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Copy Number Variation of Human Satellite III (1q12) With Aging

Introduction: Human satellite DNA is organized in long arrays in peri/centromeric heterochromatin. There is little information about satellite copy number variants (CNVs) in aging and replicative cell senescence (RS). Materials and Methods: Biotinylated pUC1.77 probe was used for the satellite III (...

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Autores principales: Ershova, Elizaveta S., Malinovskaya, Elena M., Konkova, Marina S., Veiko, Roman V., Umriukhin, Pavel E., Martynov, Andrey V., Kutsev, Sergey I., Veiko, Natalia N., Kostyuk, Svetlana V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692473/
https://www.ncbi.nlm.nih.gov/pubmed/31447880
http://dx.doi.org/10.3389/fgene.2019.00704
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author Ershova, Elizaveta S.
Malinovskaya, Elena M.
Konkova, Marina S.
Veiko, Roman V.
Umriukhin, Pavel E.
Martynov, Andrey V.
Kutsev, Sergey I.
Veiko, Natalia N.
Kostyuk, Svetlana V.
author_facet Ershova, Elizaveta S.
Malinovskaya, Elena M.
Konkova, Marina S.
Veiko, Roman V.
Umriukhin, Pavel E.
Martynov, Andrey V.
Kutsev, Sergey I.
Veiko, Natalia N.
Kostyuk, Svetlana V.
author_sort Ershova, Elizaveta S.
collection PubMed
description Introduction: Human satellite DNA is organized in long arrays in peri/centromeric heterochromatin. There is little information about satellite copy number variants (CNVs) in aging and replicative cell senescence (RS). Materials and Methods: Biotinylated pUC1.77 probe was used for the satellite III (f-SatIII) quantitation in leukocyte DNA by the non-radioactive quantitative hybridization for 557 subjects between 2 and 91 years old. The effect of RS and genotoxic stress (GS, 4 or 6 µM of K(2)CrO(4)) on the f-SatIII CNV was studied on the cultured human skin fibroblast (HSF) lines of five subjects. Results: f-SatIII in leukocyte and HSFs varies between 5.7 and 40 pg/ng of DNA. During RS, the f-SatIII content in HSFs increased. During GS, HSFs may increase or decrease f-SatIII content. Cells with low f-SatIII content have the greatest proliferative potential. F-SatIII CNVs in different individuals belonging to the different generations depend on year of their birth. Children (born in 2005–2015 years) differed significantly from the other age groups by low content and low coefficient of variation of f-SatIII. In the individuals born in 1912–1925 and living in unfavorable social conditions (FWW, the Revolution and the Russian Civil War, SWW), there is a significant disproportion in the content of f-SatIII. The coefficient of variation reaches the maximum values than in individuals born in the period from 1926 to 1975. In the group of people born in 1990–2000 (Chernobyl disaster, the collapse of the Soviet Union, and a sharp decline in the population living standard), again, there is a significant disproportion of individuals in the content of f-SatIII. A similar disproportion was observed in the analysis of a group of individuals born in 1926–1975 who in their youth worked for a long time in high-radioactive environment. Conclusion: In generations that were born and who lived in childhood in a period of severe social perturbations or in conditions of environmental pollution, we found a significant increase in leukocyte DNA f-SatIII variability. It is hypothesized that the change of the f-SatIII content in the blood cells reflects the body response to stress of different nature and intensity.
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spelling pubmed-66924732019-08-23 Copy Number Variation of Human Satellite III (1q12) With Aging Ershova, Elizaveta S. Malinovskaya, Elena M. Konkova, Marina S. Veiko, Roman V. Umriukhin, Pavel E. Martynov, Andrey V. Kutsev, Sergey I. Veiko, Natalia N. Kostyuk, Svetlana V. Front Genet Genetics Introduction: Human satellite DNA is organized in long arrays in peri/centromeric heterochromatin. There is little information about satellite copy number variants (CNVs) in aging and replicative cell senescence (RS). Materials and Methods: Biotinylated pUC1.77 probe was used for the satellite III (f-SatIII) quantitation in leukocyte DNA by the non-radioactive quantitative hybridization for 557 subjects between 2 and 91 years old. The effect of RS and genotoxic stress (GS, 4 or 6 µM of K(2)CrO(4)) on the f-SatIII CNV was studied on the cultured human skin fibroblast (HSF) lines of five subjects. Results: f-SatIII in leukocyte and HSFs varies between 5.7 and 40 pg/ng of DNA. During RS, the f-SatIII content in HSFs increased. During GS, HSFs may increase or decrease f-SatIII content. Cells with low f-SatIII content have the greatest proliferative potential. F-SatIII CNVs in different individuals belonging to the different generations depend on year of their birth. Children (born in 2005–2015 years) differed significantly from the other age groups by low content and low coefficient of variation of f-SatIII. In the individuals born in 1912–1925 and living in unfavorable social conditions (FWW, the Revolution and the Russian Civil War, SWW), there is a significant disproportion in the content of f-SatIII. The coefficient of variation reaches the maximum values than in individuals born in the period from 1926 to 1975. In the group of people born in 1990–2000 (Chernobyl disaster, the collapse of the Soviet Union, and a sharp decline in the population living standard), again, there is a significant disproportion of individuals in the content of f-SatIII. A similar disproportion was observed in the analysis of a group of individuals born in 1926–1975 who in their youth worked for a long time in high-radioactive environment. Conclusion: In generations that were born and who lived in childhood in a period of severe social perturbations or in conditions of environmental pollution, we found a significant increase in leukocyte DNA f-SatIII variability. It is hypothesized that the change of the f-SatIII content in the blood cells reflects the body response to stress of different nature and intensity. Frontiers Media S.A. 2019-08-07 /pmc/articles/PMC6692473/ /pubmed/31447880 http://dx.doi.org/10.3389/fgene.2019.00704 Text en Copyright © 2019 Ershova, Malinovskaya, Konkova, Veiko, Umriukhin, Martynov, Kutsev, Veiko and Kostyuk http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Ershova, Elizaveta S.
Malinovskaya, Elena M.
Konkova, Marina S.
Veiko, Roman V.
Umriukhin, Pavel E.
Martynov, Andrey V.
Kutsev, Sergey I.
Veiko, Natalia N.
Kostyuk, Svetlana V.
Copy Number Variation of Human Satellite III (1q12) With Aging
title Copy Number Variation of Human Satellite III (1q12) With Aging
title_full Copy Number Variation of Human Satellite III (1q12) With Aging
title_fullStr Copy Number Variation of Human Satellite III (1q12) With Aging
title_full_unstemmed Copy Number Variation of Human Satellite III (1q12) With Aging
title_short Copy Number Variation of Human Satellite III (1q12) With Aging
title_sort copy number variation of human satellite iii (1q12) with aging
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692473/
https://www.ncbi.nlm.nih.gov/pubmed/31447880
http://dx.doi.org/10.3389/fgene.2019.00704
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