
Paternal age and telomere length in twins: the germ stem cell selection paradigm
Author(s) -
Hjelmborg Jacob B.,
Dalgård Christine,
Mangino Massimo,
Spector Tim D.,
Halekoh Ulrich,
Möller Sören,
Kimura Masayuki,
Horvath Kent,
Kark Jeremy D.,
Christensen Kaare,
Kyvik Kirsten O.,
Aviv Abraham
Publication year - 2015
Publication title -
aging cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.103
H-Index - 140
eISSN - 1474-9726
pISSN - 1474-9718
DOI - 10.1111/acel.12334
Subject(s) - telomere , biology , epigenetics , genetics , germline , somatic cell , offspring , stem cell , dna methylation , trait , gene , pregnancy , gene expression , computer science , programming language
Summary Telomere length, a highly heritable trait, is longer in offspring of older fathers. This perplexing feature has been attributed to the longer telomeres in sperm of older men and it might be an ‘epigenetic’ mechanism through which paternal age plays a role in telomere length regulation in humans. Based on two independent (discovery and replication) twin studies, comprising 889 twin pairs, we show an increase in the resemblance of leukocyte telomere length between dizygotic twins of older fathers, which is not seen in monozygotic twins. This phenomenon might result from a paternal age‐dependent germ stem cell selection process, whereby the selected stem cells have longer telomeres, are more homogenous with respect to telomere length, and share resistance to aging.