The Psychoemotional Stress-Induced Changes in the Abundance of SatIII (1q12) and Telomere Repeats, but Not Ribosomal DNA, in Human Leukocytes

• Published in: Genes 2022-02, Vol.13 (2), p.343
• Main Authors: Umriukhin, Pavel E, Ershova, Elizaveta S, Filev, Anton D, Agafonova, Oksana N, Martynov, Andrey V, Zakharova, Natalia V, Veiko, Roman V, Porokhovnik, Lev N, Kostyuk, George P, Kutsev, Sergey I, Veiko, Natalia N, Kostyuk, Svetlana V
• Format: Article
• Language: English
• Subjects: Aging; Brain; Chromosomes; Copy number; Deoxyribonucleic acid; DNA; DNA Copy Number Variations; DNA probes; DNA, Ribosomal - genetics; Emotions; Flow cytometry; Genetic disorders; Genomes; Hospitalization; Humans; Hybridization; Leukocytes; Lymphocytes; Medical research; Medical students; Mental disorders; NOX4 protein; Oxidative stress; Patients; Physiology; Quantitation; Ribosomal DNA; Schizophrenia; Schizophrenia - genetics; Telomere - genetics; Telomeres
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes13020343

As shown earlier, copy number variations (CNV) in the human satellite III (1q12) fragment (f-SatIII) and the telomere repeat (TR) reflects the cell's response to oxidative stress. The contents of f-SatIII and TR in schizophrenic (SZ) patients were found to be lower than in healthy controls (HC) in previous studies. The major question of this study was: 'What are the f-SatIII and TR CNV dynamic changes in human leukocytes, depending on psychoemotional stress?' We chose a model of psychoemotional stress experienced by second-year medical students during their exams. Blood samples were taken in stressful conditions (exams) and in a control non-stressful period. Biotinylated probes were used for f-SatIII, rDNA, and TR quantitation in leukocyte DNA by non-radioactive quantitative hybridization in SZ patients ( = 97), HC ( = 97), and medical students ( = 17, = 42). A flow cytometry analysis was used for the oxidative stress marker (NOX4, 8-oxodG, and γH2AX) detection in the lymphocytes of the three groups. Oxidative stress markers increased significantly in the students' lymphocytes during psychoemotional stress. The TR and f-SatIII, but not the rDNA, contents significantly changed in the DNA isolated from human blood leukocytes. After a restoration period (post-examinational vacations), the f-SatIII content decreased, and the TR content increased. Changes in the blood cells of students during examinational stress were similar to those in SZ patients during an exacerbation of the disease. Psychoemotional stress in students during exams triggers a universal mechanism of oxidative stress. The oxidative stress causes significant changes in the f-SatIII and TR contents, while the ribosomal repeat content remains stable. A hypothesis is proposed to explain the quantitative polymorphisms of f-SatIII and TR contents under transient (e.g., students' exams) or chronic (in SZ patients) stress. The changes in the f-SatIII and TR copy numbers are non-specific events, irrespective of the source of stress. Thus, our findings suggest that the psychoemotional stress, common in SZ patients and healthy students during exams, but not in a schizophrenia-specific event, was responsible for the changes in the repeat contents that we observed earlier in SZ patients.