Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs

Endogenous hot spots of DNA double-strand breaks (DSBs) are tightly linked with transcription patterns and cancer. There are nine hot spots of DSBs (denoted Pleiades) in human rDNA units that are located exclusively inside the intergenic spacer (IGS). Profiles of Pleiades coincide with the profiles...

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Main Authors: Nickolai A. Tchurikov, Leonid A. Uroshlev, Elena S. Klushevskaya, Ildar R. Alembekov, Maria A. Lagarkova, Galina I. Kravatskaya, Vsevolod Y. Makeev, Yuri V. Kravatsky
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Cancers
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Online Access:https://www.mdpi.com/2072-6694/13/15/3889
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author Nickolai A. Tchurikov
Leonid A. Uroshlev
Elena S. Klushevskaya
Ildar R. Alembekov
Maria A. Lagarkova
Galina I. Kravatskaya
Vsevolod Y. Makeev
Yuri V. Kravatsky
author_facet Nickolai A. Tchurikov
Leonid A. Uroshlev
Elena S. Klushevskaya
Ildar R. Alembekov
Maria A. Lagarkova
Galina I. Kravatskaya
Vsevolod Y. Makeev
Yuri V. Kravatsky
author_sort Nickolai A. Tchurikov
collection DOAJ
description Endogenous hot spots of DNA double-strand breaks (DSBs) are tightly linked with transcription patterns and cancer. There are nine hot spots of DSBs (denoted Pleiades) in human rDNA units that are located exclusively inside the intergenic spacer (IGS). Profiles of Pleiades coincide with the profiles of γ-H2AX, suggesting a high level of in vivo breakage inside rDNA genes. The data were confirmed by microscopic observation of the largest γ-H2AX foci inside nucleoli in interphase chromosomes. Circular chromosome conformation capture (4C) data indicate that the rDNA units often make contact with a specific set of chromosomal regions containing genes that are involved in differentiation and cancer. Interestingly, these regions also often possess hot spots of DSBs that provide the potential for Robertsonian and oncogenic translocations. In this study, we searched for translocations in which rDNA clusters are involved. The whole genome sequence (WGS) data of normal T cells and NK-cell lymphomas from the same individuals revealed numerous translocations in which Pleiades were involved. The sites of these translocations in normal T cells and in the lymphomas were mostly different, although there were also some common sites. The genes at translocations in normal cells and in lymphomas are associated with predominantly non-overlapping lists of genes that are depleted with silenced genes. Our data indicate that rDNA-mediated translocations occur at about the same frequency in the normal T cells and NK-lymphoma cells but differ at particular sites that correspond to open chromatin. We conclude that oncogenic translocations lead to dysregulation of a specific set of genes controlling development. In normal T cells and in NK cells, there are hot spots of translocations at sites possessing strong H3K27ac marks. The data indicate that Pleiades are involved in rDNA-mediated translocation.
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spelling doaj.art-067a6060975641dda7efba25444fdb1f2023-11-22T05:29:34ZengMDPI AGCancers2072-66942021-08-011315388910.3390/cancers13153889Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBsNickolai A. Tchurikov0Leonid A. Uroshlev1Elena S. Klushevskaya2Ildar R. Alembekov3Maria A. Lagarkova4Galina I. Kravatskaya5Vsevolod Y. Makeev6Yuri V. Kravatsky7Engelhardt Institute of Molecular Biology Russian Academy of Sciences, 119334 Moscow, RussiaVavilov Institute of General Genetics Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology Russian Academy of Sciences, 119334 Moscow, RussiaEngelhardt Institute of Molecular Biology Russian Academy of Sciences, 119334 Moscow, RussiaFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, 119435 Moscow, RussiaEngelhardt Institute of Molecular Biology Russian Academy of Sciences, 119334 Moscow, RussiaEngelhardt Institute of Molecular Biology Russian Academy of Sciences, 119334 Moscow, RussiaEngelhardt Institute of Molecular Biology Russian Academy of Sciences, 119334 Moscow, RussiaEndogenous hot spots of DNA double-strand breaks (DSBs) are tightly linked with transcription patterns and cancer. There are nine hot spots of DSBs (denoted Pleiades) in human rDNA units that are located exclusively inside the intergenic spacer (IGS). Profiles of Pleiades coincide with the profiles of γ-H2AX, suggesting a high level of in vivo breakage inside rDNA genes. The data were confirmed by microscopic observation of the largest γ-H2AX foci inside nucleoli in interphase chromosomes. Circular chromosome conformation capture (4C) data indicate that the rDNA units often make contact with a specific set of chromosomal regions containing genes that are involved in differentiation and cancer. Interestingly, these regions also often possess hot spots of DSBs that provide the potential for Robertsonian and oncogenic translocations. In this study, we searched for translocations in which rDNA clusters are involved. The whole genome sequence (WGS) data of normal T cells and NK-cell lymphomas from the same individuals revealed numerous translocations in which Pleiades were involved. The sites of these translocations in normal T cells and in the lymphomas were mostly different, although there were also some common sites. The genes at translocations in normal cells and in lymphomas are associated with predominantly non-overlapping lists of genes that are depleted with silenced genes. Our data indicate that rDNA-mediated translocations occur at about the same frequency in the normal T cells and NK-lymphoma cells but differ at particular sites that correspond to open chromatin. We conclude that oncogenic translocations lead to dysregulation of a specific set of genes controlling development. In normal T cells and in NK cells, there are hot spots of translocations at sites possessing strong H3K27ac marks. The data indicate that Pleiades are involved in rDNA-mediated translocation.https://www.mdpi.com/2072-6694/13/15/3889NK-cell lymphomasT cellsrDNA genesinter-chromosomal contacts4Ctranslocations
spellingShingle Nickolai A. Tchurikov
Leonid A. Uroshlev
Elena S. Klushevskaya
Ildar R. Alembekov
Maria A. Lagarkova
Galina I. Kravatskaya
Vsevolod Y. Makeev
Yuri V. Kravatsky
Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs
Cancers
NK-cell lymphomas
T cells
rDNA genes
inter-chromosomal contacts
4C
translocations
title Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs
title_full Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs
title_fullStr Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs
title_full_unstemmed Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs
title_short Chromosomal Translocations in NK-Cell Lymphomas Originate from Inter-Chromosomal Contacts of Active rDNA Clusters Possessing Hot Spots of DSBs
title_sort chromosomal translocations in nk cell lymphomas originate from inter chromosomal contacts of active rdna clusters possessing hot spots of dsbs
topic NK-cell lymphomas
T cells
rDNA genes
inter-chromosomal contacts
4C
translocations
url https://www.mdpi.com/2072-6694/13/15/3889
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