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Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP

BACKGROUND: Among human T cell leukemia virus type 1 (HTLV-1)-infected individuals, there is an association between HTLV-1 tax subgroups (subgroup-A or subgroup-B) and the risk of HAM/TSP in the Japanese population. To investigate the role of HTLV-1 subgroups in viral pathogenesis, we studied the fu...

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Autores principales: Naito, Tadasuke, Yasunaga, Jun-ichirou, Mitobe, Yuichi, Shirai, Kazumasa, Sejima, Hiroe, Ushirogawa, Hiroshi, Tanaka, Yuetsu, Nakamura, Tatsufumi, Hanada, Kousuke, Fujii, Masahiro, Matsuoka, Masao, Saito, Mineki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219256/
https://www.ncbi.nlm.nih.gov/pubmed/30400920
http://dx.doi.org/10.1186/s12977-018-0454-x
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author Naito, Tadasuke
Yasunaga, Jun-ichirou
Mitobe, Yuichi
Shirai, Kazumasa
Sejima, Hiroe
Ushirogawa, Hiroshi
Tanaka, Yuetsu
Nakamura, Tatsufumi
Hanada, Kousuke
Fujii, Masahiro
Matsuoka, Masao
Saito, Mineki
author_facet Naito, Tadasuke
Yasunaga, Jun-ichirou
Mitobe, Yuichi
Shirai, Kazumasa
Sejima, Hiroe
Ushirogawa, Hiroshi
Tanaka, Yuetsu
Nakamura, Tatsufumi
Hanada, Kousuke
Fujii, Masahiro
Matsuoka, Masao
Saito, Mineki
author_sort Naito, Tadasuke
collection PubMed
description BACKGROUND: Among human T cell leukemia virus type 1 (HTLV-1)-infected individuals, there is an association between HTLV-1 tax subgroups (subgroup-A or subgroup-B) and the risk of HAM/TSP in the Japanese population. To investigate the role of HTLV-1 subgroups in viral pathogenesis, we studied the functional difference in the subgroup-specific viral transcriptional regulators Tax and HBZ using microarray analysis, reporter gene assays, and evaluation of viral-host protein–protein interaction. RESULTS: (1) Transcriptional changes in Jurkat Tet-On human T-cells that express each subgroup of Tax or HBZ protein under the control of an inducible promoter revealed different target gene profiles; (2) the number of differentially regulated genes induced by HBZ was 2–3 times higher than that induced by Tax; (3) Tax and HBZ induced the expression of different classes of non-coding RNAs (ncRNAs); (4) the chemokine CXCL10, which has been proposed as a prognostic biomarker for HAM/TSP, was more efficiently induced by subgroup-A Tax (Tax-A) than subgroup-B Tax (Tax-B), in vitro as well as in unmanipulated (ex vivo) PBMCs obtained from HAM/TSP patients; (5) reporter gene assays indicated that although transient Tax expression in an HTLV-1-negative human T-cell line activated the CXCL10 gene promoter through the NF-κB pathway, there was no difference in the ability of each subgroup of Tax to activate the CXCL10 promoter; however, (6) chromatin immunoprecipitation assays showed that the ternary complex containing Tax-A is more efficiently recruited onto the promoter region of CXCL10, which contains two NF-κB binding sites, than that containing Tax-B. CONCLUSIONS: Our results indicate that different HTLV-1 subgroups are characterized by different patterns of host gene expression. Differential expression of pathogenesis-related genes by subgroup-specific Tax or HBZ may be associated with the onset of HAM/TSP. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12977-018-0454-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-62192562018-11-16 Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP Naito, Tadasuke Yasunaga, Jun-ichirou Mitobe, Yuichi Shirai, Kazumasa Sejima, Hiroe Ushirogawa, Hiroshi Tanaka, Yuetsu Nakamura, Tatsufumi Hanada, Kousuke Fujii, Masahiro Matsuoka, Masao Saito, Mineki Retrovirology Research BACKGROUND: Among human T cell leukemia virus type 1 (HTLV-1)-infected individuals, there is an association between HTLV-1 tax subgroups (subgroup-A or subgroup-B) and the risk of HAM/TSP in the Japanese population. To investigate the role of HTLV-1 subgroups in viral pathogenesis, we studied the functional difference in the subgroup-specific viral transcriptional regulators Tax and HBZ using microarray analysis, reporter gene assays, and evaluation of viral-host protein–protein interaction. RESULTS: (1) Transcriptional changes in Jurkat Tet-On human T-cells that express each subgroup of Tax or HBZ protein under the control of an inducible promoter revealed different target gene profiles; (2) the number of differentially regulated genes induced by HBZ was 2–3 times higher than that induced by Tax; (3) Tax and HBZ induced the expression of different classes of non-coding RNAs (ncRNAs); (4) the chemokine CXCL10, which has been proposed as a prognostic biomarker for HAM/TSP, was more efficiently induced by subgroup-A Tax (Tax-A) than subgroup-B Tax (Tax-B), in vitro as well as in unmanipulated (ex vivo) PBMCs obtained from HAM/TSP patients; (5) reporter gene assays indicated that although transient Tax expression in an HTLV-1-negative human T-cell line activated the CXCL10 gene promoter through the NF-κB pathway, there was no difference in the ability of each subgroup of Tax to activate the CXCL10 promoter; however, (6) chromatin immunoprecipitation assays showed that the ternary complex containing Tax-A is more efficiently recruited onto the promoter region of CXCL10, which contains two NF-κB binding sites, than that containing Tax-B. CONCLUSIONS: Our results indicate that different HTLV-1 subgroups are characterized by different patterns of host gene expression. Differential expression of pathogenesis-related genes by subgroup-specific Tax or HBZ may be associated with the onset of HAM/TSP. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12977-018-0454-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-06 /pmc/articles/PMC6219256/ /pubmed/30400920 http://dx.doi.org/10.1186/s12977-018-0454-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Naito, Tadasuke
Yasunaga, Jun-ichirou
Mitobe, Yuichi
Shirai, Kazumasa
Sejima, Hiroe
Ushirogawa, Hiroshi
Tanaka, Yuetsu
Nakamura, Tatsufumi
Hanada, Kousuke
Fujii, Masahiro
Matsuoka, Masao
Saito, Mineki
Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP
title Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP
title_full Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP
title_fullStr Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP
title_full_unstemmed Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP
title_short Distinct gene expression signatures induced by viral transactivators of different HTLV-1 subgroups that confer a different risk of HAM/TSP
title_sort distinct gene expression signatures induced by viral transactivators of different htlv-1 subgroups that confer a different risk of ham/tsp
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219256/
https://www.ncbi.nlm.nih.gov/pubmed/30400920
http://dx.doi.org/10.1186/s12977-018-0454-x
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