PUBLICATION

Age-Associated Different Transcriptome Profiling in Zebrafish and Rats: an Insight into the Diversity of Vertebrate Aging

Authors
Kijima, Y., Wantong, W., Igarashi, Y., Yoshitake, K., Asakawa, S., Suzuki, Y., Watabe, S., Kinoshita, S.
ID
ZDB-PUB-220907-15
Date
2022
Source
Marine biotechnology (New York, N.Y.)   24(5): 895-910 (Journal)
Registered Authors
Kinoshita, Shigeharu, Watabe, Shugo
Keywords
AP-1, Comparative transcriptome, Hmgb, Mammal, Senescence, Teleost
MeSH Terms
  • Aging/genetics
  • Animals
  • Collagen
  • Gene Expression Profiling
  • Humans
  • Mammals/genetics
  • RNA
  • Rats
  • Transcription Factor AP-1*/genetics
  • Transcriptome
  • Zebrafish*/genetics
PubMed
36063238 Full text @ Mar. Biotechnol.
Abstract
Most mammals, including humans, show obvious aging phenotypes, for example, loss of tissue plasticity and sarcopenia. In this regard, fish can be attractive models to study senescence because of their unique aging characteristics. The lifespan of fish varies widely, and several species can live for over 200 years. Moreover, some fish show anti-aging features and indeterminate growth throughout their life. Therefore, exploring the aging mechanism in fish could provide new insights into vertebrate aging. To this end, we conducted RNA sequencing (RNA-seq) assays for various organs and growth stages of zebrafish and compared the data with previously published RNA-seq data of rats. Age-associated differentially expressed genes (DEGs) for all zebrafish tissue samples reveal the upregulation of circadian genes and downregulation of hmgb3a. On one hand, a comparative analysis of DEG profiles associated with aging between zebrafish and rats identifies upregulation of circadian genes and downregulation of collagen genes as conserved transcriptome changes. On the other hand, in zebrafish, upregulation of autophagy-related genes in muscles and AP-1 transcription factor genes in various tissues is observed, which may imply fish-specific anti-aging characteristics. Consistent with our knowledge of mammalian aging, DEG profiles related to tissue senescence are observed in rats. We also detect age-associated downregulation of muscle homeostasis and differentiation-related genes in zebrafish gills, indicating a fish-specific senescence phenotype. Our results indicate both common and different aging profiles between fish and mammals, which could be used for future translational research.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping