ABB HCLD Molecular Diagnostics COPY Flashcards
(134 cards)
1
Q
Molecular Diagnostics is a universal Technology affecting what areas?
A
Genetics, Infectious Disease, Heme Oncology, Identity Testing
2
Q
What is an infectious disease impacted by molecular diagnostics?
A
TB and other hard to culture organisms. These could take weeks to culture.
3
Q
What is a diploid genome?
A
Two sets of chromosomes
4
Q
How many pairs of chromosomes?
A
23 pairs, 22 pairs autosomes, 2 sex chromosomes
5
Q
How many bases make up the human Genome?
A
3 billion
6
Q
How many genes in the human genome?
A
22,000
7
Q
How much of the human genome codes for proteins?
A
10%
8
Q
Heterochromain
A
Densely packed region of chromosomes, like centromeres, not transcribed
9
Q
Euchromain
A
Less densely packed region of chromosomes, transcribed
10
Q
Antiparallel structure
A
5’ - 3’ and 3’ - 5’
11
Q
A NUCEOTIDE is made up of :
A
A 5-carbon sugar, a phosphate and a nitrogenous base
12
Q
Pyrimidine
A
A 6-member ring, Cytosine, Thymine, Uracil
13
Q
Purine
A
Fused 5 and 6-member rings, Adenine, and Guanine
14
Q
Difference between deoxyribose and ribose
A
Deoxyribose is missing an hydroxyl group in lower right corner
15
Q
Mitochondrial DNA, how many bases and how many genes?
A
16.5K bases, 37 genes
16
Q
What are some mitochondrial genes?
A
rRNA, tRNA, cytochrome C and ATP synthase
17
Q
What is a locus?
A
The location of the gene on the chromosome
18
Q
What is an allele?
A
Version of the gene present at any locus
19
Q
Polymorphism
A
Benign change in the genome, almost everyone has them
20
Q
Mutation
A
Present in a low percentage of people, role in disease
21
Q
How often do SNP’s occur in the genome?
A
Every 300bp or 10 million per genome
22
Q
What is a synonymous polymorphism?
A
A silent variant, the substitution does not change the amino acid.
23
Q
What is a non-synonymous polymorphism?
A
The substitution does change the amino acid.
24
Q
What is a somatic mutation?
A
Mutation that is acquired in non-germline cells, not inheritable,
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What is a germline mutation?
Mutations occur in germline cells, they are inheritable,
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What are structural mutations?
Translocations, Rearrangements, gene amplifications
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What are molecular mutations?
Insertions, deletions, point mutations, nucleotide repeats
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What is aneuploidy?
Whole chromosome loss or gain
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What is a duplication?
An area of gene sequence is repeated, can visualize with FISH
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What does a chromosome microarray show you?
Virtual or digital karyotype, millions of probes on a chip highlight areas of the chromosome where there could be abnormalities. Allows you to look for gains or losses in the genome.
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What is a Duplication?
An area of gene sequence is repeated, visualize with FISH.
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What is a Translocation?
An area of one chromosome is transferred to another chromosome, like BCR-ABL. Visualize with FISH or real-time PCR or NGS.
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What is a point mutation?
A single nucleotide substitution, insertion or deletion.
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What is a transition mutation?
A purine is substituted for a purine. A pyrimidine is substituted for a pyrimidine.
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What is a transversion mutation?
A purine is substituted for a pyrimidine. A pyrimidine is substituted for a purine.
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What is a missense mutation?
A base substitution that alters the codon resulting in a different amino acid.
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What is a nonsense mutation?
A base substitution that alters the codon resulting in a stop codon.
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What is a silent mutation?
Alters the codon, but not the amino acid
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What is a neutral mutation?
Alters the amino acid to a similar amino acid which does not disrupt the protein.
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What is a frameshift mutation?
