Molecular genetics
  • 1. Molecular genetics is a branch of genetics that deals with the molecular structure and function of genes. It involves the study of DNA, RNA, and proteins to understand how genetic information is stored, replicated, and expressed in living organisms. By examining the molecular mechanisms underlying genetic traits and diseases, molecular genetics has profound implications for fields such as medicine, agriculture, and biotechnology. Researchers in this field use techniques such as DNA sequencing, gene editing, and gene expression analysis to investigate the role of specific genes in various biological processes. Overall, molecular genetics plays a crucial role in unraveling the complexities of heredity and advancing our understanding of genetic disorders and evolutionary relationships among species.

    Which of the following is not a component of a nucleotide?
A) Phosphate group
B) Sugar
C) Nitrogenous base
D) Amino acid
  • 2. What is the function of helicase in DNA replication?
A) Adds nucleotides to the growing DNA strand
B) Proofreads the newly synthesized DNA
C) Seals nicks in the DNA strand
D) Unwinds the DNA double helix
  • 3. Which enzyme is responsible for RNA synthesis in transcription?
A) DNA ligase
B) RNA polymerase
C) Helicase
D) Primase
  • 4. How many nucleotide bases are in a codon?
A) Five
B) Three
C) Two
D) Four
  • 5. What process involves the decoding of the mRNA sequence to build a protein?
A) Mutation
B) Replication
C) Translation
D) Transcription
  • 6. Which type of mutation results in a premature stop codon?
A) Silent mutation
B) Nonsense mutation
C) Frameshift mutation
D) Missense mutation
  • 7. Where does translation occur in a eukaryotic cell?
A) Endoplasmic reticulum
B) Nucleus
C) Golgi apparatus
D) Ribosome
  • 8. Which type of RNA carries amino acids to the ribosome during translation?
A) Ribosomal RNA (rRNA)
B) Transfer RNA (tRNA)
C) Small nuclear RNA (snRNA)
D) Messenger RNA (mRNA)
  • 9. Which type of mutation alters a single nucleotide?
A) Deletion mutation
B) Insertion mutation
C) Duplication mutation
D) Point mutation
  • 10. What is the process by which segments of DNA are cut and spliced together?
A) Recombination
B) Replication
C) Transcription
D) Translation
  • 11. Which enzyme is responsible for sealing nicks in the DNA strand during replication?
A) Topoisomerase
B) Helicase
C) DNA ligase
D) Primase
  • 12. What is the term for a change in the DNA sequence that results in a change in the amino acid sequence of a protein?
A) Missense mutation
B) Silent mutation
C) Nonsense mutation
D) Frameshift mutation
  • 13. Which organelle is responsible for protein folding and processing in eukaryotic cells?
A) Endoplasmic reticulum
B) Lysosome
C) Peroxisome
D) Mitochondria
  • 14. In eukaryotic cells, where is DNA located?
A) Nucleus
B) Cytoplasm
C) Mitochondria
D) Chloroplast
  • 15. What is the term for the process of copying genetic information from DNA to RNA?
A) Replication
B) Translation
C) Transcription
D) Mutation
  • 16. Which enzyme is responsible for adding nucleotides to the growing DNA strand during replication?
A) DNA polymerase
B) RNA polymerase
C) Helicase
D) Primase
  • 17. Which molecule carries the genetic instructions for the development, functioning, growth, and reproduction of all living organisms?
A) RNA
B) Carbohydrate
C) Protein
D) DNA
  • 18. What is the region on a DNA molecule where RNA polymerase binds to initiate transcription?
A) Exon
B) Intron
C) Promoter
D) Terminator
  • 19. What is the role of RNA splicing in gene expression?
A) Removal of introns and joining of exons
B) Initiation of translation
C) Start of transcription
D) Proofreading DNA
  • 20. What is the primary function of DNA ligase in DNA replication?
A) Joins Okazaki fragments on the lagging strand
B) Adds RNA primers
C) Unwinds the DNA double helix
D) Proofreads the newly synthesized DNA
  • 21. Which type of RNA is a component of the ribosome and facilitates protein synthesis?
