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Question 1
Incorrect
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Which of the following is not true regarding mitochondrial chromosome disorders?
Your Answer: Mitochondrial chromosome defects are inherited from one’s mother
Correct Answer: Because mitochondrial chromosomes have no introns in their genes, any point mutation has a low likelihood of having an effect.
Explanation:Any point mutation in any part of the mitochondrial DNA will lead to a mutated mitochondria and will likewise have its ill effect on the body.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 2
Incorrect
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Which statement is incorrect?
Your Answer: AAUAAA acts as a cleavage signal for endonucleases.
Correct Answer: Translation begins when the triplet (UGA) encoding for methionine is encountered.
Explanation:Translation being when the codon for methionine is encountered which is AUG not UGA. This process is known as initiation. All the other options are correct.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 3
Incorrect
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What is the role of cyclin and cyklin-dependent kinases in mitosis:
Your Answer: Activation of growth factors
Correct Answer: Phosphorylation of proteins that make up pre-replication complexes
Explanation:There are certain regulators of the cell cycles that mediate progression through the cell cycle. These are cyclins and cyklin-dependent kinases (CDKs). They form a complex that phosphorylates protein involved in the cell cycle.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 4
Incorrect
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Regarding Polymerase Chain Reaction, all are true except:
Your Answer: DNA is initially denatured by heat into single stranded DNA prior to cooling
Correct Answer: There is a linear rise of DNA copies during amplification.
Explanation:All are true except there is a linear rise of DNA copies during amplification. There is an exponential rise in amplification of DNA.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 5
Incorrect
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When 2 nucleotide chains of DNA bind together, thymine is bound to:
Your Answer: Hydrogen
Correct Answer: Adenine
Explanation:As a general rule in the structure of DNA, thymine always binds to adenine with two hydrogen bonds, cytosine always binds to guanine with three hydrogen bonds and vice versa. However In the structure of RNA the only difference is that adenine binds to uracil instead of thymine. But thymine will always bind to adenine.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 6
Incorrect
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“Ploidy” is a term used to refer to the number of chromosomes in cells. Cancer cells are commonly:
Your Answer: Diploidy
Correct Answer: Aneuploidy
Explanation:Cancer cells most commonly undergo disordered cell growth and cell division. This results in an additional number of chromosomes called aneuploidy. This is a characteristic of cancer cells along with variation in differentiation of the cells.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 7
Correct
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Male to male transmission is a key factor of which type of inheritance?
Your Answer: Autosomal dominant
Explanation:Autosomal dominant type of inheritance can include both sexes in the same ratio. There is no skipping a generation and father to son transmission is common. The passing of the trait is sex independent.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 8
Incorrect
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In DNA cloning and sequencing, the bases in nucleotides chains are bound together by:
Your Answer: Adenine
Correct Answer: Hydrogen bonding.
Explanation:Nucleotides will always bind together via hydrogen bonds. There are two hydrogen bonds present between thymine and adenine and three hydrogen bonds present between guanine and cytosine.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 9
Incorrect
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The enzyme responsible for Telomeres to maintain their length after cell division is called:
Your Answer: None of the above telomeres shorten with all cell divisions
Correct Answer: Telomerase reverse transcriptase
Explanation:Telomeres are non-coding DNA consisting of repetitive nucleotide sequences plus proteins that are found at the end of the linear chromosomes. They maintain the integrity of the chromosomes and prevent their shortening.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 10
Incorrect
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Regarding DNA cloning and sequencing, all of the following are true, except:
Your Answer: Bacteriophages, viruses and plasmids are vectors
Correct Answer: Yeast artificial chromosomes ( yacs) are vectors
Explanation:Yeast chromosomes cannot be used as a vector. All the rest are true. Vectors can be bacteria, viruses and plasmids. DNA ligase binds the DNA fragment to the host DNA after insertion. Fluorescence can be used to visualize them.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 11
Incorrect
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With regards to P53, which statement is NOT true?
