Abstract

Telomere length is a marker of cellular senescence that relates to different components of individual fitness. Oxidative stress is often claimed as a main proximate factor contributing to telomere attrition, although the importance of this factor in vivo has recently been challenged. Early development represents an ideal scenario to address this hypothesis because it is characterized by the highest rates of telomere attrition of the life and by an arguably high susceptibility to oxidative stress. We tested the effect of oxidative stress on telomere dynamics during early development by exposing pied flycatcher nestlings (Ficedula hypoleuca) to either an oxidative challenge (diquat injections), an antioxidant (vitamin E) or control treatments (PBS injections and supplementation with vehicle substance). We found no effects of treatments on average telomere change during the nestling period. However, vitamin E supplementation, which increased growth, removed the association between initial telomere length and telomere attrition. Diquat-treated nestlings, by contrast, showed no differences in growth or telomere dynamics with respect to controls. These results do not support the hypothesis that oxidative stress is the main direct mechanism explaining telomere attrition in vivo, and highlight the importance of micronutrient intake during early development on telomere dynamics. Studies addressing alternative action pathways of vitamins on growth and telomere dynamics, perhaps via restoration mechanisms, would provide important insights on the proximate factors affecting telomere attrition during this critical phase of life.

Highlights

  • Telomeres are repetitive non-coding DNA sequences that protect the ends of eukaryotic chromosomes during cell replication (Blackburn, 1991)

  • We found a moderate effect of our treatments on nestling growth, characterized by an increase in body mass gain in V relative to C nestlings

  • Our initial hypothesis that oxidative stress would enhance telomere attrition during early development was not supported: neither D nor V nestlings differed from C chicks in telomere change from hatching to fledging

Read more

Summary

Introduction

Telomeres are repetitive non-coding DNA sequences that protect the ends of eukaryotic chromosomes during cell replication (Blackburn, 1991). Telomere shortening rates are high during early phases of development (e.g., Salomons et al, 2009; Heidinger et al, 2012), precisely in a Oxidative Stress, Telomeres and Development period of life when exposure to harsh conditions can have longlasting consequences on adult phenotype and fitness (Lindstrom, 1999). Telomere sequences are rich in guanine, a base that is sensitive to oxidative modifications that result in double and single-stranded breaks to DNA (Kawanishi and Oikawa, 2004). Such DNA damage impairs replication during cell division, leading to enhanced telomere attrition when oxidative stress levels increase

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call