Language
English
Publication Date
10-1-2025
Journal
Medical Review (2021)
DOI
10.1515/mr-2025-0032
PMID
41158292
PMCID
PMC12558037
PubMedCentral® Posted Date
8-27-2025
PubMedCentral® Full Text Version
Post-print
Abstract
Increased transcript diversity, which is caused in part by alternative splicing and cryptic transcription, is an underappreciated aspect of age-associated transcriptome remodeling. Recent work has revealed that structurally novel transcripts increase during aging in many tissues. Genes with cryptic and alternatively spliced transcripts with age are enriched for functional categories relevant to tissue function and aging, and have been implicated in cognitive decline, decreased muscle strength, reduced oocyte quality, immune aging, altered stem cell properties, and senescence. Indeed, there is emerging evidence that alternatively spliced transcripts and elevated cryptic transcription directly contribute to aging phenotypes in multiple tissues. The full impact of the increased transcript diversity on the aging process has yet to be explored. The increased transcript diversity engendered by alternative splicing and cryptic transcription is emerging as a potent driver of aging and aging phenotypes, adding another layer to our understanding of the transcriptional regulation of aging.
Keywords
aging, alternative splicing, cryptic transcription, epigenetics
Published Open-Access
yes
Recommended Citation
Brenna S McCauley, Nicholas Nikoloutsos, and Weiwei Dang, "Transcript Diversity in Aging: Cryptic Transcription and Splicing" (2025). Faculty and Staff Publications. 5031.
https://digitalcommons.library.tmc.edu/baylor_docs/5031
Included in
Genetic Phenomena Commons, Genetic Processes Commons, Genetic Structures Commons, Medical Genetics Commons, Medical Molecular Biology Commons, Medical Specialties Commons