mitochondrial dna analysis
TRANSCRIPT
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Mitochondrial DNA Analysis
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Lineage Markers
• Lineage markers are passed down from generation to generation without changing– Except for rare mutation events
• They can help determine the lineage (family tree) of an individual
• Y Chromosome Markers– Determine Paternal Lineage
• Mitochondrial Markers– Determine Maternal Lineage
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Maternal Inheritance of mtDNA
• Mitochondria are in cytoplasm – providing energy for the cell
• All cytoplasm comes from the egg or ovum• Sperm donates only nucleus to zygote• Therefore, all mitochondria are inherited
from mother only– No recombination– No paternal contribution
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Maternal Lineage
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Lineage Markers
• Great for genealogy or tracing evolution• However, the fact that these markers do
not recombine is a disadvantage for Forensics
• Cannot use the product rule when determine the probability of an ID match
• Cannot separate direct relatives apart:– mtDNA Profile could be anyone in family who
shares a maternal relative
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Why mtDNA?
• Although nuclear DNA is more powerful• mtDNA is more stable over time/conditions• Why is that?
– mtDNA is present in many copies– mtDNA exists within a double membrane
organelle• Can get more DNA – if sample is limited• Can get DNA from highly degraded source
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What is Mitochondria?
• Energy Power Plant of the Cell• Organelle – vital for Cellular Respiration• Many copies within one cell• Only organelle with it’s own DNA
– Many copies of mtDNA genome within one organelle
Circular mtDNA
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Mitochondrial DNA
• Contains 37 genes• Two main regions:
– Non-coding region – control’s mtDNA– Coding region – contains 37 genes
• Gene categories:– 22 tRNAs (translation RNA)– 2 rRNAs (ribosomal RNA – translation)– 13 genes used in cellular energy production
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Mitochondrial DNA
• Heavy vs. Light strands– Heavy greater number of guanines– Contains most of genes (28 out of 37)
• Tightly packed genome– No introns– Only 55 nucleotides not being used
• Two hypervariable regions– Within D-loop– HV1 and HV2
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mtDNA vs. Nuclear DNA
Nuclear• 3.2 Billion bps• 2 copies per cell• Linear• Inherited from father
and mother• Diploid genome• Recombination• Unique
mtDNA• 17,000 bps• Hundred’s copies• Circular• Inherited from mother
only• Haploid genome• No recombination• Shared by everyone
within maternal lineage
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http
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1 2 3 4 5 6 7 8 9 10 11 12
13 14 15 16 17 18 19 20 21 22 X Y
Human Genome 23 Pairs of Chromosomes + mtDNA
Sex-chromosomes
mtDNA
16,569 bp
Autosomes
Mitochondrial DNA
Nuclear DNA
3.2 billion bp
Located in cell nucleus
Located in mitochondria
(multiple copies in cell cytoplasm)
2 copies per cell
100s of copies per cell
Figure 2.3, J.M. Butler (2005) Forensic DNA Typing, 2nd Edition © 2005 Elsevier Academic Press
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Reference Sequence
• Human mtDNA has been entirely sequenced:– First in 1981 (Anderson et al)– Then confirmed in 1999 (Andrews et al)
• Cambridge Reference Sequence (CRS)• Now use the revised version (rCRS)• All other mtDNA is compared to the
reference sequence
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Differences from Nuclear DNA• mtDNA has different Genetic Code
– Which codons encode which amino acids– Small number of differences
• Fewer repair mechanisms– mtDNA has much higher mutation rate (10 X)
• Circular genome– Part of why mtDNA is more stable over time
• Increased number of genomes– 10’s of mito./cell and 100’s of genomes/mito.
