00
Correct
00
Incorrect
00 : 00 : 00
Session Time
00 : 00
Average Question Time ( Secs)
  • Question 1 - In most somatic cells telomeres progressively shorten as: ...

    Incorrect

    • In most somatic cells telomeres progressively shorten as:

      Your Answer: The host ages

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      9.7
      Seconds
  • Question 2 - 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: Chimerisation

      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
      23
      Seconds
  • Question 3 - What is the protective hexametric sequence at the ends of chromosomes called? ...

    Correct

    • What is the protective hexametric sequence at the ends of chromosomes called?

      Your Answer: Telomere

      Explanation:

      Telomeres are non coding DNA 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
      4.2
      Seconds
  • Question 4 - When 2 nucleotide chains of DNA bind together, thymine is bound to: ...

    Incorrect

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      20.2
      Seconds
  • Question 5 - The following cells replicate without shortening their telomeres because they express telomerase. ...

    Incorrect

    • The following cells replicate without shortening their telomeres because they express telomerase.

      Your Answer: Stem cells

      Correct 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      13.2
      Seconds
  • Question 6 - Regarding Southern Blotting and DNA probes, which answer is FALSE ...

    Incorrect

    • Regarding Southern Blotting and DNA probes, which answer is FALSE

      Your Answer:

      Correct Answer: RNA fragments are separated by gel electrophoresis and transferred onto membrane sheets in southern blotting

      Explanation:

      Restriction enzymes always cut at different positions. There are different restriction endonucleases for different nucleotide sequences.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds
  • Question 7 - Regarding restriction fragment length polymorphisms (RFLP) and Gene Knockout Mouse Models. All are...

    Incorrect

    • Regarding restriction fragment length polymorphisms (RFLP) and Gene Knockout Mouse Models. All are true except:

      Your Answer:

      Correct Answer: In knockout mouse models a gene is turned on through targeted mutation

      Explanation:

      In RFLP, polymorphism occurs in 98% of the non coding genome, resulting in no phenotypical change in the organism. A gene is not turned on by a mutation, rather the mutation at the restriction site will alter the DNA and the DNA will now form fragments of different lengths. PCR is a better technique than RFLP.

      A knockout, as related to genomics, refers to the use of genetic engineering to inactivate or remove one or more specific genes from an organism. Scientists create knockout organisms to study the impact of removing a gene from an organism, which often allows them to then learn something about that gene’s function.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      0
      Seconds
  • Question 8 - Which part of the chromosome plays a role in preserving its integrity and...

    Incorrect

    • Which part of the chromosome plays a role in preserving its integrity and stability?

      Your Answer:

      Correct Answer: Telomere

      Explanation:

      Telomeres are non coding DNA 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 9 - 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
  • Question 10 - 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:

      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
      0
      Seconds

SESSION STATS - PERFORMANCE PER SPECIALTY

Genetics (1/5) 20%
Medicine (1/5) 20%
Passmed