New Research In
Physical Sciences
Social Sciences
Featured Portals
Articles by Topic
Biological Sciences
Featured Portals
Articles by Topic
- Agricultural Sciences
- Anthropology
- Applied Biological Sciences
- Biochemistry
- Biophysics and Computational Biology
- Cell Biology
- Developmental Biology
- Ecology
- Environmental Sciences
- Evolution
- Genetics
- Immunology and Inflammation
- Medical Sciences
- Microbiology
- Neuroscience
- Pharmacology
- Physiology
- Plant Biology
- Population Biology
- Psychological and Cognitive Sciences
- Sustainability Science
- Systems Biology
Delayed paternal age of reproduction in humans is associated with longer telomeres across two generations of descendants
Edited* by Peter T. Ellison, Harvard University, Cambridge, MA, and approved May 11, 2012 (received for review February 7, 2012)

Abstract
Telomeres are repeating DNA sequences at the ends of chromosomes that protect and buffer genes from nucleotide loss as cells divide. Telomere length (TL) shortens with age in most proliferating tissues, limiting cell division and thereby contributing to senescence. However, TL increases with age in sperm, and, correspondingly, offspring of older fathers inherit longer telomeres. Using data and samples from a longitudinal study from the Philippines, we first replicate the finding that paternal age at birth is associated with longer TL in offspring (n = 2,023, P = 1.84 × 10−6). We then show that this association of paternal age with offspring TL is cumulative across multiple generations: in this sample, grandchildren of older paternal grandfathers at the birth of fathers have longer telomeres (n = 234, P = 0.038), independent of, and additive to, the association of their father’s age at birth with TL. The lengthening of telomeres predicted by each year that the father’s or grandfather’s reproduction are delayed is equal to the yearly shortening of TL seen in middle-age to elderly women in this sample, pointing to potentially important impacts on health and the pace of senescent decline in tissues and systems that are cell-replication dependent. This finding suggests a mechanism by which humans could extend late-life function as average age at reproduction is delayed within a lineage.
Footnotes
- ↵1To whom correspondence should be addressed. E-mail: dtae{at}dtae.net.
↵2M.G.H. and C.W.K. contributed equally to this work.
Author contributions: D.T.A.E., M.G.H., and C.W.K. designed research; D.T.A.E. performed research; D.T.A.E. analyzed data; and D.T.A.E., M.G.H., and C.W.K. wrote the paper.
The authors declare no conflict of interest.
↵*This Direct Submission article had a prearranged editor.
Citation Manager Formats
More Articles of This Classification
Social Sciences
Anthropology
Biological Sciences
Related Content
- No related articles found.
Cited by...
- Experimental demonstration that offspring fathered by old males have shorter telomeres and reduced lifespans
- The mitochondrial genome, paternal age and telomere length in humans
- The paternal age at conception effect on offspring telomere length: mechanistic, comparative and adaptive perspectives
- Older fathers' children have lower evolutionary fitness across four centuries and in four populations
- Spermatozoa telomeres determine telomere length in early embryos and offspring
- Telomere dynamics may link stress exposure and ageing across generations
- Reduced fitness in progeny from old parents in a natural population
- Telomerase Activity and Telomere Length in Male Germ Cells
- Cell biology of disease: Telomeropathies: An emerging spectrum disorder
- Age, the environment and our reproductive future: bonking baby boomers and the future of sex
- Adult Glucocorticoid Exposure Leads to Transcriptional and DNA Methylation Changes in Nuclear Steroid Receptors in the Hippocampus and Kidney of Mouse Male Offspring
- How "Reversible" Is Telomeric Aging?














