Download Biology 445K Winter 2007 DNA Fingerprinting • For Friday 3/9 lab: in

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Medical genetics wikipedia , lookup

Mitochondrial DNA wikipedia , lookup

Mutagen wikipedia , lookup

Transposable element wikipedia , lookup

Quantitative trait locus wikipedia , lookup

Genome evolution wikipedia , lookup

Nutriepigenomics wikipedia , lookup

Primary transcript wikipedia , lookup

DNA paternity testing wikipedia , lookup

Human genome wikipedia , lookup

Genetic engineering wikipedia , lookup

DNA polymerase wikipedia , lookup

Molecular Inversion Probe wikipedia , lookup

Comparative genomic hybridization wikipedia , lookup

Zinc finger nuclease wikipedia , lookup

Cancer epigenetics wikipedia , lookup

Replisome wikipedia , lookup

Nucleosome wikipedia , lookup

Gene wikipedia , lookup

DNA damage theory of aging wikipedia , lookup

DNA vaccination wikipedia , lookup

Genetic drift wikipedia , lookup

Point mutation wikipedia , lookup

Designer baby wikipedia , lookup

Gel electrophoresis of nucleic acids wikipedia , lookup

Genomic library wikipedia , lookup

Vectors in gene therapy wikipedia , lookup

No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing wikipedia , lookup

DNA profiling wikipedia , lookup

Genomics wikipedia , lookup

Molecular cloning wikipedia , lookup

Hardy–Weinberg principle wikipedia , lookup

Population genetics wikipedia , lookup

Genome editing wikipedia , lookup

Epigenomics wikipedia , lookup

Extrachromosomal DNA wikipedia , lookup

United Kingdom National DNA Database wikipedia , lookup

Non-coding DNA wikipedia , lookup

DNA supercoil wikipedia , lookup

Therapeutic gene modulation wikipedia , lookup

Nucleic acid double helix wikipedia , lookup

Genealogical DNA test wikipedia , lookup

Nucleic acid analogue wikipedia , lookup

Site-specific recombinase technology wikipedia , lookup

Dominance (genetics) wikipedia , lookup

History of genetic engineering wikipedia , lookup

Cre-Lox recombination wikipedia , lookup

Bisulfite sequencing wikipedia , lookup

Deoxyribozyme wikipedia , lookup

Cell-free fetal DNA wikipedia , lookup

SNP genotyping wikipedia , lookup

Helitron (biology) wikipedia , lookup

Artificial gene synthesis wikipedia , lookup

Microevolution wikipedia , lookup

Microsatellite wikipedia , lookup

Transcript
Biology 445K
Winter 2007
DNA Fingerprinting
• For Friday 3/9 lab: in your lab notebook write out (in bullet style
NOT paragraph style) the steps for BOTH the check cell DNA
prep and the hair follicle DNA prep (pgs 4&5). EACH student
will do both preps. Photocopy notebook pages and turn in to CT
at beginning of lab. For each prep you will be using 400µ l of
extraction buffer.
• Read about PCR, DNA fingerprinting and Hardy-Weinberg in your
genetics text.
• Work the problems 1-5 before Wednesday March 12. Put in lab
notebook AND hand in photocopy
• A handout describing the PCR portion of this experiment will be
distributed on FRIDAY
Go to this link to see a PCR animation:
http://vector.cshl.org/resources/BiologyAnimationLibrary.htm
Choosing primers:
http://ls126.molsci.org/PCR_top.html
Links to the above sites as well as to DNA fingerprinting sites are posted on the
Biol 445K web site
DNA FINGERPRINTING WITH PCR uses PCR to analyze highly variable
microsatellite or minisatellite [aka VNTR (variable numbers of tandem repeats)]
loci to determine DNA identity (as in forensic blood tests) or to determine
parentage of an individual. Minisatellite sites are highly polymorphic* regions of
the genome that consist of repeated sequences. The repeat size is usually 10-60
base pairs long and the number of repeats varies from less than ten to several
dozen. These sites, which are scattered throughout the genome, are usually
“anonymous” markers in the sense that the repeat number does not affect the
phenotype of the individual and isn’t associated with the functioning of a gene.
*Recall that a polymorphic locus is typically defined as any gene or locus (site on
a chromosome) that has more than one variation present within a population. This
definition is of limited usefulness because at high levels of resolution (i.e. looking
1
at the DNA level at a very large number of individuals) most genes or loci will fit
