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Association of genetic variations in the mitochondrial DNA control region with presbycusis
BACKGROUND: The prominent role of mitochondria in the generation of reactive oxygen species, cell death, and energy production contributes to the importance of this organelle in the intracellular mechanism underlying the progression of the common sensory disorder of the elderly, presbycusis. Reduced...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344408/ https://www.ncbi.nlm.nih.gov/pubmed/28424544 http://dx.doi.org/10.2147/CIA.S123278 |
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author | Falah, Masoumeh Farhadi, Mohammad Kamrava, Seyed Kamran Mahmoudian, Saeid Daneshi, Ahmad Balali, Maryam Asghari, Alimohamad Houshmand, Massoud |
author_facet | Falah, Masoumeh Farhadi, Mohammad Kamrava, Seyed Kamran Mahmoudian, Saeid Daneshi, Ahmad Balali, Maryam Asghari, Alimohamad Houshmand, Massoud |
author_sort | Falah, Masoumeh |
collection | PubMed |
description | BACKGROUND: The prominent role of mitochondria in the generation of reactive oxygen species, cell death, and energy production contributes to the importance of this organelle in the intracellular mechanism underlying the progression of the common sensory disorder of the elderly, presbycusis. Reduced mitochondrial DNA (mtDNA) gene expression and coding region variation have frequently been reported as being associated with the development of presbycusis. The mtDNA control region regulates gene expression and replication of the genome of this organelle. To comprehensively understand of the role of mitochondria in the progression of presbycusis, we compared variations in the mtDNA control region between subjects with presbycusis and controls. METHODS: A total of 58 presbycusis patients and 220 control subjects were enrolled in the study after examination by the otolaryngologist and audiology tests. Variations in the mtDNA control region were investigated by polymerase chain reaction and Sanger sequencing. RESULTS: A total of 113 sequence variants were observed in mtDNA, and variants were detected in 100% of patients, with 84% located in hypervariable regions. The frequencies of the variants, 16,223 C>T, 16,311 T>C, 16,249 T>C, and 15,954 A>C, were significantly different between presbycusis and control subjects. CONCLUSION: The statistically significant difference in the frequencies of four nucleotide variants in the mtDNA control region of presbycusis patients and controls is in agreement with previous experimental evidence and supports the role of mitochondria in the intracellular mechanism underlying presbycusis development. Moreover, these variants have potential as diagnostic markers for individuals at a high risk of developing presbycusis. The data also suggest the possible presence of changes in the mtDNA control region in presbycusis, which could alter regulatory factor binding sites and influence mtDNA gene expression and copy number. |
format | Online Article Text |
id | pubmed-5344408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53444082017-04-19 Association of genetic variations in the mitochondrial DNA control region with presbycusis Falah, Masoumeh Farhadi, Mohammad Kamrava, Seyed Kamran Mahmoudian, Saeid Daneshi, Ahmad Balali, Maryam Asghari, Alimohamad Houshmand, Massoud Clin Interv Aging Original Research BACKGROUND: The prominent role of mitochondria in the generation of reactive oxygen species, cell death, and energy production contributes to the importance of this organelle in the intracellular mechanism underlying the progression of the common sensory disorder of the elderly, presbycusis. Reduced mitochondrial DNA (mtDNA) gene expression and coding region variation have frequently been reported as being associated with the development of presbycusis. The mtDNA control region regulates gene expression and replication of the genome of this organelle. To comprehensively understand of the role of mitochondria in the progression of presbycusis, we compared variations in the mtDNA control region between subjects with presbycusis and controls. METHODS: A total of 58 presbycusis patients and 220 control subjects were enrolled in the study after examination by the otolaryngologist and audiology tests. Variations in the mtDNA control region were investigated by polymerase chain reaction and Sanger sequencing. RESULTS: A total of 113 sequence variants were observed in mtDNA, and variants were detected in 100% of patients, with 84% located in hypervariable regions. The frequencies of the variants, 16,223 C>T, 16,311 T>C, 16,249 T>C, and 15,954 A>C, were significantly different between presbycusis and control subjects. CONCLUSION: The statistically significant difference in the frequencies of four nucleotide variants in the mtDNA control region of presbycusis patients and controls is in agreement with previous experimental evidence and supports the role of mitochondria in the intracellular mechanism underlying presbycusis development. Moreover, these variants have potential as diagnostic markers for individuals at a high risk of developing presbycusis. The data also suggest the possible presence of changes in the mtDNA control region in presbycusis, which could alter regulatory factor binding sites and influence mtDNA gene expression and copy number. Dove Medical Press 2017-03-03 /pmc/articles/PMC5344408/ /pubmed/28424544 http://dx.doi.org/10.2147/CIA.S123278 Text en © 2017 Falah et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Falah, Masoumeh Farhadi, Mohammad Kamrava, Seyed Kamran Mahmoudian, Saeid Daneshi, Ahmad Balali, Maryam Asghari, Alimohamad Houshmand, Massoud Association of genetic variations in the mitochondrial DNA control region with presbycusis |
title | Association of genetic variations in the mitochondrial DNA control region with presbycusis |
title_full | Association of genetic variations in the mitochondrial DNA control region with presbycusis |
title_fullStr | Association of genetic variations in the mitochondrial DNA control region with presbycusis |
title_full_unstemmed | Association of genetic variations in the mitochondrial DNA control region with presbycusis |
title_short | Association of genetic variations in the mitochondrial DNA control region with presbycusis |
title_sort | association of genetic variations in the mitochondrial dna control region with presbycusis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344408/ https://www.ncbi.nlm.nih.gov/pubmed/28424544 http://dx.doi.org/10.2147/CIA.S123278 |
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