Lesson 6.1.3a
6.1.3a DNA sequencing and DNA profiling Quiz: OCR Biology, Unit 7
20 questions
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Lesson 6.1.3a, DNA sequencing and DNA profiling: 20 multiple choice questions for the OCR Biology (H020), Unit 7: Genetics and evolution, written with Revision Ninja.
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The 20 questions
-
Which modified nucleotides terminate chain extension in Sanger (dideoxy) sequencing?
- Ribonucleotides
- Free deoxyribose sugars
- Dideoxynucleotides
- Amino acids
-
Which region of the genome is primarily analysed during DNA profiling?
- Ribosomal RNA genes
- Structural centromeres
- Protein-coding exons
- Short tandem repeats
-
What is the correct order of stages in a single PCR cycle?
- Denaturation, annealing, extension
- Denaturation, extension, annealing
- Extension, annealing, denaturation
- Annealing, denaturation, extension
-
By which physical property are DNA fragments separated during standard gel electrophoresis?
- Charge
- Base composition
- Size
- Shape
-
Where do restriction endonucleases cut double-stranded DNA molecules?
- Specific recognition sites
- Terminal telomeres
- Non-coding introns
- Random base pairs
-
Which heat-stable DNA polymerase is commonly used in the polymerase chain reaction?
- Taq polymerase
- RNA polymerase
- Reverse transcriptase
- DNA ligase
-
What is the main purpose of adding primers in PCR?
- Join DNA fragments
- Provide a 3' end
- Denature target DNA
- Hydrolyse nucleotides
-
A single DNA molecule is subjected to 5 cycles of PCR, with each cycle doubling the DNA. How many copies are produced?
- 32
- 25
- 10
- 5
-
In gel electrophoresis, which DNA fragments move furthest towards the positive electrode?
- Largest fragments
- Smallest fragments
- Single-stranded fragments
- Circular plasmids
-
If ten independent loci each have a 1 in 10 match probability, what is the combined match probability?
- 1 in 10 billion
- 1 in 100
- 1 in 100 thousand
- 1 in 1 million
-
A linear DNA molecule is cut by a restriction enzyme at 3 sites. How many fragments are produced?
- 3
- 2
- 4
- 6
-
A forensic sample contains only about 1 ng of DNA. Which technique is used to increase the amount of DNA for profiling?
- Western blotting
- Electrophoresis alone
- Ultracentrifugation
- PCR
-
What happens when a dideoxynucleotide is incorporated into a growing DNA strand during sequencing?
- Chain termination occurs
- Transcription begins
- Strand unwinding starts
- Mutation rate increases
-
In Sanger sequencing, why do synthesised DNA fragments terminate at different lengths?
- Primer degradation
- Random dideoxynucleotide incorporation
- Variable gel temperature
- Enzyme denaturation
-
Why can a matching DNA profile not guarantee absolute 100% certainty of identity?
- Relatives share alleles
- Enzymes lack specificity
- DNA degrades instantly
- STRs are non-variable
-
Why is interpreting a DNA profile difficult when a sample contains DNA from multiple individuals?
- Gel melts
- Primers fail
- DNA unwinds
- Peaks overlap
-
A PCR begins with 4 cycles producing 16 copies. A sample starts with 500 copies and undergoes 6 cycles. How many copies result?
- 32000
- 6400
- 16000
- 3000
-
Why are short tandem repeats (STRs) useful in human DNA profiling?
- Found only on ribosomes
- Variable repeat numbers
- Code for vital enzymes
- Identical in all humans
-
Why is contamination particularly problematic when preparing samples for PCR amplification?
- Taq polymerase inhibits
- Contaminating DNA amplifies
- Primers digest sample
- DNA fragments dissolve
-
Which region of human DNA is primarily analysed during standard DNA profiling?
- Exons coding proteins
- Mitochondrial coding genes
- Ribosomal RNA genes
- Non-coding repeat sequences
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