Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells

<p>Abstract</p> <p>The HTLV-1 Tax oncoprotein rapidly induces cytogenetic damage which can be measured by a significant increase in the number of micronuclei (MN) in cells. Tax is thought to have both aneuploidogenic and clastogenic effects. To examine the cellular target for Tax w...

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Main Authors: Iwanaga Yoichi, Zamboni Daniela, Luisetto Roberto, Majone Franca, Jeang Kuan-Teh
Format: Article
Language:English
Published: BMC 2005-07-01
Series:Retrovirology
Online Access:http://www.retrovirology.com/content/2/1/45
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spelling doaj-4ac521eee229479fa6ec4a22ff1772a22020-11-25T00:29:20ZengBMCRetrovirology1742-46902005-07-01214510.1186/1742-4690-2-45Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cellsIwanaga YoichiZamboni DanielaLuisetto RobertoMajone FrancaJeang Kuan-Teh<p>Abstract</p> <p>The HTLV-1 Tax oncoprotein rapidly induces cytogenetic damage which can be measured by a significant increase in the number of micronuclei (MN) in cells. Tax is thought to have both aneuploidogenic and clastogenic effects. To examine the cellular target for Tax which might mechanistically explain the clastogenic phenomenon, we tested the ability of Tax to induce MN in rodents cells genetically defective for either the Ku80 protein or the catalytic subunit of DNA protein kinase (DNAPKcs). We found that cells genetically mutated in Ku80 were refractory to Tax's induction of MN while cells knocked-out for DNAPKcs showed increased number of Tax-induced MN. Using a cytogenetic method termed FISHI (Fluorescent In Situ Hybridization and Incorporation) which measures the number of DNA-breaks in cells that contained unprotected 3'-OH ends, we observed that Tax increased the prevalence of unprotected DNA breaks in Ku80-intact cells, but not in Ku80-mutated cells. Taken together, our findings suggest Ku80 as a cellular factor targeted by Tax in engendering clastogenic DNA damage.</p> http://www.retrovirology.com/content/2/1/45
collection DOAJ
language English
format Article
sources DOAJ
author Iwanaga Yoichi
Zamboni Daniela
Luisetto Roberto
Majone Franca
Jeang Kuan-Teh
spellingShingle Iwanaga Yoichi
Zamboni Daniela
Luisetto Roberto
Majone Franca
Jeang Kuan-Teh
Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells
Retrovirology
author_facet Iwanaga Yoichi
Zamboni Daniela
Luisetto Roberto
Majone Franca
Jeang Kuan-Teh
author_sort Iwanaga Yoichi
title Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells
title_short Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells
title_full Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells
title_fullStr Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells
title_full_unstemmed Ku protein as a potential human T-cell leukemia virus type 1 (HTLV-1) Tax target in clastogenic chromosomal instability of mammalian cells
title_sort ku protein as a potential human t-cell leukemia virus type 1 (htlv-1) tax target in clastogenic chromosomal instability of mammalian cells
publisher BMC
series Retrovirology
issn 1742-4690
publishDate 2005-07-01
description <p>Abstract</p> <p>The HTLV-1 Tax oncoprotein rapidly induces cytogenetic damage which can be measured by a significant increase in the number of micronuclei (MN) in cells. Tax is thought to have both aneuploidogenic and clastogenic effects. To examine the cellular target for Tax which might mechanistically explain the clastogenic phenomenon, we tested the ability of Tax to induce MN in rodents cells genetically defective for either the Ku80 protein or the catalytic subunit of DNA protein kinase (DNAPKcs). We found that cells genetically mutated in Ku80 were refractory to Tax's induction of MN while cells knocked-out for DNAPKcs showed increased number of Tax-induced MN. Using a cytogenetic method termed FISHI (Fluorescent In Situ Hybridization and Incorporation) which measures the number of DNA-breaks in cells that contained unprotected 3'-OH ends, we observed that Tax increased the prevalence of unprotected DNA breaks in Ku80-intact cells, but not in Ku80-mutated cells. Taken together, our findings suggest Ku80 as a cellular factor targeted by Tax in engendering clastogenic DNA damage.</p>
url http://www.retrovirology.com/content/2/1/45
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