A) Ribosomal RNA (rRNA)
B) Transfer RNA (tRNA)
C) Small nuclear RNA (snRNA)
D) Messenger RNA (mRNA)
  • 22. What is the process that ensures the accurate replication of DNA sequences?
A) Transcription
B) Transversion
C) Translocation
D) Proofreading
  • 23. Which enzyme is responsible for unwinding the DNA double helix during DNA replication?
A) Primase
B) RNA polymerase
C) DNA ligase
D) Helicase
  • 24. What type of bond holds the two strands of DNA together?
A) Covalent bonds
B) Hydrogen bonds
C) Ionic bonds
D) Van der Waals forces
  • 25. What is the term for a region of DNA that determines a specific trait?
A) Allele
B) Gene
C) Genome
D) Chromosome
  • 26. Which of the following is a type of chromosomal mutation?
A) Point mutation
B) Deletion
C) Silent mutation
D) Missense mutation
  • 27. What is the name of the process that generates multiple RNA transcripts from a single gene?
A) Polyadenylation
B) Alternative splicing
C) Transcription
D) Translation
  • 28. What molecule carries the genetic information from the nucleus to the cytoplasm in eukaryotic cells?
A) mRNA
B) rRNA
C) snRNA
D) tRNA
  • 29. Which DNA repair mechanism fixes thymine dimers caused by UV radiation?
A) Base excision repair
B) Mismatch repair
C) Nucleotide excision repair
D) Homologous recombination
  • 30. Which process involves the movement of genes from one chromosome to another?
A) Replication
B) Translation
C) Translocation
D) Mutation
  • 31. Which of the following is true about the genetic code?
A) Linear
B) Degenerate
C) Non-overlapping
D) Unambiguous
  • 32. What is the term for the conformational change in a protein due to extreme conditions like heat or pH?
A) Degradation
B) Denaturation
C) Glycosylation
D) Phosphorylation
  • 33. What is the term for a section of DNA that can move to other locations in the genome?
A) Telomere
B) Transposable element
C) Operon
D) Intron
  • 34. Which type of chromosomal mutation results in a portion of a chromosome being duplicated?
A) Translocation
B) Deletion
C) Duplication
D) Inversion
  • 35. What are the building blocks of DNA and RNA?
A) Fatty acids
B) Nucleotides
C) Amino acids
D) Monosaccharides
  • 36. Which term describes the genetic makeup of an individual?
A) Genotype
B) Chromosome
C) Allele
D) Phenotype
  • 37. What is the name for the three-nucleotide sequence on mRNA that codes for a specific amino acid?
A) Exon
B) Intron
C) Anticodon
D) Codon
  • 38. What is the process by which genetic material is copied before cell division?
A) Mutation
B) Transcription
C) Translation
D) Replication
  • 39. What is the term for the specific location of a gene on a chromosome?
A) Locus
B) Phenotype
C) Allele
D) Genotype
  • 40. Which genetic disorder results from an extra copy of chromosome 21?
A) Turner syndrome
B) Down syndrome
C) Cystic fibrosis
D) Klinefelter syndrome
  • 41. What is the name for the physical expression of an individual's genetic makeup?
A) Genotype
B) Locus
C) Allele
D) Phenotype
  • 42. Which type of mutation results in the insertion or deletion of a nucleotide?
A) Silent
B) Frameshift
C) Missense
D) Nonsense
  • 43. Which genetic disorder is caused by the presence of an extra X chromosome in males?
A) Klinefelter syndrome
B) Turner syndrome
C) Cystic fibrosis
D) Down syndrome
  • 44. What term describes an individual possessing two different alleles for a particular trait?
A) Heterozygous
B) Homozygous
C) Phenotype
D) Genotype
  • 45. Which type of mutation does not result in a change to the amino acid sequence of a protein?
A) Missense
B) Silent
C) Nonsense
D) Frameshift
  • 46. What term describes alternate forms of a gene that can result in different traits?
A) Phenotype
B) Locus
C) Genotype
D) Allele
  • 47. Which genetic disorder results from the absence of an X chromosome in females?
A) Klinefelter syndrome
B) Turner syndrome
C) Cystic fibrosis
D) Down syndrome
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