Recombinant DNA Technology - Michigan Medicine · Recombinant DNA Technology Stephen B. Gruber, MD,...
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Recombinant DNA Technology
Stephen B. Gruber, MD, PhD
Division of Molecular Medicine and Genetics
November 4, 2002
Learning Objectives
• Know the basics of gene structure, function and regulation.
• Be familiar with the basic methods of molecular genetics.
• Understand the meaning of DNA sequence and amino acidpolymorphisms.
• Know how DNA sequence analysis is performed and befamiliar with methods of screening for differences.
• Have a general understanding of methods for gene transferinto tissue culture cells and the power of transgenictechnologies.
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Learning Objectives (1)
• Know the basics of gene structure, function and regulation.
• Be familiar with the basic methods of molecular genetics.
• Understand the meaning of DNA sequence and amino acidpolymorphisms.
• Know how DNA sequence analysis is performed and befamiliar with methods of screening for differences.
• Have a general understanding of methods for gene transferinto tissue culture cells and the power of transgenictechnologies.
Chromosomes, DNA, and Genes
CellNucleus
Chromosomes
Gene
Protein
Adapted from Understanding Gene Testing, NIH, 1995
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Genetic Code
A codon is made of 3 base pairs
64 codons total
1 codon (AUG) encodesmethionine and starts
translation of all proteins
3 codons stopprotein
translation
61 codons encode 20amino acids
(redundant code)
U A A
A U G
Met
G C A
Ala
DNA Transcription andTranslation
mRNA
Ribosome
Growingchain of
amino acids
Protein
Nuclearmembrane Cell membrane
DNA
Adapted from Understanding Gene Testing, NIH, 1995
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5' end
Promoter
RNA transcriptionstart site
3' end
Gene Structure
Stop site
Intron Exon 2 IntronExon 1 Exon 3
Splice sites
Exon 2Exon 1 Exon 3
mRNA
RNA Processing
Translation
Protein
DNA
PrimarymRNA
MaturemRNA
Processing
Transcription
Exon Intron Exon Intron Exon
GU AG
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Learning Objectives (2)
• Know the basics of gene structure, function and regulation.
• Be familiar with the basic methods of molecular genetics.– nucleic acid hybridization– Southern (DNA) and northern (RNA) blotting– PCR– DNA sequencing– basic steps involved in constructing & screening a cDNA library
• Understand the meaning of DNA sequence and amino acidpolymorphisms.
• DNA sequence analysis
• Transgenic technologies
from Textbook: 5.4
1944DNA is the
genetic material
1949Abnl Hemoglobin
in sickle cell anemia
1953Double helix
1956Glu 6 Val insickle hemoglobin
1966Completion of the
genetic code
1970First restriction
enzyme
1972Recombinant
plasmids
1975Southernblotting
1981Transgenic mice
1983Huntington
Disease genemapped
1985PCR
1986Positional cloning
(CGD, musculardystrophy,
retinoblastoma
1945 1950 1955 1960 1965 1970 1975 1980 1985 1990 1995 2000
1987Knockout
mice
1989Positional cloningwithout deletion (CF)
1990First NIH-approvedgene therapyexperiment
1996Complete yeastgenome sequence
19951st completebacterialgenome sequence
2001Draft human
genome sequence
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Preparing DNA for Analysis
Blood sample Centrifuge andextract DNA fromwhite blood cells
DNA for analysis
SINGLE-STRANDEDDNA PROBESFOR GENE A
MIXTURE OF SINGLE-STRANDEDDNA MOLECULES
+ B
B B
A
A
C
CC
D
D
D
E
EE
F
F F
ONLY A FORMS A STABLEDOUBLE-STRANDED COMPLEXES
A, C, E ALL FORMSTABLE COMPLEXES
STRINGENT HYBRIDIZATION REDUCED-STRINGENCY HYBRIDIZATION
A
Textbook: Figure 5.8
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Electrophoresis of DNA
Voltage
+
DNA fragments loaded into wells
Path of migration
DNA fragmentsseparate by size
and charge
_
Electrophoresis
Restriction enzymedigestion
Principle of a Southern blothybridize labeled probe to fragment of DNA
