mtDNA
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An A to G point mutation
at position 3243 on the
Mitochondrial DNA
causes MELAS and MIDD.
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A-Z   A B C D E F G H I J K L M N O P Q R S T U V W X Y Z   A-Z

  Cybrid Cells

Cybrid Cells are used to investigate the effects of mtDNA mutations.

Firstly a cultured human cell has it's Mitochondria removed; then a cell from a heteroplasmic individual has it nucleus removed; finally these two cells are merged.

Suppose a heteroplasmic individual has a mutation load of 60%: The resulting Cybrid Cell will also have a mutation load of 60%.

This Cybrid Cell is then grown many times. As the Cybrid Cells divide, (Mitosis), the mitochondria are randomly divided between the two new cells. Thus, the daughter cells may have a higher or lower mutation load. If these cells are selected and grown, strains of Cybrid Cells can be grown which have higher or lower mutation loads.

Once this process of selection and re-growing has been repeated several times, batches of Cybrid Cells can be created which have average mutation loads of 70%, 80%, even 90% mutation load.

The behaviour of these cells can then be examined with constant Nuclear DNA input - the only difference being the heteroplasmic mutation load. 

See Also
mtDNA
Heteroplasmy
Mitochondria
Mitosis


Author: Andy Collinson. Although I don't have any medical qualifications, as a sufferer of Diabetes, Deafness and Tinnitus caused by the A3243G mtDNA defect, I do have a very keen interest in the subject.

Date Page Updated: 25 April 2005


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