Insertion or deletion of one or more bases which alters the codon reading frame changes protein structure
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Sickle cell anemia is caused by:
A single point mutation in the hemoglobin gene
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What is a splice site mutation:
Mutation alters the exon intron splice site, leads to exon skipping or intron inclusion
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What is the universal genetic code?
The different codons that form the amino acids.
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What a loss of function mutation?
Leads to complete or partial loss of protein function. Frequently recessive.
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What a gain of function mutation?
Causes an entirely new trait which can appear in inappropriate tissue or at inappropriate time in development. Frequently dominant.
46
Quantity of DNA from UV Spectrophotometry?
(A260-A320) * dilution factor * 50 ug/mL
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Quantity of RNA from UV Spectrophotometry?
(A260-A320) * dilution factor * 40 ug/mL
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Quality of DNA by UV Spectrophotometry?
(A260/A280) = purity
(A260-A320) / (A280-A320)
1.7-2.0 = good quality
<1.7 = too much protein
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How to look at quality with respect to size?
Gel electrophoresis
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Maxam - Gilbert sequencing
Used a toxic chemical and never really caught on
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Sanger sequencing technique
Chain termination sequencing using dideoxy method
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Difference between deoxy and dideoxy
Dideoxyribonucleic acid is missing a hydroxl group and more dNTP's cant add on so chain terminates
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Capillary Sequencing Technique
Separate bands in the gel capillary, excite fluorescent tag with Argon laser, Fluorescent light is shown through a prism to separated the colors.
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How does Ion Torrent Sequencing work?
Tagged DNA fragments are mixed with oil droplets, inside each oil droplet there is a sphere with DNA sequences that match the adaptors. Fragments bind to sphere and are PCR amplified inside the oil droplet. Each sphere is spun down into the chip. Sequencer floods the chip with a certain dNTP and measures the pH.
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How does Illumina work?
Seguencing by synthesis. Adapters cause DNA fragments to bind to the surface of the flow cell. Adapter at other end of the fragment bends over and binds forming a bridge. Synthesis occurs and amplifies the fragments, makes many copies and you visualize fluorescence.
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What is the clinical exome?
About 4000 genes associated with human disease
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What is the whole exome?
Where you sequence all 20,000 genes
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Whole genomes
All introns and exons and everything
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What are the steps in a Southern Blot?
1. Extract DNA
2. Restriction Enzyme digest
3. Gel electrophoresis
4. Denature DNA and transfer the gel to a membrane
5. Denature and hybridize a tagged probe to the membrane
6. Detect tagged probe
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Limitations of Southern Blot?
1. Need high molecular weight DNA
2. Takes a long time
3. Labor intensive
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How do you label your Southern probe
Nick translation (radioactive nucleotides) (Chemiluminescent), random primers
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What types of genetic abnormalities will a Southern detect?
Large insertions and deletions.
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What is probe Stringency?
Conditions of hybridization that control the specificity of binding between the probe and the target. Increase temperature or ionic strength to increase stringency.
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What is LCR?
Ligase chain reaction
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What is NASBA?
Nucleic Acid Sequence based amplification
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What is TMA?
Transcription mediate amplification
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What is SDA?
Strand displacement Amplification
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What is bDNA?
Branched DNA, signal amplification
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What is HCA?
Hybrid capture, signal amplification
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What does Magnesium do in a PRC reactions?
Stabilizes primer template interactions.
Stabilizes replication complex polymerase with the primer template.
Can increase non-specific annealing.
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Does Taq polymerase have proofreading?
No proofreading 3'-5' exonuclease activity
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What do you have to consider when selecting primers?
Keep them around 50% GC, Avoid G and C at 3' end (decreases primer dimers and non-specific annealing), Check primer end for complementarity.
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Does Taq polymerase have proofreading?
No proofreading 3'-5' exonuclease activity
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What is the formula for calculating how many copies you make by PCR?
Amplicons = Starting copy number * 2^(# cycles-2)
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Advantages of real-time PCR over PCR and gel electrophoresis.
