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Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line

The gibbon ape leukemia virus (GaLVSF)-infected T cell line, MLA 144, was established from the lymphoma of a gibbon ape. The cell line constitutively expresses IL-2 and its receptor, implying that an autocrine mechanism could be responsible for or contribute toward its growth. To explore the mechani...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1986
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188461/
https://www.ncbi.nlm.nih.gov/pubmed/3021892
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description The gibbon ape leukemia virus (GaLVSF)-infected T cell line, MLA 144, was established from the lymphoma of a gibbon ape. The cell line constitutively expresses IL-2 and its receptor, implying that an autocrine mechanism could be responsible for or contribute toward its growth. To explore the mechanism of constitutive IL-2 expression in MLA 144, we have isolated and characterized cosmid clones representing a normal and a doubly inserted IL-2 allele in this cell line. The map of the normal MLA 144 IL-2 allele closely resembles that of the normal human IL-2 gene. The abnormal allele contains a 3' insertion that is a GaLVSF provirus with two long terminal repeats (LTR) and an internal 3.25 kb deletion. At the 5' end of the abnormal allele is a second insertion that DNA sequencing showed to be an isolated GaLVSF LTR with a transcriptional orientation opposing that of the IL-2 gene. We demonstrate by Northern blotting analysis that the vast majority of transcripts are from the abnormal allele, implying that one or both retroviral insertions are responsible for constitutive expression of the allele.
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spelling pubmed-21884612008-04-17 Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line J Exp Med Articles The gibbon ape leukemia virus (GaLVSF)-infected T cell line, MLA 144, was established from the lymphoma of a gibbon ape. The cell line constitutively expresses IL-2 and its receptor, implying that an autocrine mechanism could be responsible for or contribute toward its growth. To explore the mechanism of constitutive IL-2 expression in MLA 144, we have isolated and characterized cosmid clones representing a normal and a doubly inserted IL-2 allele in this cell line. The map of the normal MLA 144 IL-2 allele closely resembles that of the normal human IL-2 gene. The abnormal allele contains a 3' insertion that is a GaLVSF provirus with two long terminal repeats (LTR) and an internal 3.25 kb deletion. At the 5' end of the abnormal allele is a second insertion that DNA sequencing showed to be an isolated GaLVSF LTR with a transcriptional orientation opposing that of the IL-2 gene. We demonstrate by Northern blotting analysis that the vast majority of transcripts are from the abnormal allele, implying that one or both retroviral insertions are responsible for constitutive expression of the allele. The Rockefeller University Press 1986-11-01 /pmc/articles/PMC2188461/ /pubmed/3021892 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line
title Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line
title_full Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line
title_fullStr Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line
title_full_unstemmed Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line
title_short Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line
title_sort retroviral activation of interleukin 2 gene in a gibbon ape t cell lymphoma line
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188461/
https://www.ncbi.nlm.nih.gov/pubmed/3021892