Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2018 Mar 5;373(1741):20160445.
doi: 10.1098/rstb.2016.0445.

The rate of telomere loss is related to maximum lifespan in birds

Affiliations
Comparative Study

The rate of telomere loss is related to maximum lifespan in birds

Gianna M Tricola et al. Philos Trans R Soc Lond B Biol Sci. .

Abstract

Telomeres are highly conserved regions of DNA that protect the ends of linear chromosomes. The loss of telomeres can signal an irreversible change to a cell's state, including cellular senescence. Senescent cells no longer divide and can damage nearby healthy cells, thus potentially placing them at the crossroads of cancer and ageing. While the epidemiology, cellular and molecular biology of telomeres are well studied, a newer field exploring telomere biology in the context of ecology and evolution is just emerging. With work to date focusing on how telomere shortening relates to individual mortality, less is known about how telomeres relate to ageing rates across species. Here, we investigated telomere length in cross-sectional samples from 19 bird species to determine how rates of telomere loss relate to interspecific variation in maximum lifespan. We found that bird species with longer lifespans lose fewer telomeric repeats each year compared with species with shorter lifespans. In addition, phylogenetic analysis revealed that the rate of telomere loss is evolutionarily conserved within bird families. This suggests that the physiological causes of telomere shortening, or the ability to maintain telomeres, are features that may be responsible for, or co-evolved with, different lifespans observed across species.This article is part of the theme issue 'Understanding diversity in telomere dynamics'.

Keywords: ageing; bird; comparative analysis; lifespan; senescence; telomeres.

PubMed Disclaimer

Conflict of interest statement

We have no competing interests.

Figures

Figure 1.
Figure 1.
Telomere length (from whole blood measured by TRF analysis) as a function of age in 19 bird species included in the comparative analysis. The lines are linear regressions, and the slope of the regression line for telomere length versus age was used as the telomere rate of change (TROC). The slope of the regression, its standard error and the r2 are printed within the panel of each species.
Figure 2.
Figure 2.
Maximum observed lifespan as a function of (a) telomere rate of change (TROC) and (b) mean telomere length in 19 bird species. (c) Mean telomere length plotted against TROC in 19 bird species. The dashed lines represent the regressions from the phylogenetic regressions without any other covariates included.
Figure 3.
Figure 3.
Trait evolution of telomere rate of change (TROC) mapped to the phylogeny in 19 bird species. Colours indicate different levels of the trait value (transformed values were used for mapping, but linear values are depicted for illustrative purposes in the legend). TROC shows a strong phylogenetic signal and the major families or clades of species which were included in this analysis show similar rates of telomere loss with age.

Similar articles

Cited by

References

    1. Haussmann MF, Treidel LA. 2015. Senescence: integrating biology from cradle to grave. In Integrative organismal biology (eds Martin LB, Ghalambor CK, Woods HA), pp. 1–19. Hoboken, NJ: Wiley Blackwell.
    1. Monaghan P, Charmantier A, Nussey DH, Ricklefs RE. 2008. The evolutionary ecology of senescence. Funct. Ecol. 22, 371–378. (10.1111/j.1365-2435.2008.01418.x) - DOI
    1. Baker DJ, Wijshake T, Tchkonia T, LeBrasseur NK, Childs BG, van de Sluis B, Kirkland JL, van Deursen JM. 2011. Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders. Nature 479, 232–236. (10.1038/nature10600) - DOI - PMC - PubMed
    1. Baker DJ, et al. 2016. Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan. Nature 530, 184–189. (10.1038/nature16932) - DOI - PMC - PubMed
    1. Coppé JP, Desprez PY, Krtolica A, Campisi J. 2010. The senescence-associated secretory phenotype: the dark side of tumor suppression. Annu. Rev. Pathol. 5, 99–118. (10.1146/annurev-pathol-121808-102144) - DOI - PMC - PubMed

Publication types