Add radio-labelednormal DNA
probes
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Polymerase Chain Reaction(PCR)
Isolate anddenature DNA
Anneal andextend primers
Repeat asnecessary
Amplifiedsegments
Sequence to beamplified
DNA Sequencing
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5'3'
T G T T
C T G A C T T C G A C A A
SINGLE-STRANDED DNAOF UNKNOWN SEQUENCE
RADIOACTIVELY LABELEDPRIMER
O CH O2
H H
H H
HH
DIDEOXYNUCLEOTIDE (ddNTP)
DNA POLYMERASE I
dATP
dGTP
dCTP
dTTP
ddATP ddCTP ddTTP ddGTP
C T G A C T T C G A C A A
ddG
REACTIONMIXTURES
dd
AT
P
READ SEQUENCE OF ORIGINALSINGLE-STRANDED DNA(COMPLEMENT OF PRIMER-GENERATED SEQUENCE LADDER)
GELELECTROPHORESIS
AUTORADIOGRAPHYTO DETECT
RADIOACTIVE BANDS
3'5'
BASE
dd
CT
P
dd
TT
P
dd
GT
PLARGER
FRAGMENTS
SMALLERFRAGMENTS
C
T
G
A
CT
T
C
G
ddG
ddG
PRODUCTS IN ddGTP REACTION
PP P
Textbook: Figure 5.17
DNA Sequencing
ATC TTA GAG TGT CCC ATC TTA GTG TCC C
Start
A T C G
Normal Mutant (185delAG)
AG
A T C G
delA
Start
delG
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Learning Objectives (3)
• Know the basics of gene structure, function and regulation.
• Be familiar with the basic methods of molecular genetics.– nucleic acid hybridization– Southern (DNA) and northern (RNA) blotting– PCR and gel electrophoresis– DNA sequencing– basic steps involved in constructing & screening a cDNA library
• Understand the meaning of DNA sequence and amino acidpolymorphisms.
• DNA sequence analysis
• Transgenic technologies
Polymorphisms and Mutations• Sequence variation-- differences among individuals
(DNA, amino acid)– > 0.01 = polymorphism– < 0.01 = rare variant
• Mutation-- any change in DNA sequence– Silent vs. amino acid substitution vs. other– neutral vs. disease-causing
• Common but incorrect usage:
“mutation vs. polymorphism”
• balanced polymorphism= disease + polymorphism
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Learning Objectives (3)(continued)
• Understand the meaning and significance of DNAsequence and amino acid polymorphisms.
• Understand the various types of DNA sequencepolymorphisms.– RFLPs (Restriction Fragment Length Polymorphism)
– VNTRs (Variable Number Tandem Repeat)
– SSRs (Simple Sequence Repeat; also STR [Short/SimpleTandem Repeat]))
– SNPs (Single Nucleotide Polymorphism)
Textbook: Figure 5.19
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Learning Objectives (3)(continued)
• Understand the meaning and significance of DNAsequence and amino acid polymorphisms.
• Understand the various types of DNA sequencepolymorphisms.– RFLPs (Restriction Fragment Length Polymorphism)
– VNTRs (Variable Number Tandem Repeat)
– SSRs (Simple Sequence Repeat; also STR [Short/SimpleTandem Repeat]))
– SNPs (Single Nucleotide Polymorphism)
Disease-Associated Mutations Alter Protein Function
Functional protein Nonfunctional ormissing protein
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P1 P2(TCTA)10
(TCTA)11
(TCTA)12
(TCTA)13
(TCTA)14
(TCTA)15
A
B
C
D
E
F
AB CD EF AF CE
15
14
13
1211
10
Textbook: Figure 5.22
SNP (coding sequence)
NormalmRNA
Protein
A U G
Met
A A G
Lys
U U U
Phe
G G C
Gly
G C A
Ala
U U G
Leu
A A
Gln
C
Silent DNA sequence polymorphism
Sequencevariant
mRNA
ProteinA U G
Met
A A G
Lys
U U U
Phe
G G U
Gly
G C A
Ala
U U G
Leu
A A
Gln
C
G
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Disease-Associated Mutations
A mutation is a change in the normal base pair sequence
Commonly used to define DNA sequence changesthat alter protein function
PolymorphismDNA sequence changes that do not alter
protein function (common definition, not technically correct)
Functional protein Functional protein
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Polymorphism• Variation in population
– phenotype– genotype (DNA sequence polymorphism)
• Variant allele > 1%
“Normal”
Disease
< 1% > 1%
Rare or “private”polymorphism
polymorphism
Common usage:
disease ??Factor V R506Q: thrombosis, 3% allele frequency
THE BIG RED DOG RAN OUT.
