Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations.

作者: Huanzheng Li , Jesse Slone , Lin Fei , Taosheng Huang

DOI: 10.3390/CELLS8060608

关键词:

摘要: The mitochondrion is the only organelle in the human cell, besides the nucleus, with its own DNA (mtDNA). Since the mitochondrion is critical to the energy metabolism of the eukaryotic cell, it should be unsurprising, then, that a primary driver of cellular aging and related diseases is mtDNA instability over the life of an individual. The mutation rate of mammalian mtDNA is significantly higher than the mutation rate observed for nuclear DNA, due to the poor fidelity of DNA polymerase and the ROS-saturated environment present within the …

参考文章(105)
Bing-Feng Zhang, Lei Xing, Peng-Fei Cui, Feng-Zhen Wang, Rong-Lin Xie, Jia-Liang Zhang, Mei Zhang, Yu-Jing He, Jin-Yuan Lyu, Jian-Bin Qiao, Bao-An Chen, Hu-Lin Jiang, Mitochondria apoptosis pathway synergistically activated by hierarchical targeted nanoparticles co-delivering siRNA and lonidamine. Biomaterials. ,vol. 61, pp. 178- 189 ,(2015) , 10.1016/J.BIOMATERIALS.2015.05.027
Sarah Myhill, John McLaren-Howard, Norman E. Booth, Chronic fatigue syndrome and mitochondrial dysfunction International Journal of Clinical and Experimental Medicine. ,vol. 2, pp. 1- 16 ,(2009)
Krisztian Stadler, Ira J. Goldberg, Katalin Susztak, The Evolving Understanding of the Contribution of Lipid Metabolism to Diabetic Kidney Disease Current Diabetes Reports. ,vol. 15, pp. 40- 40 ,(2015) , 10.1007/S11892-015-0611-8
Richard M. Andrews, Iwona Kubacka, Patrick F. Chinnery, Robert N. Lightowlers, Douglass M. Turnbull, Neil Howell, Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA Nature Genetics. ,vol. 23, pp. 147- 147 ,(1999) , 10.1038/13779
Gregory J Tranah, Michael A Nalls, Shana M Katzman, Jennifer S Yokoyama, Ernest T Lam, Yiqiang Zhao, Sean Mooney, Fridtjof Thomas, Anne B Newman, Yongmei Liu, Steven R Cummings, Tamara B Harris, Kristine Yaffe, None, Mitochondrial DNA Sequence Variation Associated with Dementia and Cognitive Function in the Elderly Journal of Alzheimer's Disease. ,vol. 32, pp. 357- 372 ,(2012) , 10.3233/JAD-2012-120466
K E Bendall, B C Sykes, Length heteroplasmy in the first hypervariable segment of the human mtDNA control region American Journal of Human Genetics. ,vol. 57, pp. 248- 256 ,(1995)
Aleksandra Maruszak, Krzysztof Safranow, Wojciech Branicki, Katarzyna Gawęda-Walerych, Ewelina Pośpiech, Tomasz Gabryelewicz, Jeffrey A. Canter, Maria Barcikowska, Cezary Żekanowski, The impact of mitochondrial and nuclear DNA variants on late-onset Alzheimer's disease risk. Journal of Alzheimer's Disease. ,vol. 27, pp. 197- 210 ,(2011) , 10.3233/JAD-2011-110710
Jeong-A Lim, Lishu Li, Or Kakhlon, Rachel Myerowitz, Nina Raben, Defects in calcium homeostasis and mitochondria can be reversed in Pompe disease Autophagy. ,vol. 11, pp. 385- 402 ,(2015) , 10.1080/15548627.2015.1009779
Tohru Kitada, Shuichi Asakawa, Nobutaka Hattori, Hiroto Matsumine, Yasuhiro Yamamura, Shinsei Minoshima, Masayuki Yokochi, Yoshikuni Mizuno, Nobuyoshi Shimizu, Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism Nature. ,vol. 392, pp. 605- 608 ,(1998) , 10.1038/33416
Mohammad Mehdi Banoei, Massoud Houshmand, Mehdi Shafa Shariat Panahi, Parvin Shariati, Maryam Rostami, Masoumeh Dehghan Manshadi, Tayebeh Majidizadeh, Huntington’s Disease and Mitochondrial DNA Deletions: Event or Regular Mechanism for Mutant Huntingtin Protein and CAG Repeats Expansion?! Cellular and Molecular Neurobiology. ,vol. 27, pp. 867- 875 ,(2007) , 10.1007/S10571-007-9206-5