Mitochondrial Membranes and Mitochondrial Genome: Interactions and Clinical Syndromes

被引:2
|
作者
Almannai, Mohammed [1 ]
Salah, Azza [2 ]
El-Hattab, Ayman W. [2 ,3 ,4 ]
机构
[1] King Abdullah Specialized Children Hosp, Genet & Precis Med Dept, POB 22490, Riyadh, Saudi Arabia
[2] Univ Hosp Sharjah, Dept Pediat, POB 72772, Sharjah, U Arab Emirates
[3] Univ Sharjah, Dept Clin Sci, Coll Med, POB 72772, Sharjah, U Arab Emirates
[4] Kids Heart Med Ctr, Genet & Metab Dept, POB 505193, Abu Dhabi, U Arab Emirates
关键词
mitochondria; IMM; OMM; fission; fusion; mtDNA; ADENINE-NUCLEOTIDE TRANSLOCATOR; RECURRENT DE-NOVO; OPTIC ATROPHY; MTDNA STABILITY; DNA INSTABILITY; BARTH SYNDROME; MPV17; ENCODES; SLC25; FAMILY; COPY NUMBER; PROTEIN;
D O I
10.3390/membranes12060625
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are surrounded by two membranes; the outer mitochondrial membrane and the inner mitochondrial membrane. They are unique organelles since they have their own DNA, the mitochondrial DNA (mtDNA), which is replicated continuously. Mitochondrial membranes have direct interaction with mtDNA and are therefore involved in organization of the mitochondrial genome. They also play essential roles in mitochondrial dynamics and the supply of nucleotides for mtDNA synthesis. In this review, we will discuss how the mitochondrial membranes interact with mtDNA and how this interaction is essential for mtDNA maintenance. We will review different mtDNA maintenance disorders that result from defects in this crucial interaction. Finally, we will review therapeutic approaches relevant to defects in mitochondrial membranes.
引用
收藏
页数:15
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