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Question 1
Correct
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In Restriction Fragment Length Polymorphism (RFLP), the DNA fragments are separated by length through a process known as:
Your Answer: Gel electrophoresis
Explanation:Samples of DNA from individuals are broken into pieces by restriction enzymes and the fragments are separated according to their lengths via gel electrophoresis. Although now largely obsolete due to the rise of inexpensive DNA sequencing technologies, RFLP analysis was the first DNA profiling technique inexpensive enough to see widespread application.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 2
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 3
Incorrect
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Which of the following conditions is NOT X-linked recessive?
Your Answer: Duchenne muscular dystrophy
Correct Answer: Cystic fibrosis
Explanation:Cystic fibrosis is a autosomal recessive disease with an incidence of about 1 in 2500 live births. The most common mutation occurs in the long arm of chromosome 7 which codes for the chloride channel (cystic fibrosis transmembrane conductance regulator) gene.
To have CF, a child must inherit two abnormal genes—one from each parent. The recessive CF gene can occur in both boys and girls because it is located on non-sex-linked chromosomes called autosomal chromosomes.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 4
Correct
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Near the transcription site of a gene, the site at which RNA polymerase and its cofactors bind is known as the:
Your Answer: Promotor
Explanation:Transcription will begin when the RNA polymerase II binds to the promotor. The promotor is a sequence of 25 nucleotides found upstream from the start site of transcription. This promotor sequence is known as the TATA box. Transcription factors also bond along with RNA polymerase to this site to form a complex. However some may bind to regulatory elements proximal to the promotor site.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 5
Correct
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Question 6
Incorrect
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Telomeres are best described as:
Your Answer: A complex repetitive glycoprotein structure at the end point of DNA protecting the DNA from damage.
Correct Answer: A repetitive DNA sequence at the end of a DNA molecule.
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 7
Incorrect
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Which of the following is not true regarding mitochondrial chromosome disorders?
Your Answer: Retinal degeneration, diabetes mellitus and some forms of hearing loss are some of the other disease attributed to mitochondrial chromosome defects
Correct Answer: Because mitochondrial chromosomes have no introns in their genes, any point mutation has a low likelihood of having an effect.
Explanation:Mitochondrial DNA (mtDNA) does indeed lack introns, meaning that its genes are closely packed with coding sequences. This actually means that any point mutation in the mtDNA is more likely to have an effect, not less. The lack of introns means there are fewer non-coding regions where mutations can occur without affecting gene function. Thus, mutations in mtDNA often have significant consequences because they are more likely to alter essential coding sequences.
The other statements are true:
- Most mitochondrial diseases are myopathies and neuropathies with a maternal pattern of inheritance: This is correct because mtDNA is inherited maternally, and many mitochondrial disorders affect muscle and nerve function.
- Retinal degeneration, diabetes mellitus, and some forms of hearing loss are some of the other diseases attributed to mitochondrial chromosome defects: These are indeed conditions associated with mitochondrial defects.
- Mitochondrial chromosome defects are inherited from one’s mother: This is correct, as mtDNA is passed from mother to offspring.
- Leber’s hereditary optic neuropathy (LHON), the commonest cause of blindness in young men, is an example of a mitochondrial chromosome defect: This is true; LHON is a well-known mitochondrial disorder.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 8
Correct
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Critical shortening of Telomeres result in:
Your Answer: Activation of p53 and prb and cell crisis
Explanation:Telomeres are repetitive nucleotide sequences at the ends of chromosomes that protect them from deterioration or from fusion with neighboring chromosomes. Each time a cell divides, its telomeres shorten. When they become critically short, they can no longer protect the chromosome ends, triggering a DNA damage response.
This response leads to the activation of tumor suppressor proteins p53 and pRb (retinoblastoma protein). Activated p53 can induce cell cycle arrest, allowing time for DNA repair or triggering apoptosis if the damage is irreparable. Similarly, pRb helps regulate cell cycle progression and can halt the cell cycle to prevent the proliferation of cells with damaged DNA.
As a result, the cell enters a state of crisis, characterized by widespread cell death and genomic instability, which ultimately prevents the propagation of cells with critically shortened telomeres.
Therefore, the correct answer is:
Activation of p53 and pRb and cell crisis
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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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In a knockout mouse model the process used to combine the new DNA sequence and the stem cells is known as:
Your Answer: Recombination
Correct Answer: Insertion
Explanation:Chimerisation is also known as the formation of recombinant DNA. When a foreign DNA sequence is inserted into a plasmid or other DNA sequence, this process is known as insertion.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 10
Correct
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In most somatic cells telomeres progressively shorten as:
Your 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 11
Correct
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Which of the following is false with regard to the following statement: Proto- oncogenes can be transformed to oncogenes in the following ways.