THE BIG RAD DOG RAN OUT.
THE BIG RED.
THE BRE DDO GRA.
THE BIG RED ZDO GRA.
Mutations
Normal
Missense
Nonsense
Frameshift (deletion)
Frameshift (insertion)
Point mutation: a change in a single base pair
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Silent Sequence Variants
NormalmRNA
Protein
A U G
Met
A A G
Lys
U U U
Phe
G G C
Gly
G C A
Ala
U U G
Leu
A A
Gln
C
Sequence variant: a base pair change that does not change theamino acid sequence (a type of polymorphism)
Sequencevariant
mRNA
Protein
Adapted from Campbell NA (ed). Biology, 2nd ed, 1990
A U G
Met
A A G
Lys
U U U
Phe
G G U
Gly
G C A
Ala
U U G
Leu
A A
Gln
C
G
Missense Mutations
Missense
Missense: changes to a codon for another amino acid(can be harmful mutation or neutral polymorphism)
mRNA
Protein
NormalmRNA
Protein
A U G
Met
A A G
Lys
U U U
Phe
G G C
Gly
G C A
Ala
U U G
Leu
A U G
Met
A A G
Lys
U U U
Phe
A G C
Ser
G C A
Ala
U U G
Leu
A A
Gln
C
A A
Gln
C
Adapted from Campbell NA (ed). Biology, 2nd ed, 1990
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Nonsense Mutations
Nonsense: change from an amino acid codon to a stopcodon, producing a shortened protein
Nonsense
mRNA
Protein
NormalmRNA
Protein
A U G
Met
A A G
Lys
U U U
Phe
G G C
Gly
G C A
Ala
U U G
Leu
A U G
Met
U A G U U U G G C G C A U U G
A A
Gln
C
A AC
Adapted from Campbell NA (ed). Biology, 2nd ed, 1990
Frameshift Mutations
Frameshift U G C A AA U G
Met
A A G
Lys
G C G
Ala
C A UU U
U
G
Leu
Frameshift: insertion or deletion of base pairs, producing a stopcodon downstream and (usually) shortened protein
mRNA
Protein
NormalmRNA
Protein
A U G
Met
A A G
Lys
U U U
Phe
G G C
Gly
G C A
Ala
U U G
Leu
A A
Gln
C
Adapted from Campbell NA (ed). Biology, 2nd ed, 1990
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Splice-Site Mutations
Exon 1 Intron Exon 2 Intron Exon 3
Exon 1 Exon 3Altered mRNA
Splice-site mutation: a change that results in altered RNA sequence
Exon 2
Other Types of Mutations
• Mutations in regulatory regions of the gene
• Large deletions or insertions
• Chromosomal translocations or inversions
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Types of Mutations
• Point Mutations– Silent– Missense– Nonsense– (frameshift)
• Deletion/Insertion– small– large
• Rearrangement
• Transcription
• RNA Processing– splicing– poly A– RNA stability
• Protein level– processing– stability– altered function
• gain• loss• new
Learning Objectives (4)
• Know the basics of gene structure, function and regulation.
• Be familiar with the basic methods of molecular genetics.
• Understand the meaning of DNA sequence and amino acidpolymorphisms.
