Deep sequencing identifies circulating mouse miRNAs that are functionally implicated in manifestations of aging and

Joseph M Dhahbi1, Stephen R Spindler, Hani Atamna

  • 1Department of Biochemistry, University of California at Riverside, Riverside, CA 92521, USA. jdhahbi@ucr.edu

Aging
|March 9, 2013
PubMed

Insights

Circulating microRNAs (miRNAs) increase with age in mice, but calorie restriction (CR) can reverse this trend. These age-related miRNA changes are linked to aging processes and diseases.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Gerontology

Background:

  • MicroRNAs (miRNAs) regulate gene expression and cellular processes.
  • Circulating miRNAs mediate cell-to-cell communication.
  • Aging involves cellular changes potentially influenced by miRNAs.

Purpose of the Study:

  • To comprehensively assess the role of circulating miRNAs in the aging process.
  • To characterize circulating miRNAs in young, old, and calorie-restricted (CR) old mice using deep sequencing.

Main Methods:

  • Deep sequencing of serum miRNAs from young mice, old mice, and old mice on CR.
  • Identification of novel and quantification of known circulating miRNAs.

Main Results:

  • Many circulating miRNAs increase with age in mice.
  • Calorie restriction (CR) antagonizes age-related increases in circulating miRNAs.
  • Genes targeted by age-modulated miRNAs are involved in aging-related biological processes, including metabolic changes.

Conclusions:

  • Circulating miRNAs are implicated in the aging process.
  • Age-modulated miRNAs may play a functional role in aging-related metabolic changes.
  • Further research is needed on miRNA tissue of origin, cellular targets, and functional roles in aging.