Genetics and Molecular Biology Quiz

A colorful illustration of DNA strands intertwining with molecular structures, depicting key concepts of genetics and molecular biology, with a knowledge theme.

Genetics and Molecular Biology Quiz

Test your knowledge on DNA, mutations, and gene structures with our engaging quiz! This quiz covers a variety of topics in genetics that are essential for both students and enthusiasts alike.

  • Learn about DNA isolation techniques
  • Understand the impact of different types of mutations
  • Discover RNA processing and its significance
25 Questions6 MinutesCreated by AnalyzingGene123
Which cells can be used for DNA isolation
White blood cells
Red blood cells
Epithelial cells of oral cavity
Hair roots
Which reagent should be used to precipitate DNA
Ice-cold ethanol
Ice-cold isopropanol
Ammonium acetate
Phenol-chloroform mixture
In the gene structure we can find
5´UTR and 3´UTR
Promoter
Exons – non-coding sequence
Exons – coding sequence
Mutations which are due to a single nucleotide change in the DNA and lead to the replacement of one amino acid in a protein by another are
Nonsense mutations
Silent mutation
Missense mutations
Single base pair substitutions
What kind of mutation is shown in the example: • Normal: CAG GTG ACC TCA GTG • Altered: CAG GTG AGG CCT CAG TG
Missense mutation, GG deletion
Frameshift mutation, changed sequence of the protein
GG insertion
Silent mutation, no change of the protein
Missense mutations
Are DNA alterations that usually cause a disease
Are changes in DNA sequence
Can be caused by deletion of 1 nucleotide
Can be caused by substitution of 3 nucleotides
Which of the following can lead to a loss of gene function
A missense mutation
A silent mutation
A deletion of the first exon of the gene
A sequence change in the intron
Processing of RNA includes
Addition to a 5´ end the Cap structure
Addition of a poly A tail at the 3´ end
Splicing is removal of exons and the joining together of the introns
Splicing is the removal of introns and the joining together of the exons
Takes place in cytoplasm
The single base deletion is
Missense mutation
Nonsense mutation
Frameshift mutation
Silent mutation
No mutation
Insertion or deletion can cause in protein
Frameshift if deleted are two nucleotides
In-frame mutation if deleted are two nucleotides
Frameshift if inserted are three nucleotides
In-frame mutation if inserted is three nucleotides
Mark the protein coding parts of the gene
Promotor
Exons
Introns
UTR
Adding NaCl during DNA isolation causes
Removing membrane lipids
Removing proteins
Removing RNA
DNA dissolving
Mutations are
DNA alterations which do not damage protein function and structure
DNA alterations leading to protein inactivation and thus to a disease
Initiates the process of transcription
Changes to the nucleotides sequence of the genetic material of an organism
Replication
Takes place in nucleus before the cell division
Is a process of copying RNA
DNA helicase unwinds the DNA double helix
Requires RNA polymerase involvement
Mark the correct sequences
DNA contains sugar deoxyribose and base: A, T, G, C
DNA contains sugar deoxyribose and base: A, T, G, U
RNA contains sugar deoxyribose and base: A, T, G, C
RNA contains sugar ribose and base: A, G, U, C
Is it true that
Deletion of 200 000 nucleotides can be DNA polymorphism
Intronic 2bp substitution can lead to missense mutation
Nonsense mutation leads usually to protein truncation
3´UTR is usually located at the beginning of the last exon
A premature mRNA includes
Promotor
Exons
Introns
UTRs
Blood sample
Red blood cells at the bottom
Thin layer of leukocytes mixed with platelets in the middle
Blood plasma clear solution at the top layer
Red blood cells at the top
Blood plasma clear solution at the bottom
Choose the correct answer of replication process
DNA helicase unwind the DNA forming a structure called the replication fork
Primase is an enzyme that synthesizes short RNA sequences called primers
Okazaki fragments are created on leading – strand template
Replication starts from promotor TATA box
Which sentence of translation process is correct
UAG is start codon
Translation takes place in cytoplasm
TRNA is links with amino acid and recognize the appropriate mRNA codon
MRNA transfers genetic information from DNA to ribosomes
RNA-Interference
Blocks the translation
Blocks the transcription
Takes place inside the nucleus
RISC and Dicer are involved
Blocks expression of all genes
TATA BOX
Is present in DNA
Is present in RNA
Is the DNA initiation place for RNA synthesis
Is the initiation place for protein synthesis
Is part of last exon
5'UTR
Present in DNA
Present in RNA
Initiates the RNA synthesis
Initiates the protein synthesis
Is part of exon 1
Insertion or deletion can cause in protein
Frameshift if 2 nucleotides is deleted
In-frame mutation if deleted are 2 nucleotides
Frame-shift if inserted are 3 nucleotides
In-frame mutation if inserted are 3 nucleotides
Is it true that
DNA can be found in prokaryotes and eukaryotes
Eukaryotes are usually larger in size than prokaryotes
Organelles can only be found in eukaryotes
Prokaryotes don't have translation because they don't have a RER
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