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Applications of mtDNA
• Forensics of severely degraded samples• Medical studies of mitochondrial diseases• Evolutionary studies of humans• Genealogical studies• Real life examples:
– Tsar Nicholas II’s remains ID’d– Princess Anastasia proved to be false claim– Lacy Peterson’s body ID’d
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Genotyping mtDNA
First: • Used restriction enzymes to ID RFLP
differences• Began with 6 – eventually 12 enzymesNow • Sequence hypervariable regions and
examine sequence differences• Agreed upon regions are compared
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Hypervariable Regions
• D - loop or Control Region• Contains two regions with a lot of variation
among different individuals• These regions are amplified with PCR and
then sequenced• HV1 – 342 bps• HV2 – 268 bps • Profile is determined by differences in
sequence from the CRS
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Genotyping by Sequencing
• Rather than genotyping STRs or SNPs
• mtDNA profile is determined by sequencing both hypervariable regions
• mtDNA is a haploid genome
• Determining the mitochondria’s haplotype
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Screening Genotypes
• Before time is taken to sequence both regions entirely
• Many labs begin with a few screening genotypes first
• Screening:– Sequence specific oligo probes– Mini-sequencing– Cut with restriction enzymes– Others
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Clean Laboratory
• PCR is done with more cycles• mtDNA is already amplified due to multiple
copies per cell• Sample is already heavily degraded and
rare (otherwise wouldn’t be using mtDNA)• Therefore it is extra important that all
procedures are done in very clean lab• Limit or stop contamination
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Sequencing MethodsExtract mtDNA from sample (Q)
PCR and SequenceHV1 and HV2
Confirm Sequence
Note differences: Q from CRS
Extract mtDNA from reference (K)
PCR and SequenceHV1 and HV2
Confirm Sequence
Note differences: K from CRS
Compare Q and K sequences
Perform separatelyAnd after sample
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Sample Extraction• Typically dealing with materials with little
DNA:– Teeth, hair, dry bone, etc
• Sample is extremely degraded– Very fragile
• Must be handled with extreme caution• Usually tissue is ground up and then DNA
extracted via Organic Extraction• Also worry about PCR inhibitors
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Microscopic Comparisons of Hair
• Must be done before DNA is extracted• Hair (and fibers) can be compared under
microscope• Look for similarities between samples
– Color, shape, texture, internal components• May be able to identify whether hair is
from suspect, victim or someone unrelated to crime scene
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mtDNA Quantity
• mtDNA must be quantified just like nuclear DNA – before PCR can begin
• Use same methods as nuclear DNA:– Real time PCR– Blots, etc
• Some laboratories will quantify the amount of nuclear DNA and then use a rough formula to estimate amount of mtDNA that should be expected
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PCR Protocol for mtDNA
• Normal nuclear DNA PCR uses around 30 cycles
• mtDNA usually uses 34 to 40 cycles– Or even more!
• Excessive Taq Polymerase might be added
• More of PCR product may be used for sequence than normal protocols
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Sanger Sequencing Method
1977• Fredrick Sanger• Dideoxy sequencing• Dideoxys are nucleotides that contain no
free oxygen at all– These nucleotides cannot form chains– Polymerase stops copying DNA’s sequence
when it adds a dideoxy base – Make each nucleotide with dideoxy sugar
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Sanger Method
• Dideoxy nucleotides:
deoxyribose
OH
OH
HO-CH2
dideoxyribose
OH
OH
HO-CH2
ribose
OH
OH
HO-CH2
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Sanger Method
• In four tubes add:– DNA of unknown sequence– Everything necessary for DNA replication– One of each dideoxy nucleotide
• Each tube has a different dideoxy nucleotide in it (A, C, G or T)
• DNA polymerase will stop working once it adds a dideoxy base
• Therefore, get different lengths of copied DNA
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Sanger Method
• Run each separate tube in it’s own lane on a gel– “A” lane, the “T” lane, etc
• Important – some regular nucleotide is also added so that sequence can continue past some of the time
• Fragments of different lengths• Read the four lanes to determine sequence
of complete DNA fragment
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Sanger Method
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Modern Sequencing
• Added florescent dyes:– A is red– C is blue– T is green– G is yellow
• Now can run all four tubes in same lane• Automate entire process:
– Invented an automated sequencer and a computer program to read the gels
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Modern Sequencing
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Reading Sequence off Gel
• Determine the sequence from this gel:
dd-Add-Cdd-Tdd-G
TGCACTGAATCAGTGCTACGTGACTTAGTCACGA
Direct ReadActual Sequence
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Building sequences
• Based on overlapping fragments
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C – Stretches • String of cytosine’s in a row
– 8 to 14, or more• Exist in both hypervariable regions• Sequencing after the C-Stretch is very
difficult• Causes strand slippage for DNA
polymerase • Becomes “out of phase” between two
strands – sequences cannot be aligned• Need to re-sequence this region
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HV1 C-stretch
16189T
Poor quality sequence (two length variants out of phase)
Good quality sequence
Primer strategies typically used with C-stretch containing samples
(A)
(B)
(C)
C-stretch C-stretch
Use of internal primers Double reactions from the same strand
Figure 10.7, J.M. Butler (2005) Forensic DNA Typing, 2nd Edition © 2005 Elsevier Academic Press
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Mini-primers
• For highly degraded mtDNA use mini-primers just like for nuclear DNA
• Amplify small portions of the HV1 and HV2• Then sequence all pieces• Try to align to get entire sequence• This approach was used successfully to
recover a DNA profile from Neanderthal bones that were hundreds of thousands of years old
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Any Questions?
President’s Day MondayFinish mtDNA next class
Read Chapter 11
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Structure of mtDNAControl Region / D-Loop
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Controls
• Negative Control– Same master mix but with water or buffer– No DNA sample– Proves PCR reagents are not contaminated
• Positive Control– Master mix plus DNA of known concentration– Proves PCR reaction/conditions work
• Extraction Blanks– Controls for DNA extraction reagents/methods