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Article: Sequences and repertoire of the human T cell receptor α and β chain variable region genes in thymocytes

TitleSequences and repertoire of the human T cell receptor α and β chain variable region genes in thymocytes
Authors
Issue Date1987
Citation
European Journal of Immunology, 1987, v. 17, n. 3, p. 375-383 How to Cite?
AbstractTo compare and contrast the human T cell antigen receptor (TcR) α and β chain messages found in human thymocytes to those previously isolated from human peripheral blood T lymphocytes and other nonthymic sources, 13 TcR α and 13 TcR β cDNA were isolated from a human thymocyte library and the nucleotide sequences were determined. The data indicate that, as was found in the peripheral T lymphocytes, the majority of the TcR α and TcRβ chain thymocyte cDNA were derived from potentially functional messages. Although the thymocyte‐derived TcR cDNA do not contain any unique structural features when compared to TcR cDNA from mature T lymphocytes, 4 new Jα segments, 17 new V‐gene segments (9 Vα; 8 Vβ) and 7 additional V‐gene families (4 Vα and 3 Vβ) and sequences had been identified. The exon CβO, found in many murine thymocyte TcR β messages, was not found in over 75 human β chain messages. Based on these new data, a revised estimate of human TcR Vα, Jα and Vβ repertoires is calculated. The most significant change has been the increase in the estimated number of human TcR Vβ‐gene segments to a total of about 100 distributed among about 18 families. The Vα families are now revised upward to 16, with a total number of Vα segments of 50. The estimate of the Jα segments in humans remains between 50–100. Copyright © 1987 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
Persistent Identifierhttp://hdl.handle.net/10722/292323
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.627
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKimura, Nobuhiro-
dc.contributor.authorToyonaga, Barry-
dc.contributor.authorYoshikai, Yasunobu-
dc.contributor.authorDu, Ran‐Pan ‐P-
dc.contributor.authorMak, Tak W.-
dc.date.accessioned2020-11-17T14:56:13Z-
dc.date.available2020-11-17T14:56:13Z-
dc.date.issued1987-
dc.identifier.citationEuropean Journal of Immunology, 1987, v. 17, n. 3, p. 375-383-
dc.identifier.issn0014-2980-
dc.identifier.urihttp://hdl.handle.net/10722/292323-
dc.description.abstractTo compare and contrast the human T cell antigen receptor (TcR) α and β chain messages found in human thymocytes to those previously isolated from human peripheral blood T lymphocytes and other nonthymic sources, 13 TcR α and 13 TcR β cDNA were isolated from a human thymocyte library and the nucleotide sequences were determined. The data indicate that, as was found in the peripheral T lymphocytes, the majority of the TcR α and TcRβ chain thymocyte cDNA were derived from potentially functional messages. Although the thymocyte‐derived TcR cDNA do not contain any unique structural features when compared to TcR cDNA from mature T lymphocytes, 4 new Jα segments, 17 new V‐gene segments (9 Vα; 8 Vβ) and 7 additional V‐gene families (4 Vα and 3 Vβ) and sequences had been identified. The exon CβO, found in many murine thymocyte TcR β messages, was not found in over 75 human β chain messages. Based on these new data, a revised estimate of human TcR Vα, Jα and Vβ repertoires is calculated. The most significant change has been the increase in the estimated number of human TcR Vβ‐gene segments to a total of about 100 distributed among about 18 families. The Vα families are now revised upward to 16, with a total number of Vα segments of 50. The estimate of the Jα segments in humans remains between 50–100. Copyright © 1987 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim-
dc.languageeng-
dc.relation.ispartofEuropean Journal of Immunology-
dc.titleSequences and repertoire of the human T cell receptor α and β chain variable region genes in thymocytes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/eji.1830170312-
dc.identifier.pmid3494611-
dc.identifier.scopuseid_2-s2.0-0023265665-
dc.identifier.volume17-
dc.identifier.issue3-
dc.identifier.spage375-
dc.identifier.epage383-
dc.identifier.eissn1521-4141-
dc.identifier.isiWOS:A1987H118900011-
dc.identifier.issnl0014-2980-

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