Skip to content
Open access · CC-BY via OpenAlex

Genome-Wide Association Study of Relative Telomere Length

Jennifer Prescott, Peter Kraft, Daniel I. Chasman, Sharon A. Savage, Lisa Mirabello, Sonja I. Berndt, Joel L. Weissfeld, Jiali Han, Richard B. Hayes, Stephen J. Chanock, David J. Hunter, Immaculata De Vivo

PLoS ONE · 2011 · ▲ 119 citations

Abstract

Telomere(definition) function is essential to maintaining the physical integrity of linear chromosomes and healthy human aging. The probability of forming proper telomere structures depends on the length of the telomeric DNA tract. We attempted to identify common genetic variants associated with log relative telomere length using genome-wide genotyping data on 3,554 individuals from the Nurses' Health Study and the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial that took part in the National Cancer Institute Cancer Genetic Markers of Susceptibility initiative for breast and prostate cancer. After genotyping 64 independent SNPs selected for replication in additional Nurses' Health Study and Women's Genome Health Study participants, we did not identify genome-wide significant loci; however, we replicated the inverse association of log relative telomere length with the minor allele variant [C] of rs16847897 at the TERC locus (per allele β = -0.03, P = 0.003) identified by a previous genome-wide association study. We did not find evidence for an association with variants at the OBFC1 locus or other loci reported to be associated with telomere length. With this sample size we had >80% power to detect β estimates as small as ±0.10 for SNPs with minor allele frequencies of ≥0.15 at genome-wide significance. However, power is greatly reduced for β estimates smaller than ±0.10, such as those for variants at the TERC locus. In general, common genetic variants associated with telomere length homeostasis have been difficult to detect. Potential biological and technical issues are discussed.

◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:

Read at source →

Provenance

Source
OpenAlex
DOI
10.1371/journal.pone.0019635
Canonical
link ↗
Fetched
2026-06-09 MST

Cite this

APA
Prescott, J., Kraft, P., Chasman, D.I., Savage, S.A., Mirabello, L., Berndt, S.I., Weissfeld, J.L., Han, J., Hayes, R.B., Chanock, S.J., Hunter, D.J., &amp; Vivo, I.D. (2011). Genome-Wide Association Study of Relative Telomere Length. <em>PLoS ONE</em>. https://doi.org/10.1371/journal.pone.0019635
Vancouver
Prescott J, Kraft P, Chasman DI, Savage SA, Mirabello L, Berndt SI, et al. Genome-Wide Association Study of Relative Telomere Length. PLoS ONE. 2011. doi:10.1371/journal.pone.0019635.
BibTeX
@article{jennifer2011Genome, title = {Genome-Wide Association Study of Relative Telomere Length}, author = {Jennifer Prescott and Peter Kraft and Daniel I. Chasman and Sharon A. Savage and Lisa Mirabello and Sonja I. Berndt and Joel L. Weissfeld and Jiali Han and Richard B. Hayes and Stephen J. Chanock and David J. Hunter and Immaculata De Vivo}, journal = {PLoS ONE}, year = {2011}, doi = {10.1371/journal.pone.0019635}, }

Research neighborhood

References, citing works, and semantically nearest findings. Click a node to open it.

Related findings