Université de Strasbourg, Institut Pluridisciplinaire Hubert Curien, Département Ecologie, Physiologie et Ethologie, Strasbourg, France ; Centre national de la recherche scientifique (CNRS), Strasbourg, France.
PLoS One. 2013 Dec 9;8(12):e81496. doi: 10.1371/journal.pone.0081496. eCollection 2013.
Telomeres are repetitive non coding DNA sequences located at the end of eukaryotic chromosomes, which maintain the integrity of the genome by hiding the chromosome ends from being recognised as double stranded breaks. Telomeres are emerging as biomarkers for ageing and survival, and are susceptible to reflect different individual life history trajectories. In particular, the telomere length with which one starts in life has been shown to be linked with individual life-long survival, suggesting that telomere dynamics can be a proxy for individual fitness and thereby be implicated in evolutionary trade-offs. As a consequence, an increasing number of studies were conducted on telomeres in the fields of ecology and evolutionary biology, in which telomere length was almost exclusively measured from blood samples. However, not only do the number of repeats of the telomeric sequences vary among species, but also within species with great inter-individual telomere lengths variability with age, tissues, and chromosomes. This raises the issue of the exact biological meaning of telomere measurement in blood cells and stimulated the study of the correlation of telomere lengths among tissues over age. By measuring telomere length in adult zebra finches (Taeniopygia guttata) in different somatic tissues displaying variable cell turnovers (bone marrow, brain, spleen, pectoral muscle, heart, liver and in red blood cells), we checked that the measure of telomere length in red blood cells is related to telomere lengths in the other tissues. Here we show significant relationships between the telomere lengths of red blood cells and several somatic tissues at adulthood. As red blood cells are easily accessible and suitable for the longitudinal monitoring of the individual rate of telomere loss, our study confirms that telomere length measured in red blood cells could serve as a surrogate for telomere length in the whole avian organism.
端粒是位于真核染色体末端的重复非编码 DNA 序列,通过将染色体末端隐藏起来,使其不被视为双链断裂,从而维持基因组的完整性。端粒作为衰老和存活的生物标志物正在出现,并且容易反映不同个体的生命史轨迹。特别是,一个人在生命开始时的端粒长度与个体终身存活有关,这表明端粒动力学可以作为个体适应度的代表,并因此涉及到进化权衡。因此,越来越多的研究在生态学和进化生物学领域中对端粒进行了研究,其中端粒长度几乎完全是从血液样本中测量的。然而,不仅端粒序列的重复次数在物种之间有所不同,而且在物种内,个体之间的端粒长度也存在很大的差异,随着年龄、组织和染色体的变化而变化。这就提出了在血细胞中测量端粒的确切生物学意义的问题,并刺激了研究随着年龄的增长,组织间端粒长度的相关性。通过测量不同体细胞组织(骨髓、大脑、脾脏、胸肌、心脏、肝脏和红细胞)中具有不同细胞周转率的成年斑马雀(Taeniopygia guttata)的端粒长度,我们检查了红细胞中端粒长度与其他组织中端粒长度的关系。在这里,我们显示了成年红细胞与几种体细胞组织之间的端粒长度存在显著关系。由于红细胞易于获取,并且适合于个体端粒丢失率的纵向监测,因此我们的研究证实,在红细胞中测量的端粒长度可以作为整个鸟类生物体内的端粒长度的替代物。