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  • Question 1 - When one of the two copies of the autosomes has a mutation and...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      14.2
      Seconds

  • Question 2 - The process of DNA amplification and quantification is called: ...

    Correct

    • The process of DNA amplification and quantification is called:

      Your Answer: PCR

      Explanation:

      PCR/polymerase chain reaction is a procedure carried out in a test tube that can be used on the smallest amount of DNA to amplify it, allowing for millions of copies of specific nucleotides to be made.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      12.7
      Seconds

  • Question 3 - Three adjacent nucleotides code for a particular amino acid. These are called codons....

    Incorrect

    • 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: 156 amino acids, 156 codon combinations

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      759.1
      Seconds

  • Question 4 - In RFLP (restriction fragment length polymorphism), the DNA fragments are separated by length...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      8.3
      Seconds

  • Question 5 - Which of the following is false with regard to the following statement: Proto-...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      7.5
      Seconds

  • Question 6 - Regarding Polymerase Chain Reaction, all are true except: ...

    Incorrect

    • Regarding Polymerase Chain Reaction, all are true except:

      Your Answer: Is an in vitro technique

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      13.8
      Seconds

  • Question 7 - The process by which DNA fragments are separated by gel and transferred onto...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      5.7
      Seconds

  • Question 8 - Carcinogens found in cigarette smoke can transform proto-oncogenes to oncogenes through: ...

    Incorrect

    • Carcinogens found in cigarette smoke can transform proto-oncogenes to oncogenes through:

      Your Answer: Inhibiting tumour suppressor genes.

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      8.2
      Seconds

  • Question 9 - During which phase of meiosis does exchange of genetic material occur accounting for...

    Incorrect

    • During which phase of meiosis does exchange of genetic material occur accounting for genetic diversity between individuals:

      Your Answer:

      Correct Answer: Prophase 1

      Explanation:

      Prophase 1 has been divided into five different stages ( laptotene, zygotene, pachytene, diplotene ans diakinesis). In prophase 1 chromosomes are going to condense to become visible, each chromosome will contain two chromatids that are joined at the centromere. the nucleolus and nuclear envelope are going to disintegrate. the homologous chromosomes will form tetrad and crossing over will occur between the chromosomes (random exchange of genes), the point of exchange is known as the chiasmata, this increases genetic diversity.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 10 - In a knockout mouse model the process used to combine the new DNA...

    Incorrect

    • In a knockout mouse model the process used to combine the new DNA sequence and the stem cells is known as:

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 11 - Immortality can result from over expression of which enzyme? ...

    Incorrect

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 12 - With regards to P53, which statement is NOT true? ...

    Incorrect

    • With regards to P53, which statement is NOT true?

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 13 - The enzyme responsible for Telomeres to maintain their length after cell division is...

    Incorrect

    • The enzyme responsible for Telomeres to maintain their length after cell division is called:

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 14 - When during the cell cycle do the centrioles replicate? ...

    Incorrect

    • When during the cell cycle do the centrioles replicate?

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 15 - Which of the following are true when it comes to tumour suppressor genes:...

    Incorrect

    • Which of the following are true when it comes to tumour suppressor genes:

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 16 - Male to male transmission is a key factor of which type of inheritance?...

    Incorrect

    • Male to male transmission is a key factor of which type of inheritance?

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 17 - During which stage does the mitotic apparatus dissolute? ...

    Incorrect

    • During which stage does the mitotic apparatus dissolute?

      Your Answer:

      Correct Answer: Telophase

      Explanation:

      In telophase the nuclear envelope along with the nucleolus will reappear. The daughter nuclei will enlarge as the chromosome will decondense again. Along with this, cytokinesis will occur. At the end of cytokinesis the daughter centrioles will move from the poles to the intercellular bridge where they will be disassembled and complete the separation of the daughter cells

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 18 - During which phase of the cell cycle does DNA synthesis occur? ...

    Incorrect

    • During which phase of the cell cycle does DNA synthesis occur?

      Your Answer:

      Correct 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

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 19 - Which of the following statements is not true about mitochondrial chromosomes? ...

    Incorrect

    • Which of the following statements is not true about mitochondrial chromosomes?

      Your Answer:

      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).

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 20 - Mutation in RB can lead to the formation of which cancer? ...

    Incorrect

    • Mutation in RB can lead to the formation of which cancer?

      Your Answer:

      Correct Answer: Retinoblastoma

      Explanation:

      Patients with a history of autosomal dominant familial retinoblastoma have at least one mutated copy of the RB gene. This predisposes the patient to develop retinoblastoma in one or both the eyes. Patients with a family history should be screened properly so that it can be detected and treated as early as possible.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 21 - Which of the following conditions results from chromosomal ‘non-disjunction’? ...

    Incorrect

    • Which of the following conditions results from chromosomal ‘non-disjunction’?

      Your Answer:

      Correct Answer: All of the options

      Explanation:

      Non-disjunction can result in aneuploidy i.e. abnormal number of chromosomes in a cell. It results due to uneven division of chromosomes in the meiosis 1 or 2 phase. All the above mentioned examples are of non-disjunction.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 22 - The telomerase is capable of adding several more repeats of telomeres at which...

    Incorrect

    • The telomerase is capable of adding several more repeats of telomeres at which end of the guanosine rich region.

      Your Answer:

      Correct Answer: 3rd end

      Explanation:

      Telomerase is a reverse transcriptase that uses the RNA template to synthesize DNA in the 5th-3rd direction resulting in extension of the 3rd end and then translocates it to the newly synthesized end. The GT rich strand is thus elongated.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 23 - Which of the following is not true regarding mitochondrial chromosome disorders? ...

    Incorrect

    • Which of the following is not true regarding mitochondrial chromosome disorders?

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 24 - Consanguinity shows a strong association with which pattern of inheritance? ...

    Incorrect

    • Consanguinity shows a strong association with which pattern of inheritance?

      Your Answer:

      Correct 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

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 25 - The mitochondrial chromosome is a circular DNA molecule. They encode for proteins needed...

    Incorrect

    • The mitochondrial chromosome is a circular DNA molecule. They encode for proteins needed for ATP production. These proteins are also essential for:

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 26 - Which statement is incorrect regarding transcription of DNA? ...

    Incorrect

    • Which statement is incorrect regarding transcription of DNA?

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 27 - Which statement is correct? ...

    Incorrect

    • Which statement is correct?

      Your Answer:

      Correct 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 28 - The length of DNA is generally measured in terms of the number of:...

    Incorrect

    • The length of DNA is generally measured in terms of the number of:

      Your Answer:

      Correct Answer: Base pairs

      Explanation:

      As DNA is made up of nucleotides, its length is measured by the number of base pairs in the DNA molecules.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 29 - Near the transcription site of a gene, the site at which RNA polymerase...

    Incorrect

    • Near the transcription site of a gene, the site at which RNA polymerase and its cofactors bind is known as the:

      Your Answer:

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

  • Question 30 - With regard to X-linked disorders which of the following are true: ...

    Incorrect

    • With regard to X-linked disorders which of the following are true:

      Your Answer:

      Correct 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds

SESSION STATS - PERFORMANCE PER SPECIALTY

Genetics (5/8) 63%
Medicine (5/8) 63%
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