1. Rapid target ID
2. Eliminates post-PCR processing
3. Highly specific with probes
4. Allows for multiplexing
5. Allows for quantification, amount of signal is proportional to the amount of DNA
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Delta Ct formula for fold differences
Delta Ct = (Ct of A) - (Ct of B)
Fold difference = 2^ delta Ct
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Digital Droplet PCR
Single molecule amplification in droplets of oil, count positive droplets to get absolute quantification of target sequence
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MPN stands for
Myeloproliferative Neoplasm
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BCR-ABL positive indicates
CML
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BCR-ABL negative indicates
PV, ET, MF
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Gleevec
Small molecule drug that binds to the BCR-ABL fusion gene and shuts off the overactive kinase activity.
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Why is BCR-ABL RT-PCR better at monitoring these patients than FISH or Karyotype
Its more sensitive and quantitative.
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Polycythemia Vera (PV) is
A myeloproliferative disease, MPD characterized by overproduction of RBC's
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Essential Thrombocythemia (ET) and Chronic Idiopathic Myelofibrosis (CIMF)
Are related MPD's
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The JAK2 mutation is present in:
The majority of PV and about half of ET and CIMF.
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The role of JAK2 is
a tyrosine kinase involved in signal transduction for multiple hematopoietic growth factors
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Myeloid Diseases
Are clonal diseases of hematopoietic stem cells or progenitor cells, derived from a single progenitor cell with a genetic abnormality
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Myeloid diseases are caused by:
Genetic or epigenetic alterations that perturb key processes such as self-renewal, proliferation, and differentiation
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What genes are associated with AML?
FLT3, NPM1, CEBPA
Prognostic: IDH1, IDH2, TET2, RUNX1
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What genes are associated with MDS?
KRAS, NRAS, IDH's, TET2, RUNX1
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PGXm, pharmacokinetic
M = metabolism
What the body does to the drug. Absorption, distribution, excretion.
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Mutations affecting PGXm
Polymorphisms, not typically disease causing mutations
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PGXt, targeted therapeutic
T = whether you have the target
Presence or absence of the target, resistance, lack of response
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Mutations affecting PGXt
Mutations in disease causing genes, driver and passenger genes. Germline or somatic
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Using polymorphisms affecting drug metabolism:
You can predict the spectrum of drug metabolism.
1. Ultra rapid metabolizers will have to take 100x more to get any affect.
2. Poor metabolizers will probably overdose
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Irinotecan for colon cancer (PGXm)
Toxicity to UGT1A1 deficiency. Normally the drug is inactivated by UGT1A1.
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Promoter of UGT1A1
Has TA repeats in the promoter in varying numbers TA7 causes reduced activity of UGT1A1. Detect by capillary electrophoresis.
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Tamoxifen for breast cancer (PGXm)
Toxicity to CYP2D6 deficiency
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Examples of PGXt drugs:
Gleevec for BCR-ABL
Herceptin for HER2 receptor in amplified breast cancer
Cetuximab for KRAS mutations
Tarceva for EGFR mutations
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Mutations can be detected in any sample type
Germline mutations
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Autosomal dominant inheritance
