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Question 1
Correct
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Immortality can result from over expression of which enzyme?
Your 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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Question 2
Incorrect
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In meiosis, the period of prophase 1 involves:
Your Answer: Chromosomes aligning themselves on the microtubules at the centre of the cell
Correct Answer: Replicated DNA condensing to form visible chromosomes
Explanation:Prophase 1 has been divided into five different stages (laptotene, zygotene, pachytene, diplotene and diakinesis). In prophase 1, chromosomes are going to condense to become visible, each chromosome will contain two chromatids that are joined at the centromere.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 3
Correct
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Southern Blotting and DNA probes:
Your Answer: DNA fragments are separated by gel electrophoresis and transferred onto membrane sheets in 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 4
Incorrect
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Regarding Gene Knockout Mouse Models, all are true except:
Your Answer: RFLP analysis is slow and cumbersome and is now largely obsolete
Correct Answer: In knockout mouse models a gene is turned on through targeted mutation
Explanation:In knockout mouse models, a gene is not turned on but rather turned off or “knocked out” through targeted mutation. This involves disrupting or deleting the gene to study the effects of its loss of function. Knockout models are crucial for understanding the roles of specific genes, particularly those with unknown functions.
The other statements are true:
- Knockout models are important in studying the roles of sequenced genes with unknown function.
- RFLP (Restriction Fragment Length Polymorphisms) can be subcategorized as SLP (single locus probe) and MLP (multi locus probe).
- RFLP analysis is slow and cumbersome and is now largely obsolete, having been replaced by more efficient techniques.
- Sequence changes involved in RFLP can be analyzed more quickly by PCR (Polymerase Chain Reaction).
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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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Near the transcription site of a gene, the site at which RNA polymerase and its cofactors bind is known as the:
Your Answer: Activator
Correct 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 6
Incorrect
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Carcinogens found in cigarette smoke can transform proto-oncogenes to oncogenes through:
Your Answer: Mutations in p53
Correct Answer: Point mutations in genomic DNA
Explanation:80% of the pancreatic cancers are environmentally influenced by smoking which increases the risk by 50%. Mutation can occur in the KRAS, p16, SMAD4, and TP53 genes among other tumour suppression genes. Smoking can be implicated in transformation of all these genes. Apart from KRAS all the genes are inactivated in pancreatic cancer. As KRAS is the most commonly altered gene, mutation occurs as point mutation. As smoking is the most common aetiology in pancreatic cancer, and KRAS is the most important gene that is altered. Most commonly cigarette smoke causes point mutation.
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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
Correct
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Question 9
Correct
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Which statement is correct regarding mRNA?
Your 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 10
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 11
Correct
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Question 12
Correct
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In RFLP (restriction fragment length polymorphism), the DNA fragments are separated by length through a process known as:
Your Answer: Agarose 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 13
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 14
Correct
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Which statement about X linked dominant disorders is FALSE?
Your Answer: Heterozygous females tend to have the disease more severely than affected males.
Explanation:Women who have the affected X chromosome will be affected, but the severity will be less than that in males as they have a normal X chromosome to counter the effect of the mutated X chromosome. Affected males will pass on the defect to their daughters 100% of the time but not to their sons.
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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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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: 2n
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 16
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: Krebs cycle
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 17
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: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 18
Incorrect
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Which of the following statements is not true about mitochondrial chromosomes?
Your Answer: Are mainly inherited from the mother
Correct Answer: Mitochondrial chromosomes play no role in the transmission of disease from generation to generation.
Explanation:All the above mentioned statements are true except that mitochondrial DNA is passed from the mother to the child. If the child inherits the defective mitochondrial gene it will manifest some form of the disease. Commonly inherited diseases related to mitochondrial abnormality are Leber hereditary optic neuropathy and myoclonic epilepsy with ragged red fibers (MERRF).
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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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With regard to X linked disorders which of the following are true
Your Answer: None of the above
Correct 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 20
Incorrect
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Which statement is incorrect regarding transcription of DNA?
Your Answer: Only two AT-rich promoter sites are present in eukaryotic cells, i.e. TATA box and CAAT box.
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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SESSION STATS - PERFORMANCE PER SPECIALTY
