Skip to main content
Log in

Spermine and gene methylation: a mechanism of lifespan extension induced by polyamine-rich diet

  • Minireview Article
  • Published:
Amino Acids Aims and scope Submit manuscript

Abstract

The polyamines spermidine and spermine are synthesized in almost all organisms and are also contained in food. Polyamine synthesis decreases with aging, but no significant decrease in polyamine concentrations were found in organs, tissues, and blood of adult animals and humans. We found that healthy dietary patterns were associated with a preference for polyamine-rich foods, and first reported that increased polyamine intake extended the lifespan of mice and decreased the incidence of colon cancer induced by repeated administration of moderate amounts of a carcinogen. Recent investigations have revealed that changes in DNA methylation status play an important role in lifespan and aging-associated pathologies. The methylation of DNA is regulated by DNA methyltransferases in the presence of S-adenosylmethionine. Decarboxylated S-adenosylmethionine, converted from S-adenosylmethionine by S-adenosylmethionine decarboxylase, provides an aminopropyl group to synthesize spermine and spermidine and acts to inhibit DNMT activity. Long-term increased polyamine intake were shown to elevate blood spermine levels in mice and humans. In vitro studies demonstrated that spermine reversed changes induced by the inhibition of ornithine decarboxylase (e.g., increased decarboxylated S-adenosylmethionine, decreased DNA methyltransferase activity, increased aberrant DNA methylation), whose activity decreases with aging. Further, aged mice fed high-polyamine chow demonstrated suppression of aberrant DNA methylation and a consequent increase in protein levels of lymphocyte function-associated antigen 1, which plays a pivotal role on inflammatory process. This review discusses the relation between polyamine metabolism and DNA methylation, as well as the biological mechanism of lifespan extension induced by increased polyamine intake.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Abbreviations

LFA-1:

Lymphocyte function-associated antigen 1

ODC:

Ornithine decarboxylase

CVDs:

Cardiovascular diseases

SAM:

S-Adenosylmethionine

DNMT:

DNA methyltransferase

dcSAM:

Decarboxylated S-adenosylmethionine

ATP:

Adenosine triphosphate

AdoMetDC:

S-Adenosylmethionine decarboxylase

ODC-AZ:

Ornithine decarboxylase antizyme

DFMO:

α-d,l-Difluoromethylornithine hydrochloride

References

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kuniyasu Soda.

Ethics declarations

Conflict of interest

The author declares no conflict of interest.

Research involving human participants and/or animals

The article is a review article. Therefore, there is no human participants or animals.

Informed consent

The article is not a research article.

Additional information

Handling Editor: E. Agostinelli.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Soda, K. Spermine and gene methylation: a mechanism of lifespan extension induced by polyamine-rich diet. Amino Acids 52, 213–224 (2020). https://doi.org/10.1007/s00726-019-02733-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00726-019-02733-2

Keywords

Navigation