Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people

Introduction: Mild cognitive impairments (MCI) accompanying aging are associated with oxidative stress. The ability of cells to respond to stress is determined by the protein synthesis level, which depends on the ribosomes number. Ribosomal deficit was documented in MCI. The number of ribosomes depe...

Full description

Bibliographic Details
Main Authors: Natalia N. Veiko, Elizaveta S. Ershova, Roman V. Veiko, Pavel E. Umriukhin, Marat V. Kurmyshev, Georg P. Kostyuk, Sergey I. Kutsev, Svetlana V. Kostyuk
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2022.967448/full
_version_ 1797994944333348864
author Natalia N. Veiko
Elizaveta S. Ershova
Elizaveta S. Ershova
Roman V. Veiko
Pavel E. Umriukhin
Pavel E. Umriukhin
Pavel E. Umriukhin
Marat V. Kurmyshev
Georg P. Kostyuk
Sergey I. Kutsev
Svetlana V. Kostyuk
Svetlana V. Kostyuk
author_facet Natalia N. Veiko
Elizaveta S. Ershova
Elizaveta S. Ershova
Roman V. Veiko
Pavel E. Umriukhin
Pavel E. Umriukhin
Pavel E. Umriukhin
Marat V. Kurmyshev
Georg P. Kostyuk
Sergey I. Kutsev
Svetlana V. Kostyuk
Svetlana V. Kostyuk
author_sort Natalia N. Veiko
collection DOAJ
description Introduction: Mild cognitive impairments (MCI) accompanying aging are associated with oxidative stress. The ability of cells to respond to stress is determined by the protein synthesis level, which depends on the ribosomes number. Ribosomal deficit was documented in MCI. The number of ribosomes depends, together with other factors, on the number of ribosomal genes copies. We hypothesized that MCI is associated with low rDNA CN in the elderly person genome.Materials and Methods: rDNA CN and the telomere repeat (TR) content were determined in the DNA of peripheral blood leukocytes of 93 elderly people (61–91 years old) with MCI and 365 healthy volunteers (16–91 years old). The method of non-radioactive quantitative hybridization of DNA with biotinylated DNA probes was used for the analysis.Results: In the MCI group, rDNA CN (mean 329 ± 60; median 314 copies, n = 93) was significantly reduced (p < 10–15) compared to controls of the same age with preserved cognitive functions (mean 412 ± 79; median 401 copies, n = 168) and younger (16–60 years) control group (mean 426 ± 109; median 416 copies, n = 197). MCI is also associated with a decrease in TR DNA content. There is no correlation between the content of rDNA and TR in DNA, however, in the group of DNA samples with rDNA CN > 540, TR content range was significantly narrowed compared to the rest of the sample.Conclusion: Mild cognitive impairment is associated with low ribosomal genes copies in the elderly people genomes. A low level of rDNA CN may be one of the causes of ribosomal deficit that was documented in MCI. The potential possibilities of using the rDNA CN indicator as a prognostic marker characterizing human life expectancy are discussed.
first_indexed 2024-04-11T09:53:46Z
format Article
id doaj.art-2469864b4a2c4dc3b31bfb3bca208572
institution Directory Open Access Journal
issn 1664-8021
language English
last_indexed 2024-04-11T09:53:46Z
publishDate 2022-09-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Genetics
spelling doaj.art-2469864b4a2c4dc3b31bfb3bca2085722022-12-22T04:30:42ZengFrontiers Media S.A.Frontiers in Genetics1664-80212022-09-011310.3389/fgene.2022.967448967448Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly peopleNatalia N. Veiko0Elizaveta S. Ershova1Elizaveta S. Ershova2Roman V. Veiko3Pavel E. Umriukhin4Pavel E. Umriukhin5Pavel E. Umriukhin6Marat V. Kurmyshev7Georg P. Kostyuk8Sergey I. Kutsev9Svetlana V. Kostyuk10Svetlana V. Kostyuk11Research Centre for Medical Genetics (RCMG), Moscow, RussiaResearch Centre for Medical Genetics (RCMG), Moscow, RussiaFederal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, V.A. Negovsky Research Institute of General Reanimatology, Moscow, RussiaResearch Centre for Medical Genetics (RCMG), Moscow, RussiaResearch Centre for Medical Genetics (RCMG), Moscow, RussiaI.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, RussiaP.K. Anokhin Institute of Normal Physiology, Moscow, RussiaMental-health Clinic No1 Named After N.A. Alexeev, Moscow, RussiaMental-health Clinic No1 Named After N.A. Alexeev, Moscow, RussiaResearch Centre for Medical Genetics (RCMG), Moscow, RussiaResearch Centre for Medical Genetics (RCMG), Moscow, RussiaFederal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, V.A. Negovsky Research Institute of General Reanimatology, Moscow, RussiaIntroduction: Mild cognitive impairments (MCI) accompanying aging are associated with oxidative stress. The ability of cells to respond to stress is determined by the protein synthesis level, which depends on the ribosomes number. Ribosomal deficit was documented in MCI. The number of ribosomes depends, together with other factors, on the number of ribosomal genes copies. We hypothesized that MCI is associated with low rDNA CN in the elderly person genome.Materials and Methods: rDNA CN and the telomere repeat (TR) content were determined in the DNA of peripheral blood leukocytes of 93 elderly people (61–91 years old) with MCI and 365 healthy volunteers (16–91 years old). The method of non-radioactive quantitative hybridization of DNA with biotinylated DNA probes was used for the analysis.Results: In the MCI group, rDNA CN (mean 329 ± 60; median 314 copies, n = 93) was significantly reduced (p < 10–15) compared to controls of the same age with preserved cognitive functions (mean 412 ± 79; median 401 copies, n = 168) and younger (16–60 years) control group (mean 426 ± 109; median 416 copies, n = 197). MCI is also associated with a decrease in TR DNA content. There is no correlation between the content of rDNA and TR in DNA, however, in the group of DNA samples with rDNA CN > 540, TR content range was significantly narrowed compared to the rest of the sample.Conclusion: Mild cognitive impairment is associated with low ribosomal genes copies in the elderly people genomes. A low level of rDNA CN may be one of the causes of ribosomal deficit that was documented in MCI. The potential possibilities of using the rDNA CN indicator as a prognostic marker characterizing human life expectancy are discussed.https://www.frontiersin.org/articles/10.3389/fgene.2022.967448/fullribosomal genesrDNAagingrDNA CNmild cognitive impairment
spellingShingle Natalia N. Veiko
Elizaveta S. Ershova
Elizaveta S. Ershova
Roman V. Veiko
Pavel E. Umriukhin
Pavel E. Umriukhin
Pavel E. Umriukhin
Marat V. Kurmyshev
Georg P. Kostyuk
Sergey I. Kutsev
Svetlana V. Kostyuk
Svetlana V. Kostyuk
Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
Frontiers in Genetics
ribosomal genes
rDNA
aging
rDNA CN
mild cognitive impairment
title Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
title_full Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
title_fullStr Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
title_full_unstemmed Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
title_short Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
title_sort mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people
topic ribosomal genes
rDNA
aging
rDNA CN
mild cognitive impairment
url https://www.frontiersin.org/articles/10.3389/fgene.2022.967448/full
work_keys_str_mv AT natalianveiko mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT elizavetasershova mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT elizavetasershova mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT romanvveiko mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT paveleumriukhin mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT paveleumriukhin mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT paveleumriukhin mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT maratvkurmyshev mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT georgpkostyuk mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT sergeyikutsev mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT svetlanavkostyuk mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople
AT svetlanavkostyuk mildcognitiveimpairmentisassociatedwithlowcopynumberofribosomalgenesinthegenomesofelderlypeople