• Know how DNA sequence analysis is performed and befamiliar with methods of screening for differences. – SSCP– DGGE– CSGE– ASO– Chip technology
• methods for gene transfer and the power of transgenics
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Tests to Detect Unknown Mutations
• Used when a specific mutation has not beenpreviously identified in a family
• DNA sequencing is most informative method
• Simpler scanning tests also may be used, usuallyfollowed by limited sequencing to characterizethe specific mutation
Single Strand ConformationalPolymorphism (SSCP)
DNA
Gel
Normal Mutated
mutation
• DNA is denatured intosingle strands
• Single strands fold; shapeis altered by mutations
• Mobility of mutant andnormal strands differ ingel
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Evaluating SSCP
Pros
• Rapid, simple, and widelyavailable for many genes
• Detects 60%−95% ofmutations in short DNAstrands
Cons
• Subsequent DNA sequencingneeded to characterize mutation
• Sensitivity drops with longerDNA sequences
Denaturing Gradient GelElectrophoresis (DGGE)
• DNA denatured into singlestrands
• Single strands reanneal intonormal and mutanthomoduplexes andheteroduplexes
• Hetero- and homoduplexesdenature at different points ingradient gel
DNA
Denaturing gradient gel
Normal Mutated
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Denaturing Gradient Gel
1 normal homoduplex band2 heteroduplex bands1 mutant homoduplex band
BRCA1 mutation carrier
Evaluating DGGE
Pros• Highly sensitive (>90%)
• Better resolution than SSCP
Cons• Not efficient for
analyzing large DNAfragments
• Subsequent DNAsequencing needed tocharacterize mutation
• Labor-intensive set-up
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Heteroduplex Analysis (CSGE)
Normal band
Mutated bands
Single-strand DNACold
Reannealed DNA
Amplify anddenature
DNA
Evaluating HeteroduplexAnalysis
Pros
• >90% sensitivity
• Rapid, simple assay
• Easily automated for highthroughput use
Cons
• Subsequent sequencingneeded to characterizemutation
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Tests to Search for KnownMutations
• Used when a specific mutation is known or suspected tooccur in a family
• Methods focus on detection of one or a few specificmutations (eg, “Ashkenazi Jewish panel”)
• Methods include ASO, CSGE, restriction site digestion,others
Add radio-labelednormal DNA
probes
Amplify DNA and hybridizeto membranes
Allele Specific Oligonucleotide(ASO) Hybridization
Add knownmutant DNA
probes
Patients
#1 #2 #3
#1 #2 #3
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Evaluating ASO Analysis
Pros
• Sensitive method to detectknown mutations
• Panels of ASO probes usefulto detect common mutations
Cons
• Each ASO probe detectsonly one specific sequence
• Most useful for smallsequence changes
Principle of Microarray (Chip)Assay
Synthetic DNA probes
Prehybridization Posthybridization
Probes withhybridized DNA
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Mutation vs. Silent Sequence Variation
• Obvious disruption of gene– large deletion or rearrangement– frameshift– nonsense mutation
• Functional analysis of gene product– expression of recombinant protein– transgenic mice
• New mutation by phenotype and genotype
X
Learning Objectives (5)
• Know the basics of gene structure, function and regulation.
• Be familiar with the basic methods of molecular genetics.
• Understand the meaning of DNA sequence and amino acidpolymorphisms.
• Know how DNA sequence analysis is performed and befamiliar with methods of screening for differences.
• Have a general understanding of methods for gene transferinto tissue culture cells and the power of transgenictechnologies.
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REMOVE FERTILIZED OOCYTES FROM OVULATING MOUSE IMMEDIATELY
AFTER FERTILIZATION
REMOVE BLASTOCYSTS FROM PREGNANT MOUSE FOUR DAYS AFTER OVULATION
FEMALE PRONUCLEUSHOLDING PIPETTE
INJECTION NEEDLE IMPALING MALE PRONUCLEUS OF OOCYTE AND INJECTING DNA
OOCYTE
REIMPLANT SEVERAL OOCYTES IN FOSTER MOTHER
REIMPLANT SEVERAL BLASTOCYSTS IN FOSTER MOTHER
BIRTH
BIRTH
BIRTH
A
C
B
D
SOUTHERN BLOT OF TAIL DNA NORTHERN BLOT
BREEDING
A B C D
C
A
C
B
D
A B C D
SOUTHERN BLOT OF TAIL DNAA B C D
CULTURED ES CELLS WITH TARGETED GENE
ALTERATION
INJECT ES CELLS INTO BLASTOCYST
+
NORMAL GENE
ALTERED GENE
Summary
• Gene structure helps us understand where to look for errors.
• PCR and gel electrophoresis essential for diagnostic tests.
• DNA polymorphisms are best defined by frequency.
• Screening for DNA sequence differences is performed bydirect sequencing or other techniques that are selected basedon whether the mutation is known or unknown.
• Introduction to gene transfer provides a framework forlearning about gene therapy and methods for recombinantdrug development.