Fins as a reliable surrogate tissue for age-related changes of telomeres and DNA methylation in gonads of a short-lived fish.

IF 4.1 4区 医学 Q1 GERIATRICS & GERONTOLOGY
Milan Vrtílek, Anna Kromerová, Malahat Dianat, Miloslava Fojtová, Dagmar Čížková, Jiří Fajkus
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Abstract

Senescence is a multifactorial and individualised process of age-related physiological decline. Cellular markers, such as telomere length and DNA methylation, can reveal subtle changes associated with chronological age or expected lifespan. In this study, we evaluated the utility of fin tissue as a surrogate for assessing telomere length and proportion of DNA methylation in the gonads of a small, short-lived laboratory fish, the turquoise killifish (Nothobranchius furzeri). We collected fin and gonadal tissues from both females and males at three different ages. We extracted DNA to measure telomere length via terminal restriction fragment (TRF) analysis and global DNA methylation levels using double-digest restriction-associated DNA sequencing (ddRADseq). Our results show a notable correspondence between telomere length and DNA methylation patterns in fin and gonadal tissues. These findings support the use of fin biopsies as a non-lethal method for assessing ageing biomarkers in the gonads of small freshwater fish.

短寿鱼类性腺端粒和DNA甲基化随年龄变化的可靠替代组织鳍。
衰老是一个与年龄相关的生理衰退的多因素和个体化过程。细胞标志物,如端粒长度和DNA甲基化,可以揭示与实际年龄或预期寿命相关的细微变化。在这项研究中,我们评估了鳍组织作为一种小型、短寿实验鱼——绿松石鳉(Nothobranchius furzeri)生殖腺端粒长度和DNA甲基化比例的替代物的效用。我们收集了三个不同年龄的雌性和雄性的鳍和性腺组织。我们提取DNA,通过末端限制性内切片段(TRF)分析测量端粒长度,并使用双消化限制性内切相关DNA测序(ddRADseq)测量全球DNA甲基化水平。我们的研究结果显示端粒长度与鳍和性腺组织DNA甲基化模式之间存在显著的对应关系。这些发现支持使用鳍活组织检查作为一种非致死方法来评估小型淡水鱼性腺中老化的生物标志物。
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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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