Kärkkäinen Tiia, Briga Michael, Laaksonen Toni, Stier Antoine
Department of Biology, University of Turku, Turku, Finland.
Mol Ecol. 2022 Dec;31(23):6339-6359. doi: 10.1111/mec.16155. Epub 2021 Sep 26.
Telomere length is increasingly used as a biomarker of long-term somatic state and future survival prospects. While most studies have overlooked this aspect, biological interpretations based on a given telomere length will benefit from considering the level of within-individual repeatability of telomere length through time. Therefore, we conducted a meta-analysis on 74 longitudinal studies in nonmammalian vertebrates, with the aim to establish the current pattern of within-individual repeatability in telomere length and to identify the methodological (e.g., qPCR/TRF) and biological factors (e.g., age class, phylogeny) that may affect it. While the median within-individual repeatability of telomere length was moderate to high (R = 0.55; 95% CI: 0.05-0.95; N = 82), marked heterogeneity between studies was evident. Measurement method affected the repeatability estimate strongly, with TRF-based studies exhibiting high repeatability (R = 0.80; 95% CI: 0.34-0.96; N = 25), while repeatability of qPCR-based studies was markedly lower and more variable (R = 0.46; 95% CI: 0.04-0.82; N = 57). While phylogeny explained some variance in repeatability, phylogenetic signal was not significant (λ = 0.32; 95% CI: 0.00-0.83). None of the biological factors investigated here significantly explained variation in the repeatability of telomere length, being potentially obscured by methodological differences. Our meta-analysis highlights the high variability in within-individual repeatability estimates between studies and the need to put more effort into separating technical and biological explanations. This is important to better understand to what extent biological factors can affect the repeatability of telomere length and thus the interpretation of telomere length data.
端粒长度越来越多地被用作长期体细胞状态和未来生存前景的生物标志物。虽然大多数研究都忽略了这一方面,但基于给定端粒长度的生物学解释将受益于考虑端粒长度随时间的个体内重复性水平。因此,我们对74项非哺乳动物脊椎动物的纵向研究进行了荟萃分析,目的是确定端粒长度个体内重复性的当前模式,并确定可能影响它的方法学(如qPCR/TRF)和生物学因素(如年龄组、系统发育)。虽然端粒长度的个体内重复性中位数为中等至高(R = 0.55;95% CI:0.05 - 0.95;N = 82),但研究之间存在明显的异质性。测量方法对重复性估计有很大影响,基于端粒限制性片段分析(TRF)的研究显示出高重复性(R = 0.80;95% CI:0.34 - 0.96;N = 25),而基于定量聚合酶链反应(qPCR)的研究的重复性明显较低且更具变异性(R = 0.46;95% CI:0.04 - 0.82;N = 57)。虽然系统发育解释了重复性的一些方差,但系统发育信号并不显著(λ = 0.32;95% CI:0.00 - 0.83)。这里研究的生物学因素均未显著解释端粒长度重复性的变化,可能被方法学差异所掩盖。我们的荟萃分析强调了研究之间个体内重复性估计的高度变异性,以及需要更加努力地区分技术和生物学解释。这对于更好地理解生物学因素在多大程度上可以影响端粒长度的重复性,从而影响端粒长度数据的解释非常重要。