162460 | - |
dc.identifier.pmcid | PMC329622 | - |
dc.identifier.scopus | eid_2-s2.0-0023888857 | - |
dc.identifier.volume | 81 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | 989 | - |
dc.identifier.epage | 996 | - |
dc.identifier.isi | WOS:A1988M842700005 | - |
dc.identifier.issnl | 0021-9738 | - |