AI Article Synopsis

  • Cardiovascular disease (CVD) is a major global health issue largely influenced by aging, and understanding gene expression networks in this context is crucial.
  • The review focuses on significant RNA modifications that impact both mRNAs and non-coding RNAs during aging, highlighting their roles in various CVDs such as atherosclerosis and hypertension.
  • It also covers detection methods and bioinformatics tools used to study these RNA modifications, emphasizing their relevance in aging-related cardiovascular diseases.

Article Abstract

Cardiovascular disease (CVD) is a leading cause of morbidity and mortality worldwide that bears an enormous healthcare burden and aging is a major contributing factor to CVDs. Functional gene expression network during aging is regulated by mRNAs transcriptionally and by non-coding RNAs epi-transcriptionally. RNA modifications alter the stability and function of both mRNAs and non-coding RNAs and are involved in differentiation, development, and diseases. Here we review major chemical RNA modifications on mRNAs and non-coding RNAs, including N6-adenosine methylation, N1-adenosine methylation, 5-methylcytidine, pseudouridylation, 2' -O-ribose-methylation, and N7-methylguanosine, in the aging process with an emphasis on cardiovascular aging. We also summarize the currently available methods to detect RNA modifications and the bioinformatic tools to study RNA modifications. More importantly, we discussed the specific implication of the RNA modifications on mRNAs and non-coding RNAs in the pathogenesis of aging-associated CVDs, including atherosclerosis, hypertension, coronary heart diseases, congestive heart failure, atrial fibrillation, peripheral artery disease, venous insufficiency, and stroke.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596201PMC
http://dx.doi.org/10.18632/aging.204311DOI Listing

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