this definition. So, generally speaking, a gene or locus is polymorphic if the rarer
allele(s) is (are) not too rare -- not less than 1% of the total copies in the
population.
Using DNA fingerprinting to exclude vs. to prove:
 Excluding identity: one set of mismatched genetic markers is sufficient
 Proving identity or proving parentage is another matter: the experimenter must
examine a number of highly polymorphic loci in the genome and do probability
calculations to estimate the likelihood of random matches (involves important
concepts in population genetics relating to allele frequencies).
D1S80 VNTR locus: The VNTR (minisatellite) locus D1S80 is located on the
distal portion of the short arm of chromosome 1. This site is highly polymorphic
with respect to the number of 16 base pair (bp) repeat units present between the
priming sites. This locus has been used in population genetic studies, identification
of extensively burned fire victims, identification of human remains and other
forensic studies.
#1 5’ GAAACTGGCCTCCAAACACTGCCCGCCG 3’
#2 5’ GTCTTGTTGGAGATGCACGTGCCCCTTGC 3’
The PCR bands generated with these primers represent codominant allelic
products that typically range from ~300 bp’s to ~800 bp’s, depending on the
number of 16-bp repeat units. In accordance with standard protocol the “shortest”
allele is designated allele 1 (with 18 repeats) and each allele containing an
additional repeat is designated as 2, 3, 4, etc.
Examine the table shown on the next page. Note that 13 different alleles of
this site were present in a sample of 94 Caucasians from the United States. A total
of 28 alleles of this site have been observed, so this table is incomplete.
2
The D1S80 repeat unit is 16 base pairs (bp) in length and alleles range
from approximately 350 to 1,000 bp.
3
 PCR Template preparation:
Each student will prep DNA from a hair follicle and from cheek cells.
4
Work the problems 1-5 before Wednesday March 12 TO HAND IN at
beginning of class.
1. Refer to your genetics text. How many different genotypes are possible for a
locus with 13 alleles? What is the general formula used for this calculation?
2. How many different heterozygous genotypes are possible at this locus?
5
Populations genetics and frequency estimations:
There are two reasons a pair of DNA profiles (examining multiple VNTR sites)
would match:
• the profiles came from the same individual
• the profiles came from two different individuals who share the same alleles at
all VNTR sites tested.
To address the latter possibility, a conservative statistical estimate is made as to
how frequently the DNA profile in question might occur in a given population.
3. Consider a match between two profiles in which only the D1S80 site was
examined. One DNA sample was from a forensic specimen (ie. blood or semen).
The other was from an individual accused of the crime. If the forensic specimen
was homozygous for allele 1, what is the chance that an individual picked at
random from the population would be of the same genotype? if the specimen was
heterozygous for alleles 13 and 11? [Assume the U.S. population meets the
conditions of the Hardy-Weinberg equilibrium]
4. VNTR loci tested in DNA fingerprinting are on different chromosomes and so
therefore show independent assortment. Consider estimates that incorporate data
6
from more than one polymorphic site. After the individual frequencies for each
VNTR gene pair are calculated, they can be multipled together. In other words, the
product rule of probability can be used to determine that likelihood of chance
match when more than one site is examined. Fill in the table below:
Calculating a DNA profile frequency
Allele frequency
Locus
band 1/band 2
1
0.08/0.02
2
0.15/0.04
3
0.08/0.06
4
0.22/0.09
Frequency of
genotype (HW)
Combined
frequency
-----
5. The cycling conditions for your PCR reactions are as follows.
Step
Time
Temperature
1
10 min.
94oC
2
1 min.
94oC
3
1 min.
65oC
4
1 min.
72oC
Repeat 2-4 35 more
5
times
6
7
10 min
Hold
15oC
4o C
a. For each step, briefly indicate what is occurring in the reaction at each step.
b. What is the theoretical amplification achieved in this reaction?
c. The annealing temperature typically depends on the stability of the templateprimer hybrid. What parameters would affect this stability?
d. What is a primer dimer?
7