» Articles » PMID: 27662635

Interactions Between Parental Traits, Environmental Harshness and Growth Rate in Determining Telomere Length in Wild Juvenile Salmon

Overview
Journal Mol Ecol
Date 2016 Sep 24
PMID 27662635
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

A larger body size confers many benefits, such as increased reproductive success, ability to evade predators and increased competitive ability and social status. However, individuals rarely maximize their growth rates, suggesting that this carries costs. One such cost could be faster attrition of the telomeres that cap the ends of eukaryotic chromosomes and play an important role in chromosome protection. A relatively short telomere length is indicative of poor biological state, including poorer tissue and organ performance, reduced potential longevity and increased disease susceptibility. Telomere loss during growth may also be accelerated by environmental factors, but these have rarely been subjected to experimental manipulation in the natural environment. Using a wild system involving experimental manipulations of juvenile Atlantic salmon Salmo salar in Scottish streams, we found that telomere length in juvenile fish was influenced by parental traits and by direct environmental effects. We found that faster-growing fish had shorter telomeres and there was a greater cost (in terms of reduced telomere length) if the growth occurred in a harsher environment. We also found a positive association between offspring telomere length and the growth history of their fathers (but not mothers), represented by the number of years fathers had spent at sea. This suggests that there may be long-term consequences of growth conditions and parental life history for individual longevity.

Citing Articles

Acclimation during Embryogenesis Remodulates Telomerase Activity and Gene Expression in Baikal Whitefish Larvae, Mitigating the Effects of Acute Temperature Stress.

Koroleva A, Vakhteeva E, Epifantsev A, Sukhanova L, Yakhnenko V, Glyzina O Animals (Basel). 2024; 14(19).

PMID: 39409788 PMC: 11476280. DOI: 10.3390/ani14192839.


Linking telomere dynamics to evolution, life history and environmental change: perspectives, predictions and problems.

Monaghan P Biogerontology. 2024; 25(2):301-311.

PMID: 38252370 PMC: 10998769. DOI: 10.1007/s10522-023-10081-8.


Sex and early-life conditions shape telomere dynamics in an ectotherm.

Hansson A, Wapstra E, While G, Olsson M J Exp Biol. 2024; 227(3).

PMID: 38230426 PMC: 10912812. DOI: 10.1242/jeb.246512.


Thermal Preconditioning Alters the Stability of Hump-Snout Whitefish () and Its Hybrid Form, Showing Potential for Aquaculture.

Sapozhnikova Y, Koroleva A, Yakhnenko V, Volkova A, Avezova T, Glyzina O Biology (Basel). 2023; 12(10).

PMID: 37887058 PMC: 10603914. DOI: 10.3390/biology12101348.


Does pre-spawning catch and release angling affect offspring telomere dynamics in Atlantic salmon?.

Duncan E, Papatheodoulou M, Metcalfe N, McLennan D Conserv Physiol. 2023; 11(1):coad018.

PMID: 37113976 PMC: 10129346. DOI: 10.1093/conphys/coad018.


References
1.
Blanckenhorn W . The evolution of body size: what keeps organisms small?. Q Rev Biol. 2000; 75(4):385-407. DOI: 10.1086/393620. View

2.
Metcalfe N, Monaghan P . Compensation for a bad start: grow now, pay later?. Trends Ecol Evol. 2001; 16(5):254-260. DOI: 10.1016/s0169-5347(01)02124-3. View

3.
Campisi J, Kim S, Lim C, Rubio M . Cellular senescence, cancer and aging: the telomere connection. Exp Gerontol. 2001; 36(10):1619-37. DOI: 10.1016/s0531-5565(01)00160-7. View

4.
Cawthon R . Telomere measurement by quantitative PCR. Nucleic Acids Res. 2002; 30(10):e47. PMC: 115301. DOI: 10.1093/nar/30.10.e47. View

5.
von Zglinicki T . Oxidative stress shortens telomeres. Trends Biochem Sci. 2002; 27(7):339-44. DOI: 10.1016/s0968-0004(02)02110-2. View