circRNAs expressed in human peripheral blood are associated with human aging phenotypes, cellular senescence and mouse lifespan
Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the observation that circRNAs are known to accumulate in older organisms and have been reported in cellular senescence, their role in aging remains relat...
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Published in | GeroScience Vol. 42; no. 1; pp. 183 - 199 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.02.2020
|
Subjects | |
Online Access | Get full text |
ISSN | 2509-2715 2509-2723 2509-2723 |
DOI | 10.1007/s11357-019-00120-z |
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Abstract | Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the observation that circRNAs are known to accumulate in older organisms and have been reported in cellular senescence, their role in aging remains relatively unexplored. Here, we have assessed circRNA expression in aging human blood and followed up age-associated circRNA in relation to human aging phenotypes, mammalian longevity as measured by mouse median strain lifespan and cellular senescence in four different primary human cell types. We found that circRNAs
circDEF6
, c
ircEP300
,
circFOXO3
and
circFNDC3B
demonstrate associations with parental longevity or hand grip strength in 306 subjects from the InCHIANTI study of aging, and furthermore,
circFOXO3
and
circEP300
also demonstrate differential expression in one or more human senescent cell types. Finally, four circRNAs tested showed evidence of conservation in mouse. Expression levels of one of these,
circPlekhm1
, was nominally associated with lifespan. These data suggest that circRNA may represent a novel class of regulatory RNA involved in the determination of aging phenotypes, which may show future promise as both biomarkers and future therapeutic targets for age-related disease. |
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AbstractList | Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the observation that circRNAs are known to accumulate in older organisms and have been reported in cellular senescence, their role in aging remains relatively unexplored. Here, we have assessed circRNA expression in aging human blood and followed up age-associated circRNA in relation to human aging phenotypes, mammalian longevity as measured by mouse median strain lifespan and cellular senescence in four different primary human cell types. We found that circRNAs circDEF6, circEP300, circFOXO3 and circFNDC3B demonstrate associations with parental longevity or hand grip strength in 306 subjects from the InCHIANTI study of aging, and furthermore, circFOXO3 and circEP300 also demonstrate differential expression in one or more human senescent cell types. Finally, four circRNAs tested showed evidence of conservation in mouse. Expression levels of one of these, circPlekhm1, was nominally associated with lifespan. These data suggest that circRNA may represent a novel class of regulatory RNA involved in the determination of aging phenotypes, which may show future promise as both biomarkers and future therapeutic targets for age-related disease.Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the observation that circRNAs are known to accumulate in older organisms and have been reported in cellular senescence, their role in aging remains relatively unexplored. Here, we have assessed circRNA expression in aging human blood and followed up age-associated circRNA in relation to human aging phenotypes, mammalian longevity as measured by mouse median strain lifespan and cellular senescence in four different primary human cell types. We found that circRNAs circDEF6, circEP300, circFOXO3 and circFNDC3B demonstrate associations with parental longevity or hand grip strength in 306 subjects from the InCHIANTI study of aging, and furthermore, circFOXO3 and circEP300 also demonstrate differential expression in one or more human senescent cell types. Finally, four circRNAs tested showed evidence of conservation in mouse. Expression levels of one of these, circPlekhm1, was nominally associated with lifespan. These data suggest that circRNA may represent a novel class of regulatory RNA involved in the determination of aging phenotypes, which may show future promise as both biomarkers and future therapeutic targets for age-related disease. Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the observation that circRNAs are known to accumulate in older organisms and have been reported in cellular senescence, their role in aging remains relatively unexplored. Here, we have assessed circRNA expression in aging human blood and followed up age-associated circRNA in relation to human aging phenotypes, mammalian longevity as measured by mouse median strain lifespan and cellular senescence in four different primary human cell types. We found that circRNAs circDEF6 , c ircEP300 , circFOXO3 and circFNDC3B demonstrate associations with parental longevity or hand grip strength in 306 subjects from the InCHIANTI study of aging, and furthermore, circFOXO3 and circEP300 also demonstrate differential expression in one or more human senescent cell types. Finally, four circRNAs tested showed evidence of conservation in mouse. Expression levels of one of these, circPlekhm1 , was nominally associated with lifespan. These data suggest that circRNA may represent a novel class of regulatory RNA involved in the determination of aging phenotypes, which may show future promise as both biomarkers and future therapeutic targets for age-related disease. Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the observation that circRNAs are known to accumulate in older organisms and have been reported in cellular senescence, their role in aging remains relatively unexplored. Here, we have assessed circRNA expression in aging human blood and followed up age-associated circRNA in relation to human aging phenotypes, mammalian longevity as measured by mouse median strain lifespan and cellular senescence in four different primary human cell types. We found that circRNAs circDEF6, circEP300, circFOXO3 and circFNDC3B demonstrate associations with parental longevity or hand grip strength in 306 subjects from the InCHIANTI study of aging, and furthermore, circFOXO3 and circEP300 also demonstrate differential expression in one or more human senescent cell types. Finally, four circRNAs tested showed evidence of conservation in mouse. Expression levels of one of these, circPlekhm1, was nominally associated with lifespan. These data suggest that circRNA may represent a novel class of regulatory RNA involved in the determination of aging phenotypes, which may show future promise as both biomarkers and future therapeutic targets for age-related disease. |
Author | Peters, Luanne L. Haque, Shahnaz Bandinelli, Stefania Ames, Ryan M. Harries, Lorna W. Moore, Karen Pilling, Luke C. Ferrucci, Luigi |
Author_xml | – sequence: 1 givenname: Shahnaz surname: Haque fullname: Haque, Shahnaz organization: RNA-Mediated Mechanisms of Disease Group, Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter – sequence: 2 givenname: Ryan M. surname: Ames fullname: Ames, Ryan M. organization: Biosciences, University of Exeter – sequence: 3 givenname: Karen surname: Moore fullname: Moore, Karen organization: College of Life and Environmental Sciences, University of Exeter – sequence: 4 givenname: Luke C. surname: Pilling fullname: Pilling, Luke C. organization: Epidemiology and Public Health, University of Exeter Medical School, University of Exeter – sequence: 5 givenname: Luanne L. surname: Peters fullname: Peters, Luanne L. organization: The Jackson Laboratory Nathan Shock Centre of Excellence in the Basic Biology of Aging – sequence: 6 givenname: Stefania surname: Bandinelli fullname: Bandinelli, Stefania organization: Geriatric Unit, USL Toscana Centro – sequence: 7 givenname: Luigi surname: Ferrucci fullname: Ferrucci, Luigi organization: National Institute on Aging, Clinical Research Branch, Harbor Hospital – sequence: 8 givenname: Lorna W. orcidid: 0000-0001-7791-8061 surname: Harries fullname: Harries, Lorna W. email: L.W.Harries@exeter.ac.uk organization: RNA-Mediated Mechanisms of Disease Group, Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31811527$$D View this record in MEDLINE/PubMed |
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Keywords | Circular RNA Aging phenotypes Senescence Median strain lifespan |
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Snippet | Circular RNAs (circRNAs) are an emerging class of non-coding RNA molecules that are thought to regulate gene expression and human disease. Despite the... |
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SubjectTerms | Aged Aging - genetics Animals Biomedical and Life Sciences Cell Biology Cellular Senescence - genetics Geriatrics/Gerontology Hand Strength Humans Life Sciences Longevity - genetics Mice MicroRNAs Molecular Medicine Original Original Article Phenotype RNA, Circular |
Title | circRNAs expressed in human peripheral blood are associated with human aging phenotypes, cellular senescence and mouse lifespan |
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