1. Affected individuals have at least one affected parent.
2. Each child of an affected parent has a 50% chance of inheriting the mutation
3. Unaffected people have unaffected children
4. males and females are affected equally
5. Inheritance pattern is vertical
102
Autosomal recessive inheritance
1. Affected members of the family are usually siblings of the proband.
2. Carrier parents have a 25% chance of having an affected child
3. Affected people may have unaffected parents (skips generations)
4. Inheritance pattern is horizontal
103
X-Linked Dominant
1. Female offspring of affected males will be affected
2. No male offspring of affected males will be affected
3. An affected female has a 50% chance of having an affected child.
4. All affected individuals have an affected parent
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X-Linked Recessive
1. Affected individuals are primarily males
2. All female offspring of affected males will be carriers
3. Male offspring of affected males will be unaffected
4. Inheritance pattern is not vertical of horizontal
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Heterogeneity
When a disease is caused by multiple mutations in the same gene or different genes
106
Anticipation
A progressive increase in severity in future generations
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Imprinting
Different expression of a mutant gene depending on if it was inherited by the mother or the father
108
Alpha-1-trypsin deficiency (ATT)
Causes genetic COPD and early onset emphysema
One of the most common genetic disorders affecting Caucasians and associated with childhood liver disorder. Only 6% of severe ATT is diagnosed
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Normal A1AT
Keeps neutrophil elastase in check
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A1AT Deficiency
Neutrophil elastase becomes a burden and attacks lung tissue
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Detect A1AT mutations by
allelic Discrimination
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Fragile X Syndrome
Most common form of inherited mental retardation and autism.
First example of trinucleotide repeat (CGG) expansion mutation
Maternally inherited with incomplete penetrance
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Symptoms of Fragile X Syndrome
Mental retardation, delayed speech, hyperactivity, anxiety, attention deficit, long narrow face, big ears, large testes
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Incidence of Fragile X
1:4000 males, 1:6000 Females
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FMR-1 gene encodes for
Fragile X mental retardation protein (FXMRP), role in protein synthesis in neurons, and dendritic development
116
CGG repeat involved in upstream methylation
Normal people have 5-45 copies
Fragile X individuals have >200 copies
Premutation or carrier state have 55-200
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How to detect?
Capillary electrophoresis, and PCR
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Another Trinucleotide repeat disorder
Huntington Disease
119
Affymetrix chromosomal microarray
2.6 million probes, 750,000 SNPs
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Digitized karyotype
The software looks at probe binding and flags areas of the chromosome where there might be issues.
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LCSH
Long Continuous Stretches of Homozygosity
Indicates parents were related.
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WES
Whole Exome Sequencing
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What is Parvovirus B19?
1. Small single stranded DNA virus.
2. Non-enveloped icosahedral particles
3. Replicates in actively dividing committed erythroid precursor cells in bone marrow
4. Destroys RBC's
5. Transmitted via respiratory route
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Parvovirus B19 symptoms
1. Fever chills headache myalgia, muscle soreness (First 7 days)
2. Rash, arthralgia, joint stiffness (day 21-28)
3. Anemia
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Utility of PCR testing for parvovirus?
1. Diagnose parvovirus infection as the causative agent in fetal hydrops (fluid retention)
2. Diagnose parvo in immunosuppressed patients
3. Diagnose parvo prior to seroconversion
4. Determine ideology of acute and chronic anemias
126
q PCR
Quantitative Real-Time PCR
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Fold difference in amount of target
Delta Ct method, 2^ delta Ct - fold difference
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Delta delta Ct
delta Ct = Ct(target A-treated) - Ct(Ref B-treated)
delta Ct = Ct(target A-control - Ct(Ref B-control)
delta delta Ct= delta Ct (treated) - delta Ct (control)
= Normalized target gene expression =
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Absolute Quantification
Using a standard curve to calculate how much of a target is present
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Characteristics of HIV
Icosahedral (20 sided), enveloped virus in the retrovirus family (RNA transcribed to DNA).
Two viral strands of RNA in core surrounded by outer protein coat.
Outer envelope has a lipid matrix embedded with glycoproteins which bind to target cell.
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Three main structural genes in HIV
1. Gag gene - Group Specific Antigen
2. Env - Envelope
3. Pol - Polymerase
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HIV life cycle
Virus enters host cell, RNA is reverse transcribed into DNA which incorporates into host DNA. As host cell replicates, it starts churning out viral particles.
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HIV drugs that target life cycle steps
Nucleoside Analogues and Non-nucleosides target the reverse transcriptase.
Protease Inhibitors stop virus particle building.
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Units of HIV Viral Load
log (copies/mL)
