Unit 4: Advances in Molecular Biology & Genetics - Practice Quiz

BTY422 — Dissertation-I 60 Questions
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1 What is the primary molecule that stores genetic information in most living organisms?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. DNA
B. Glucose
C. Cellulose
D. Lipid

2 The process of copying DNA into a complementary RNA molecule is called:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Digestion
B. Translation
C. Transcription
D. Replication

3 Which technique is widely used to amplify specific DNA sequences in the laboratory?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. PCR
B. Gram staining
C. ELISA
D. Chromatography

4 In the DNA double helix, adenine (A) pairs with which base?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Uracil
B. Guanine
C. Thymine
D. Cytosine

5 The CRISPR-Cas9 system is primarily used for:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Cell counting
B. Protein staining
C. Genome editing
D. pH measurement

6 Which sugar is found in RNA but not in DNA?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Deoxyribose
B. Glucose
C. Fructose
D. Ribose

7 The complete set of genes in an organism is known as its:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Genome
B. Proteome
C. Ribosome
D. Cytoplasm

8 Translation is the process by which:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. DNA is copied into DNA
B. Proteins are broken down
C. mRNA is decoded to build a protein
D. RNA is copied into DNA

9 Which enzyme is responsible for synthesizing new DNA strands during replication?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. DNA polymerase
B. RNA polymerase
C. Ligase only
D. Amylase

10 Gel electrophoresis separates DNA fragments primarily based on their:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Size
B. Temperature
C. Taste
D. Color

11 A change in the DNA sequence of a gene is called a:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Mutation
B. Digestion
C. Transcription
D. Translation

12 Which base found in RNA replaces thymine of DNA?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Cytosine
B. Uracil
C. Adenine
D. Guanine

13 The 'central dogma' of molecular biology describes the flow of information from:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. DNA to RNA to Protein
B. Protein to RNA to DNA
C. Protein to DNA to RNA
D. RNA to DNA to Protein

14 Restriction enzymes are used in molecular biology to:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Stain cells
B. Measure pH
C. Join amino acids
D. Cut DNA at specific sequences

15 A gene is best defined as a:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Segment of DNA that codes for a product
B. Kind of sugar
C. Cell organelle
D. Type of protein

16 Which technology allows scientists to insert a gene from one organism into another?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Distillation
B. Centrifugation
C. Filtration
D. Recombinant DNA technology

17 The set of three nucleotides that codes for a specific amino acid is called a:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Codon
B. Ribosome
C. Chromosome
D. Gene

18 Sequencing of the entire human genome was completed under which major project?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Apollo Project
B. Genome Recycling Project
C. Manhattan Project
D. Human Genome Project

19 Which structure carries genes and is composed of DNA and protein?

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Lysosome
B. Vacuole
C. Chromosome
D. Ribosome

20 The study of how gene expression changes without altering the DNA sequence is called:

Discussion on thrust research area- Molecular Biology and Genetics Easy
A. Epigenetics
B. Anatomy
C. Taxonomy
D. Ecology

21 A researcher wants to selectively amplify a specific 500 bp region from genomic DNA before sequencing. Which technique is most appropriate as the first step?

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Polymerase Chain Reaction (PCR)
B. Southern blotting
C. Isoelectric focusing
D. Gel filtration chromatography

22 In CRISPR-Cas9 genome editing, the guide RNA primarily functions to:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Synthesize the new complementary strand
B. Ligate the cleaved DNA ends together
C. Add methyl groups to cytosine bases
D. Direct Cas9 to the complementary target DNA sequence

23 A gene of interest shows high mRNA levels but very low protein output in a cell. Which mechanism most likely explains this observation?

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Enhanced DNA replication
B. Translational repression by microRNAs
C. Loss of the promoter region
D. Increased transcription initiation

24 During a study, a scientist observes that a restriction enzyme cuts a plasmid at a single site, linearizing it. What can be inferred about the recognition sequence?

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. It occurs at every base pair
B. It is absent from the plasmid
C. It is methylated at all sites
D. It occurs only once in the plasmid

25 In quantitative real-time PCR (qPCR), a lower cycle threshold () value indicates:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. A higher initial amount of target template
B. Presence of primer dimers only
C. Failure of the amplification reaction
D. A lower initial amount of target template

26 A transgenic plant is engineered to express a bacterial gene. For the gene to be expressed correctly, the construct must include a:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Restriction site at every codon
B. Prokaryotic origin of replication only
C. Bacterial ribosome binding site only
D. Eukaryotic promoter recognized by the host

27 RNA interference (RNAi) is being used to knock down a target gene. The functional molecule that guides degradation of the target mRNA is:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. A histone protein complex
B. A double-stranded DNA probe
C. A ribosomal subunit
D. A small interfering RNA (siRNA) loaded into RISC

28 A DNA sample analyzed by gel electrophoresis migrates faster than a known 1 kb marker. This suggests the sample fragment is:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Smaller than 1 kb
B. Larger than 1 kb
C. Circular and supercoiled only
D. Exactly 1 kb

