Analysis of mitochondrial DNA in microfluidic systems.

Abnormalities in mitochondrial function play a major role in many human diseases. It is often of critical importance to ascertain what proportion of the mitochondria within a cell, or cells, bear a given mutation (the mitochondrial "demographics"). In this work, a rapid, novel, on-chip procedure was used, in which a restriction enzyme was employed to excise a mitochondrial DNA (mtDNA) sequence from plasmid DNA that acted as a prototypical mitochondrial genome. The DNA was then denatured, reassembled to form duplexes, fluorescently labelled and analysed. This method was able to differentiate between a homogeneous population and a heterogeneous population. Using a microfluidic chip, the method could be performed in about 45 min, even without robotics or multiplexed operation, whereas conventional methods of analysis require days to perform. This method may ultimately form the basis for a means of characterizing the mitochondrial demographics of a single cell.

[1]  C. Mawrin,et al.  Heterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disorders , 2001, Journal of medical genetics.

[2]  Igor L. Medintz,et al.  High-performance multiplex SNP analysis of three hemochromatosis-related mutations with capillary array electrophoresis microplates. , 2001, Genome research.

[3]  E. Shoubridge Nuclear genetic defects of oxidative phosphorylation. , 2001, Human molecular genetics.

[4]  R. Mathies,et al.  Polymorphism ratio sequencing: a new approach for single nucleotide polymorphism discovery and genotyping. , 2003, Genome research.

[5]  K. Kaler,et al.  An integrated method for mutation detection using on‐chip sample preparation, single‐stranded conformation polymorphism, and heteroduplex analysis , 2004, Electrophoresis.

[6]  W. Anderson,et al.  The frequency of heteroplasmy in the HVII region of mtDNA differs across tissue types and increases with age. , 2000, American journal of human genetics.

[7]  M. Woischnik,et al.  Pattern of organization of human mitochondrial pseudogenes in the nuclear genome. , 2002, Genome research.

[8]  E. Gross,et al.  A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC , 1999, Human Genetics.

[9]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[10]  J P Landers,et al.  Rapid detection of deletion, insertion, and substitution mutations via heteroduplex analysis using capillary- and microchip-based electrophoresis. , 2000, Genome research.

[11]  M. Somerville,et al.  Heteroduplex-based genotyping with microchip electrophoresis and dHPLC. , 2003, Genetic testing.

[12]  D. Wallace Mitochondrial diseases in man and mouse. , 1999, Science.

[13]  R. Mathies,et al.  Single-molecule detection of DNA separations in microfabricated capillary electrophoresis chips employing focused molecular streams. , 1999, Analytical chemistry.