Your Answer: Inhibition of P53
Explanation:Proto oncogenes cannot be transformed into oncogenes due to inhibition of P53 gene. There has to be a mutation in the proto oncogene. All the other options are true.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 12
Correct
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With regard to X linked disorders which of the following are true
Your Answer: X linked recessive disorders usually present in males and only very rarely present in homozygous females
Explanation:All are true for autosomal recessive disorders. Dominance rules for sex-linked gene loci are determined by their behaviour in the female: because the male has only one allele (except in the case of certain types of Y chromosome aneuploidy), that allele is always expressed regardless of whether it is dominant or recessive.
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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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With regards to P53, which statement is NOT true?
Your Answer: P53’s own expression is induced by broken DNA
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 14
Correct
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The following cells replicate without shortening their telomeres because they express telomerase.
Your Answer: Germ cells
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. 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
Correct
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Consanguinity shows a strong association with which pattern of inheritance?
Your Answer: Autosomal recessive
Explanation:Consanguinity involves being from the same kinship as another person. It is a common feature of an autosomal recessive mode of inheritance
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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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Male to male transmission is a key factor of which type of inheritance?
Your Answer: None of the above
Correct 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 17
Incorrect
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Which statement is correct regarding mRNA?
Your Answer: mRNA is double stranded and acts as a template for protein synthesis.
Correct Answer: mRNAs are mainly found in the nucleus and cytoplasm of a cell.
Explanation:mRNA is transcribed from DNA and is carried to the cytosol to be translated. Hence it is mainly found in the cytosol and the nucleus of a cell. It is single stranded and contains the base uracil instead of thymine.
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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: G1 phase
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
Correct
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During which phase of the cell cycle does transcription of DNA synthesis molecules 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.
Interphase is composed of G1 phase (cell growth), followed by S phase (DNA synthesis), followed by G2 phase (cell growth). At the end of interphase comes the mitotic phase, which is made up of mitosis and cytokinesis and leads to the formation of two daughter cells.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 20
Incorrect
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The mitochondrial chromosome is a circular DNA molecule. They encode for proteins needed for ATP production. These proteins are also essential for:
Your Answer: Oxidative phosphorylation
Correct Answer: Apoptotic cell death
Explanation:The intrinsic pathway or the mitochondrial pathway of apoptosis is activated due to the loss of BCL-2 and other antiapoptotic proteins. This loss results in the increased membrane permeability and release of cytochrome C which activates caspases downstream resulting in apoptosis.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 21
Correct
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With regard to X-linked disorders which of the following are true:
Your Answer: X linked recessive disorders usually present in males and only very rarely present in homozygous females
Explanation:X linked disorders are more common in males as they only need one mutated copy of the X chromosome to manifest the disease with full severity while the females need two X chromosomes to manifest the disease, even with one defected X chromosome the severity is less than that seen in males.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 22
Correct
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The process by which DNA fragments are separated by gel and transferred onto a membrane sheet is called:
Your Answer: Southern blotting
Explanation:A Southern blot is a method used in molecular biology for detection of a specific DNA sequence in DNA samples. Southern blotting combines transfer of electrophoresis-separated DNA fragments to a filter membrane and subsequent fragment detection by probe hybridization. The other forms of blotting involve the use of RNA and proteins.
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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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When during the cell cycle do the centrioles replicate?
Your Answer: Mitosis
Correct Answer: G1 phase
Explanation:During G1 phase the cell will prepare for cell division. All the organelles will start to duplicate in this phase and the cell will begin to grow whilst proteins are also synthesized.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 24
Correct
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Question 25
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 26
Correct
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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: 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 27
Correct
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Which statement is correct?
Your Answer: MtDNA principally encodes for proteins that are involved in oxidative phosphorylation for the production of ATP in the cell.
Explanation:Mitochondria have no nucleus instead they contain their own free floating circular genome (MtDNA), which encodes 13 different subunits of proteins involved in oxidative phosphorylation. The remainder of the mitochondrial proteins are nuclear encoded, synthesized in the cytoplasm, and transported into the mitochondria.
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This question is part of the following fields:
- Genetics
- Medicine
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SESSION STATS - PERFORMANCE PER SPECIALTY