Your Answer: P53 plays a role in programmed cell death
Correct Answer: P53 is a RNA binding protein
Explanation:P53 is a tumour suppressor gene. It is not an RNA binding protein. It has been implicated in almost all tumours. It regulates the progression from G1 to the S phase of the cell cycle and is activated in response to damaged DNA.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 12
Incorrect
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Which of the following are true when it comes to tumour suppressor genes:
Your Answer: Mutation in the Rb gene leads to retinoblastoma
Correct Answer: All of the options are true
Explanation:All of the above mentioned statements are true regarding tumour suppressor genes. Tumour suppressor genes generally follow the two-hit hypothesis, which implies that both alleles that code for a particular protein must be affected before an effect is manifested.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 13
Incorrect
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Under normal conditions (where n represents the number of chromosome pairs), just before mitosis begins, how many chromosomes are contained in the nucleus of each somatic cell:
Your Answer: 0n
Correct Answer: 4n
Explanation:In a normal somatic cell there are 2n chromosome but in a replicating cell just before mitosis the chromosomes duplicate but are still joined via the centrosome. Thus there are 4n chromosomes. After completion of mitosis the number goes back to 2n.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 14
Incorrect
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In most somatic cells telomeres progressively shorten as:
Your Answer: Protein synthesis increases
Correct Answer: The cell divides
Explanation:Telomere length shortens with age. Progressive shortening of telomeres leads to senescence, apoptosis, or oncogenic transformation of somatic cells, affecting the health and lifespan of an individual. Telomeres prevent the chromosomes from shortening and prevent the coding portion of the DNA from being lost, thus allowing the cell to replicate indefinitely. During replication telomeres may be lost resulting in cell death.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 15
Incorrect
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Which of the following with regard to autosomal dominant disorders are true:
Your Answer: The offspring of a heterozygous individual has a 25% chance of inheriting the chromosome carrying the disease allele
Correct Answer: The offspring of a heterozygous individual has a 50% chance of inheriting the chromosome carrying the disease allele
Explanation:50% of the children will be effected from parents who are heterozygous for an autosomal dominant disorder. An allele can be dominant or recessive. Individuals, meanwhile, can be homozygous or heterozygous: individuals who are homozygous for a certain gene carry two copies of the same allele. individuals who are heterozygous for a certain gene carry two different alleles.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 16
Incorrect
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Which statement is incorrect regarding transcription of DNA?
Your Answer: Primary mRNA consists of both introns and exons.
Correct Answer: A gene is always read in the 3’-5’ orientation and at 3’ promoter sites.
Explanation:In both prokaryotes and eukaryotes RNA polymerase acts in the 5′-3′ direction and hence the RNA is transcribed in this direction. The mRNA produced is immature as it has introns as well as exons presents. It undergoes a process known as splicing to remove the exons and then interacts with the ribosomes to form proteins.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 17
Incorrect
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Normal parents have a child with a recessive condition, Tay Sachs. The chance of them having a normal child is?
Your Answer: 0%
Correct Answer: 75%
Explanation:The chance for normal parents having a child with a recessive disease is 1:4 or 25%. As both the parents are heterozygous for this condition. They have a 3:4 chance of having a normal child or 75%.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 18
Incorrect
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When during the cell cycle does DNA replication occur?
Your Answer: Cytokinesis
Correct Answer: S phase
Explanation:The S phase is known as the synthesis phase. During this phase DNA will begin to replicated, as well as the synthesis of the centrosomes and associated proteins.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 19
Incorrect
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In which phase do chromosomes in the nucleus become condensed into well-defined chromosomes?
Your Answer: Telophase
Correct Answer: Metaphase
Explanation:Prophase begins when the nucleus envelope disintegrates and the chromosomes start to condense. The chromosomes consist of two sister chromatids that are joined at a constriction known as centromere. When the cell reaches the metaphase the chromosomes are completely condensed and ready to align on the equatorial plate
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This question is part of the following fields:
- Genetics
- Medicine
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Question 20
Correct
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During which phase of the cell cycle does DNA synthesis occur?
