Duplication of the mitochondrial control region is associated with increased longevity in birds

被引:24
|
作者
Skujina, Ilze [1 ]
McMahon, Robert [1 ]
Lenis, Vasileios Panagiotis E. [1 ]
Gkoutos, Georgios V. [1 ,2 ,3 ]
Hegarty, Matthew [1 ]
机构
[1] Aberystwyth Univ, IBERS, Aberystwyth SY23 3EE, Dyfed, Wales
[2] Univ Birmingham Edgbaston, Ctr Computat Biol, Inst Canc & Genom Sci, Haworth Bldg, Birmingham B15 2TT, W Midlands, England
[3] Univ Hosp Birmingham NHS Fdn Trust, Inst Translat Med, Birmingham B15 2TT, W Midlands, England
来源
AGING-US | 2016年 / 8卷 / 08期
基金
英国生物技术与生命科学研究理事会;
关键词
control region duplication; mitochondrial genome; birds; lifespan; comparative genomics; genetics; ageing; MOLECULAR EVOLUTION; METABOLIC-RATE; LIFE; GENOMES; RATES; SIZE;
D O I
10.18632/aging.101012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite a number of biochemical and lifestyle differences which should increase risk of oxidative damage to their mitochondrial DNA (mtDNA) and thus reduce expected lifespan, avian species often display longer lifespans than mammals of similar body mass. Recent work in mammalian ageing has demonstrated that functional mitochondrial copy number declines with age. We noted that several bird species display duplication of the control region (CR) of the mtDNA to form a pseudo-control region (YCR), apparently an avian-specific phenomenon. To investigate whether the presence of this duplication may play a similar role in longevity to mitochondrial copy number in mammals, we correlated body mass and longevity in 92 avian families and demonstrate a significant association. Furthermore, outlier analysis demonstrated a significant (p=0.01) difference associated with presence of the YCR duplication in longer-lived avian species. Further research is required to determine if the YCR does indeed alter mitochondrial function or resilience to oxidative damage, but these findings provide an intriguing hint of how mitochondrial sequences may be related to an extended lifespan.
引用
收藏
页码:1781 / 1789
页数:9
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