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MITOCHONDRIAL GENOME

Abdul Jaleel K

Department of Zoology

Government College Kasaragod

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  • Mitochondrial DNA is a double stranded circular molecule, which is inherited from the mother in all multi-cellular organisms, though some recent evidence suggests that in rare instances mitochondria may also be inherited via a paternal route.

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  • There are about 2 to 10 transcripts of the mt-DNA in each mitochondrion.
  • Compared to chromosomes, it is relatively smaller, and contains the genes in a limited number.

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  • The size of mitochondrial genomes varies greatly among different organisms, with the largest found among plants, including that of the plant Arabidopsis, with a genome of 200 kbp in size and 57 protein-encoding genes.
  • The smallest mtDNA genomes include that of the protist Plasmodium falciparum, which has a genome of only 6 kbp and just 2 protein- encoding genomes.
  • Humans and other animals have a mitochondrial genome size of 17 kbp and 13 protein genes.

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  • Mitochondrial DNA consists of 5-10 rings of DNA and appears to carry 16,569 base pairs with 37 genes (13 proteins, 22 t-RNAs and two r-RNA) which are concerned with the pro­duction of proteins involved in respiration.
  • Out of the 37 genes, 13 are responsible for mak­ing enzymes, involved in oxidative phosphorylation, a process that uses oxygen and sugar to produce adenosine tri-phosphate .
  • The other 14 genes are responsible for making molecules, called transfer RNA (t-RNA) and ribosomal RNA (r-RNA).
  • In some metazoans, there are about 100 – 10,000 separate copies of mt-DNA present in each cell.

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  • Unlike nuclear DNA, mitochondrial DNA doesn’t get shuffled every generation, so it is presumed to change at a slower rate, which is useful for the study of human evolution.
  • Mito­chondrial DNA is also used in forensic science as a tool for identifying corpses or body parts and has been implicated in a number of genetic diseases, such as Alzheimer’s disease and diabetes.
  • Changes in mt-DNA can cause maternally inherited diseases, which leads to faster aging process and genetic disorders.

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  • Mitochondria convert the potential energy of food molecules into ATP by the Krebs cy­cle, electron transport and oxidative phosphorylation in presence of oxygen.
  • The energy from food molecules (e.g., glucose) is used to produce NADH and FADH2 molecules, via glycolysis and the Krebs cycle.
  • The protein complexes in the inner membrane (NADH de­hydrogenase, cytochrome c reductase, cytochrome c oxidase) use the released energy to pump protons (FT) against a gradient.

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