TY - JOUR
T1 - Epigenetic inheritance of telomere length in wild birds
AU - Bauch, Christina
AU - Boonekamp, Jelle J
AU - Korsten, Peter
AU - Mulder, Ellis
AU - Verhulst, Simon
N1 - Funding Information:
CB was supported by a research fellowship of the German Research Foundation, DFG (grant no. BA 5422/1-1; www.dfg.de). JJB was funded by a grant of the Netherlands Organisation for Scientific Research, NWO (grant no. 823.01.009; www.nwo.nl) awarded to SV. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Martijn Salomons and the late Cor Dijkstra and all students involved in data and blood sample collection in the field, as well as Erica Zuidersma and Mike van het Land, who contributed to the laboratory analyses of TLs.
Funding Information:
Funding:CBwassupportedbyaresearch fellowshipoftheGermanResearchFoundation, DFG(grantno.BA5422/1-1;www.dfg.de).JJB wasfundedbyagrantoftheNetherlands OrganisationforScientificResearch,NWO(grant no. 823.01.009; www.nwo.nl) awarded to SV. The fundershadnoroleinstudydesign,datacollection andanalysis,decisiontopublish,orpreparationof themanuscript.
Publisher Copyright:
© 2019 Bauch et al. http://creativecommons.org/licenses/by/4.0/.
PY - 2019/2/14
Y1 - 2019/2/14
N2 - Telomere length (TL) predicts health and survival across taxa. Variation in TL between individuals is thought to be largely of genetic origin, but telomere inheritance is unusual, because zygotes already express a TL phenotype, the TL of the parental gametes. Offspring TL changes with paternal age in many species including humans, presumably through age-related TL changes in sperm, suggesting an epigenetic inheritance mechanism. However, present evidence is based on cross-sectional analyses, and age at reproduction is confounded with between-father variation in TL. Furthermore, the quantitative importance of epigenetic TL inheritance is unknown. Using longitudinal data of free-living jackdaws Corvus monedula, we show that erythrocyte TL of subsequent offspring decreases with parental age within individual fathers, but not mothers. By cross-fostering eggs, we confirmed the paternal age effect to be independent of paternal age dependent care. Epigenetic inheritance accounted for a minimum of 34% of the variance in offspring TL that was explained by paternal TL. This is a minimum estimate, because it ignores the epigenetic component in paternal TL variation and sperm TL heterogeneity within ejaculates. Our results indicate an important epigenetic component in the heritability of TL with potential consequences for offspring fitness prospects.
AB - Telomere length (TL) predicts health and survival across taxa. Variation in TL between individuals is thought to be largely of genetic origin, but telomere inheritance is unusual, because zygotes already express a TL phenotype, the TL of the parental gametes. Offspring TL changes with paternal age in many species including humans, presumably through age-related TL changes in sperm, suggesting an epigenetic inheritance mechanism. However, present evidence is based on cross-sectional analyses, and age at reproduction is confounded with between-father variation in TL. Furthermore, the quantitative importance of epigenetic TL inheritance is unknown. Using longitudinal data of free-living jackdaws Corvus monedula, we show that erythrocyte TL of subsequent offspring decreases with parental age within individual fathers, but not mothers. By cross-fostering eggs, we confirmed the paternal age effect to be independent of paternal age dependent care. Epigenetic inheritance accounted for a minimum of 34% of the variance in offspring TL that was explained by paternal TL. This is a minimum estimate, because it ignores the epigenetic component in paternal TL variation and sperm TL heterogeneity within ejaculates. Our results indicate an important epigenetic component in the heritability of TL with potential consequences for offspring fitness prospects.
UR - http://www.scopus.com/inward/record.url?scp=85061606252&partnerID=8YFLogxK
U2 - 10.1101/284208
DO - 10.1101/284208
M3 - Article
SN - 1553-7390
VL - 15
JO - PLoS Genetics
JF - PLoS Genetics
IS - 2
M1 - e1007827
ER -