Your Answer: S
Explanation:DNA synthesis occurs in the S phase of the cell cycle. In the G1 phase the cell prepares to divide. In G2 the cellular organelles divide and in the M phase mitosis occur. In the G0 phase the cell becomes quiescent and does not divide further
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This question is part of the following fields:
- Genetics
- Medicine
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Question 21
Incorrect
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In which phase do chromosomes in the nucleus become completely condensed into well-defined chromosomes?
Your Answer: Prophase
Correct Answer: Metaphase
Explanation:Prophase begins when the nucleus envelope disintegrates and the chromosomes start to condense. The chromosomes consist of two sister chromatids that are joined at a constriction known as centromere. When the cell reaches the metaphase the chromosomes are completely condensed and ready to align on the equatorial plate
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This question is part of the following fields:
- Genetics
- Medicine
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Question 22
Incorrect
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Which of the following is true for P53:
Your Answer: It binds e2f and stops the cell cycle at the g 1 phase
Correct Answer: It is induced by ‘broken’ DNA
Explanation:P53 gene is activated as a result of damaged DNA and if that cannot be repaired then it activates apoptosis.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 23
Incorrect
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Which of the following are true with regard to autosomal recessive disorders:
Your Answer: The offspring of an affected person will be heterozygotes unless other parent is also a carrier
Correct Answer: All are true
Explanation:All are true for autosomal recessive disorders.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 24
Incorrect
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Question 25
Incorrect
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Which of the following statements is true regarding chromosomes?
Your Answer: The centromere divides the chromosome into the long (q) and short (p) arms
Correct Answer: All are true
Explanation:All of the above mentioned statements are true regarding chromosomes.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 26
Correct
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Restriction Enzymes...
Your Answer: Cut DNA sequences at specific sites
Explanation:Restriction endonucleases are enzymes that recognise short sequences of double stranded DNA and cut them at specific nucleotide points or sequences. These sequences differ for different restriction endonucleases.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 27
Correct
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Telomerase is active in all of the following cells, except:
Your Answer: Certain liver cells
Explanation:Telomerase is an enzyme that adds repetitive nucleotide sequences to the ends of chromosomes (telomeres), preventing their shortening during cell division. Telomerase activity is crucial for cells that divide frequently and need to maintain their telomere length for continued proliferation. These include:
- Stem cells: They have high telomerase activity to maintain their long-term proliferative capacity.
- Germ cells: These cells also have active telomerase to ensure the stability of genetic material across generations.
- Certain white blood cells: Some immune cells, particularly those that need to proliferate in response to infection, show telomerase activity.
- Certain cancer cells: Many cancer cells reactivate telomerase, which contributes to their uncontrolled growth and immortality.
However, most somatic cells, including certain liver cells, do not exhibit significant telomerase activity. While some liver cells might show low levels of telomerase activity during regeneration, it is not generally active in normal, differentiated liver cells.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 28
Incorrect
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When one of the two copies of the autosomes has a mutation and the protein produced by the normal form of the gene cannot compensate. The affected individual has an:
Your Answer: X- linked recessive disorder
Correct Answer: Autosomal dominant disorder
Explanation:An autosomal dominant trait will be expressed no matter the consequence. If one chromosome has a mutation the other will not be able to compensate for the mutation hence the protein formed will be mutated and will not function properly.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 29
Incorrect
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Three adjacent nucleotides code for a particular amino acid. These are called codons. How many common amino acids are there and how many potential codon combinations make up the genetic code?
Your Answer:
Correct Answer: 20 amino acids, 64 codon combinations
Explanation:There are around 20 amino acids and 61 out of the 64 combinations of codon code for these 20 common amino acids.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 30
Incorrect
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Immortality can result from over expression of which enzyme?
Your Answer:
Correct Answer: Telomerase
Explanation:Telomerase activity is seen in germ cells and is absent in somatic cells. Telomeres prevent the chromosomes from shortening and prevent the coding portion of the DNA from being lost, thus allowing the cell to replicate indefinitely.
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This question is part of the following fields:
- Genetics
- Medicine
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