29 A point mutation changes a codon from UAC to UAA. What is the most likely consequence for the protein?

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Frameshift of the reading frame
B. A silent change with no effect
C. Premature termination of translation
D. Addition of an extra amino acid

30 In a Western blot experiment, the antibodies are used to detect:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Specific proteins
B. Specific DNA sequences
C. Specific RNA transcripts
D. Whole intact cells

31 A researcher observes that a gene is silenced without any change in its DNA sequence, and silencing is heritable across cell divisions. This is best explained by:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. A nonsense mutation in the promoter
B. A frameshift deletion in the coding region
C. Epigenetic modification such as DNA methylation
D. Loss of the entire chromosome

32 Next-generation sequencing (NGS) offers a major advantage over Sanger sequencing primarily because it enables:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Reading only one fragment at a time
B. Massively parallel sequencing of many fragments
C. Detection of proteins directly
D. Amplification without primers

33 A cloning vector must contain a selectable marker so that researchers can:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Increase the vector's copy number
B. Cut the insert DNA precisely
C. Translate the insert into protein
D. Identify cells that took up the vector

34 In a diploid organism, an autosomal recessive disease allele has frequency . Under Hardy-Weinberg equilibrium, the expected frequency of affected individuals is:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A.
B.
C.
D.

35 A reverse transcriptase enzyme is essential in cDNA synthesis because it:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Synthesizes DNA from an RNA template
B. Degrades single-stranded DNA
C. Synthesizes RNA from a DNA template
D. Adds a poly-A tail to mRNA

36 A microarray experiment shows a set of genes strongly upregulated after drug treatment. The most direct interpretation is that the drug increased:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. mRNA levels of those genes
B. The cell membrane permeability only
C. The DNA copy number of the genome
D. Protein degradation of those genes

37 Two genes located close together on the same chromosome tend to be inherited together. This phenomenon is called:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Random mutation
B. Genetic linkage
C. Independent assortment
D. Genetic drift

38 A researcher uses a GFP reporter fused to a promoter to study gene expression. Fluorescence intensity in the cells serves as a measure of:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Cell membrane integrity
B. Ribosome number
C. DNA replication rate
D. Promoter activity

39 During DNA replication, the leading and lagging strands differ because DNA polymerase can only synthesize DNA in the:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. direction
B. Both directions equally
C. Direction set by RNA polymerase
D. direction

40 A knockout mouse is generated to study a gene's function. The expected outcome of a successful knockout is:

Discussion on thrust research area- Molecular Biology and Genetics Medium
A. Random silencing of all genes
B. Duplication of the targeted gene
C. Loss of function of the targeted gene
D. Overexpression of the targeted gene

41 In a CRISPR-Cas9 experiment, a researcher observes high off-target cleavage. Switching to a high-fidelity Cas9 variant (e.g., HiFi-Cas9) reduces off-targets but also lowers on-target efficiency. Which mechanistic explanation best accounts for this trade-off?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. High-fidelity variants block PAM recognition entirely, preventing target engagement
B. High-fidelity variants convert Cas9 into a nickase, halving cleavage everywhere
C. High-fidelity variants increase gRNA degradation, reducing all cleavage uniformly
D. High-fidelity variants weaken non-specific DNA contacts, raising the energetic threshold for stable R-loop formation at both mismatched and perfectly matched sites

42 A gene with two alleles shows allele frequencies and . Under Hardy–Weinberg equilibrium, a researcher finds the observed heterozygote frequency is instead of the expected value. What is the fixation index ?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A.
B.
C.
D.

43 During RNA-seq analysis, a lncRNA shows strong nuclear enrichment and physically associates with chromatin-modifying complexes. Which functional hypothesis is most strongly supported by these data alone?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. It acts as a scaffold guiding epigenetic modifiers to specific genomic loci
B. It functions primarily as a miRNA sponge in the cytoplasm
C. It is translated into a small regulatory peptide
D. It serves mainly as a template for reverse transcription

44 A qPCR experiment yields a standard curve with slope . What is the approximate amplification efficiency, and what does it indicate?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. ; ideal doubling each cycle
B. ; failed reaction requiring redesign
C. ; sub-optimal efficiency, possibly due to inhibitors or primer issues
D. ; over-amplification artifact

45 A two-point cross gives a recombination frequency of 12% between loci A and B, and 8% between B and C. A three-point cross between A and C gives 18%. What does this discrepancy most likely indicate?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Double crossovers between A and C are undetected in the direct A–C measurement
B. Gene C is a transposable element
C. The loci are on different chromosomes
D. Recombination frequency exceeds 50% between A and C

46 In next-generation sequencing, a variant appears at 3% allele frequency in a tumor sample with 500x coverage. Why might this be a challenging call even at high depth?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Sequencing error rates can approach the variant frequency, requiring error models to distinguish true low-frequency somatic variants
B. The variant must be a germline polymorphism
C. High coverage always guarantees accurate low-frequency calls
D. Allele frequencies below 5% cannot exist biologically

47 A protein-coding gene undergoes alternative splicing producing an isoform lacking exon 5, which contains a stop codon in the retained transcript. The full-length mRNA is degraded, while the skipped isoform is stable. This regulation is best described as:

