Reproductive investment often comes at a cost to longevity, but the mechanisms that underlie these long‐term effects are not well understood. In male vertebrates, elevated testosterone has been shown to increase reproductive success, but simultaneously to decrease survival. One factor that may contribute to or serve as a biomarker of these long‐term effects of testosterone on longevity is telomeres, which are often positively related to lifespan and have been shown to shorten in response to reproduction. In this longitudinal study, we measured the effects of experimentally elevated testosterone on telomere shortening in free‐living, male dark‐eyed juncos (
- Award ID(s):
- 1656194
- NSF-PAR ID:
- 10245275
- Date Published:
- Journal Name:
- Scientific Reports
- Volume:
- 11
- Issue:
- 1
- ISSN:
- 2045-2322
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Junco hyemalis carolinensis ), a system in which the experimental elevation of testosterone has previously been shown to increase reproductive success and reduce survival. We found a small, significant effect of testosterone treatment on telomeres, with testosterone‐treated males exhibiting significantly greater telomere shortening with age than controls. These results are consistent with the hypothesis that increased telomere shortening may be a long‐term cost of elevated testosterone exposure. As both testosterone and telomeres are conserved physiological mechanisms, our results suggest that their interaction may apply broadly to the long‐term costs of reproduction in male vertebrates. -
Abstract Actuarial senescence (called ‘senescence’ hereafter) often shows broad variation at the intraspecific level. Phenotypic plasticity likely plays a central role in among‐individual heterogeneity in senescence rate (i.e. the rate of increase in mortality with age), although our knowledge on this subject is still very fragmentary. Polyphenism—the unique sub‐type of phenotypic plasticity where several discrete phenotypes are produced by the same genotype—may provide excellent study systems to investigate if and how plasticity affects the rate of senescence in nature.
In this study, we investigated whether facultative paedomorphosis influences the rate of senescence in a salamander,
Ambystoma mavortium nebulosum . Facultative paedomorphosis, a unique form of polyphenism found in dozens of urodele species worldwide, leads to the production of two discrete, environmentally induced phenotypes: metamorphic and paedomorphic individuals. We leveraged an extensive set of capture–recapture data (8948 individuals, 24 years of monitoring) that were analysed using multistate capture–recapture models and Bayesian age‐dependent survival models.Multistate models revealed that paedomorphosis was the most common developmental pathway used by salamanders in our study system. Bayesian age‐dependent survival models then showed that paedomorphs have accelerated senescence in both sexes and shorter adult lifespan (in females only) compared to metamorphs. In paedomorphs, senescence rate and adult lifespan also varied among ponds and individuals. Females with good body condition and high lifetime reproductive success had slower senescence and longer lifespan. Late‐breeding females also lived longer but showed a senescence rate similar to that of early‐breeding females. Moreover, males with good condition had longer lifespan than males with poor body condition, although they had similar senescence rates. In addition, late‐breeding males lived longer but, unexpectedly, had higher senescence than early‐breeding males.
Overall, our work provides one of the few empirical cases suggesting that environmentally cued polyphenism could affect the senescence of a vertebrate in nature, thus providing insights on the ecological and evolutionary consequences of developmental plasticity on ageing.
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Abstract Building on the predictions of state‐dependent life‐history theory, telomeres are hypothesized to either correlate with or function as an adaptive, proximate mediator of an individual's behaviour and life‐history strategy. To further understand the relationship between telomeres, behaviour and life‐history strategies, we measured male behaviour, telomere lengths and telomere dynamics in a free‐living population of known‐age, male wire‐tailed manakins
Pipra filicauda .Male wire‐tailed manakins perform coordinated displays with other males at leks and these displays form the basis of long‐term coalition partnerships. Males exhibit consistent individual differences in the number of social partners within their social network and the frequency of social interactions. Male sociality is also positively correlated with both social rise and reproductive success.
We measured male behaviour using a telemetry‐based, proximity datalogging system and blood telomere lengths were quantified using qPCR. We examined the relationships between telomere length, telomere dynamics, social status, and male behaviour. We also quantified the repeatability of telomere lengths, examined age‐related changes in telomere length, and tested for instances of telomere elongation that exceed residual error in telomere length.
Telomere length was found to be highly repeatable. More social males exhibited shorter telomeres and higher rates of telomere attrition. Telomeres did not significantly vary with age within or between individuals in either of the male social classes. Two out of 25 individuals exhibited patterns telomere elongation that exceeded residual error in telomere measurements.
Here we show that telomeres consistently vary between male wire‐tailed manakins and these differences are related to variation in male social behaviour. In this relatively long‐lived species, telomeres appear to be flexible traits that can increase or decrease in length. Overall, this study provides observational support for the hypothesis that telomeres act as a molecular marker that relates to behaviour in a state‐dependent manner. We also provide insight into the molecular consequences of individual variation in male social behaviour.
A free
Plain Language Summary can be found within the Supporting Information of this article. -
Abstract The mechanisms that underlie senescence are not well understood in insects. Telomeres are conserved repetitive sequences at chromosome ends that protect DNA during replication. In many vertebrates, telomeres shorten during cell division and in response to stress and are often used as a cellular marker of senescence. However, little is known about telomere dynamics across the lifespan in invertebrates. We measured telomere length in larvae, prepupae, pupae, and adults of two species of solitary bees,
Osmia lignaria andMegachile rotundata . Contrary to our predictions, telomere length was longer in later developmental stages in bothO. lignaria andM. rotundata. Longer telomeres occurred after emergence from diapause, which is a physiological state with increased tolerance to stress. InO. lignaria , telomeres were longer in adults when they emerged following diapause. InM. rotundata , telomeres were longer in the pupal stage and subsequent adult stage, which occurs after prepupal diapause. In both species, telomere length did not change during the 8 months of diapause. Telomere length did not differ by mass similarly across species or sex. We also did not see a difference in telomere length after adultO. lignaria were exposed to a nutritional stress, nor did length change during their adult lifespan. Taken together, these results suggest that telomere dynamics in solitary bees differ from what is commonly reported in vertebrates and suggest that insect diapause may influence telomere dynamics. -
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