- Course Introduction
- 01: Evidence & DNA
- 02: Forensic Biology
- 03: DNA Extraction & Quantitation
- 04: DNA Amplification
- 05: Amplified DNA Product Separation
- 06: STR Data Analysis & Interpretation
- 07: Population Genetics & Statistics
- 08: Communicating Results
- 09: Other DNA Markers & Technologies
- Course Resources
- Laboratory Training Manual
President's DNA Initiative
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Advancing Justice Through DNA Technology
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Advancing Justice Through DNA Technology
DNA Analyst Training
mtDNA Sequencing
Home > Other DNA Markers & Technologies > Non-Nuclear DNA Markers > Mitochondrial DNA > mtDNA Sequencing
mtDNA sequencing technology is routinely used by a limited number of forensic laboratories worldwide because direct sequencing is time-consuming and labor-intensive.
Direct sequencing determines the order of bases along the template DNA. Automated fluorescent sequence technology has significantly increased the throughput of sequence information in the scientific communities. Often small quantity and degraded DNA are the only samples available in mtDNA forensic casework. The DNA is amplified and directly sequenced using the Sanger method.
The amplified product is:27, 30
- Digested with SAP-EXO I (shrimp alkaline phosphatase and exonuclease I) to remove excess deoxynucleotide triphosphate (dNTPs) and PCR primers
- Exposed to a sequencing primer and incorporation of dideoxyribonucleotide triphosphate (ddNTPs) for the sequencing reaction
- Denatured
- Separated by electrophoresis
Each ddNTP is labeled with a different fluorescent dye. Once the ddNTP is incorporated, chain elongation is terminated. The sequencing primers direct the sequencing of the forward or reverse reaction for each of the DNA strands. Interpretation of the data can be laborious, even with sophisticated software programs.
The amplification and sequencing primer sets are not available commercially in kits similar to the STR PCR amplification kits; however, these primers are published and can be ordered through commercial vendors.31, 32 Highly degraded DNA may not amplify efficiently with the primer sets for HV1 and HV2. Mini-primer sets have been developed to amplify smaller portions of HV1 and HV2 and have been successful in overcoming failure to amplify with the larger primers.33
Computer software programs, such as Sequencher™ (Gene Codes) are available to aid the analyst in the tedious task of data analysis.
Sequencher™ is a sequence analysis software program that:
- Builds projects for each sample
- Removes any sequence data of the primers
- Removes poor sequence data based on signal and spacing
- Produces complementary data of the reverse sequence reactions
- Aligns forward and reverse sequencing reactions
- Compares the sequence to the rCRS
A forensic DNA analyst independently examines, interprets and edits sequencing results prior to reporting.