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Alternative splicing coupled to nonsense-mediated decay (AS-NMD) controlling protein output
B. Simple transcriptional repression of the gene
C. RNA editing introducing a premature stop codon
D. Post-translational proteasomal degradation of the isoform

48 A researcher performs ChIP-seq for a transcription factor and finds strong binding peaks in regions lacking the canonical motif. Which explanation is most plausible?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. The antibody has zero cross-reactivity, so peaks are false
B. The peaks represent sequencing adapter contamination only
C. Indirect recruitment via protein–protein interactions tethering the factor to DNA
D. Transcription factors never bind without motifs

49 In a bisulfite sequencing experiment, a CpG island shows near-complete conversion of cytosines to uracil except at specific sites. What do the unconverted cytosines indicate?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Those cytosines are unmethylated and freely converted
B. Those positions contain thymine, not cytosine
C. Those cytosines are 5-methylated, protecting them from bisulfite conversion
D. The bisulfite reaction failed entirely

50 A quantitative trait shows broad-sense heritability but narrow-sense heritability . What does this gap most directly imply for a selective breeding program?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Selection will produce rapid, predictable gains
B. Much of the genetic variance is non-additive (dominance/epistasis), limiting response to selection
C. The trait is entirely environmentally determined
D. The trait has no genetic basis

51 A GWAS identifies a significant SNP in an intergenic region far from any gene. Which follow-up interpretation is most scientifically sound?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Intergenic SNPs cannot influence phenotype
B. The SNP may tag a regulatory element or be in linkage disequilibrium with the causal variant
C. The association must be a statistical artifact since it is intergenic
D. The SNP is definitely the causal mutation altering protein sequence

52 During cloning, a researcher fails to obtain recombinant colonies despite successful ligation. The vector self-ligates efficiently. Which strategy most directly reduces vector self-ligation?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Increasing the ligase concentration tenfold
B. Extending the ligation incubation time
C. Using a lower insert-to-vector ratio
D. Dephosphorylation of the linearized vector 5' ends with alkaline phosphatase

53 A single-cell RNA-seq dataset shows a cluster of cells with high mitochondrial gene content and low total counts. What is the most appropriate interpretation before downstream analysis?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. These likely represent stressed or dying cells and should be filtered as quality-control artifacts
B. These cells have the highest data quality
C. Mitochondrial content is irrelevant to scRNA-seq QC
D. These are a novel high-metabolism cell type to prioritize

54 A knockout mouse for a gene shows no phenotype, yet the gene is highly conserved across vertebrates. Which explanation best reconciles conservation with the absence of a phenotype?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Conservation is meaningless for function
B. The knockout was incomplete in all tissues by definition
C. Functional redundancy from paralogs may compensate under standard laboratory conditions
D. Conserved genes never produce visible phenotypes

55 In a codon optimization strategy for heterologous protein expression, replacing rare codons with frequent ones sometimes reduces protein solubility. What is the most likely mechanistic cause?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Faster translation can disrupt co-translational folding rhythms encoded by rare-codon-induced pausing
B. Rare codons increase mRNA stability tenfold
C. Frequent codons introduce premature stop codons
D. Codon changes always alter the amino acid sequence

56 A researcher uses RNAi and observes off-target phenotypes. Which property of the siRNA most commonly drives these off-target effects?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. The length of the siRNA being exactly 21 nt
B. Seed-region (positions 2–8) complementarity to unintended mRNA 3' UTRs, acting miRNA-like
C. Perfect full-length complementarity to the intended target only
D. The siRNA being double-stranded

57 A mutation in a splice donor site (GT) at an intron boundary is identified. Which outcome is LEAST likely to result from this mutation?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Activation of a cryptic splice site nearby
B. Introduction of a synonymous change with no effect on the mRNA
C. Intron retention in the mature transcript
D. Exon skipping of the adjacent exon

58 In differential expression analysis with limited replicates, why do methods like DESeq2 model counts with a negative binomial rather than a Poisson distribution?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. The Poisson distribution cannot handle integer counts
B. The negative binomial requires no dispersion estimation
C. RNA-seq counts always have variance equal to the mean
D. The negative binomial accommodates overdispersion where variance exceeds the mean in RNA-seq counts

59 A base editor (cytosine base editor) is used to install a C→T edit but produces unexpected edits at nearby cytosines within the target window. What is the primary cause?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. The deaminase acts on all accessible cytosines within the single-stranded R-loop editing window (bystander editing)
B. The gRNA anneals to multiple genomic sites simultaneously
C. The base editor reverts edits during replication
D. The Cas9 nuclease cuts both strands randomly

60 A pedigree shows a trait transmitted only through mothers to all offspring, with variable severity among siblings. Which inheritance pattern and phenomenon best explain this?

Discussion on thrust research area- Molecular Biology and Genetics Hard
A. Genomic imprinting of a paternal allele
B. Mitochondrial inheritance with heteroplasmy causing variable expressivity
C. Autosomal dominant with complete penetrance
D. X-linked recessive inheritance