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  • Question 1 - Restriction Enzymes... ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      28.4
      Seconds
  • Question 2 - The chromosomes that principally encode for proteins or RNA molecules involved in mitochondrial...

    Incorrect

    • The chromosomes that principally encode for proteins or RNA molecules involved in mitochondrial function are found:

      Your Answer: In the mitochondria of the cell

      Correct Answer: In the nucleus of each diploid cell

      Explanation:

      While mitochondria have their own small circular DNA (mtDNA) that encodes some of the proteins and RNAs required for mitochondrial function, the majority of proteins involved in mitochondrial function are encoded by nuclear DNA. These nuclear genes are transcribed in the nucleus and then translated into proteins in the cytoplasm. The proteins are subsequently imported into the mitochondria.

      Therefore, the correct answer is:

      • In the nucleus of each diploid cell

    • This question is part of the following fields:

      • Genetics
      • Medicine
      34.1
      Seconds
  • Question 3 - At the end of which phase will P53 halt the cell cycle? ...

    Correct

    • At the end of which phase will P53 halt the cell cycle?

      Your Answer: G1 phase

      Explanation:

      P53 regulates the cell cycle. It regulates the progression from G1 to S phase

    • This question is part of the following fields:

      • Genetics
      • Medicine
      54.3
      Seconds
  • Question 4 - In which phase do chromosomes in the nucleus become completely condensed into well-defined...

    Incorrect

    • 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

    • This question is part of the following fields:

      • Genetics
      • Medicine
      108.9
      Seconds
  • Question 5 - Which of the following with regard to autosomal dominant disorders are true: ...

    Incorrect

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      117.1
      Seconds
  • Question 6 - 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
      107
      Seconds
  • Question 7 - Which of the following is true for P 53: ...

    Incorrect

    • Which of the following is true for P 53:

      Your Answer: It is induced by histone deacetylase protein

      Correct Answer: It is induced by ‘broken’ DNA

      Explanation:

      All of the above mentioned statements are true regarding tumour suppressor genes.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      14.8
      Seconds
  • Question 8 - 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: Hydrogen bonds

      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
      15
      Seconds
  • Question 9 - Regarding Gene Knockout Mouse Models, all are true except: ...

    Incorrect

    • Regarding Gene Knockout Mouse Models, all are true except:

      Your Answer: RFLP can be sub categorised as slp( single locus proband mlp( multi locus probe).

      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).

    • This question is part of the following fields:

      • Genetics
      • Medicine
      66.1
      Seconds
  • Question 10 - Which statement is correct? ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      41
      Seconds
  • Question 11 - With regard to X linked disorders which of the following are true ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      85.2
      Seconds
  • Question 12 - The length of DNA is generally measured in terms of number of: ...

    Correct

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

      Your 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
      20.3
      Seconds
  • Question 13 - In most somatic cells telomeres progressively shorten as: ...

    Incorrect

    • In most somatic cells telomeres progressively shorten as:

      Your Answer: None of the above

      Correct Answer: The cell divides

      Explanation:

      Telomerase activity is seen in germ cells and is absent in somatic cells. A somatic cell is any biological cell forming the body of an organism, other than a gamete, germ cell, gametocyte or undifferentiated stem cell. i.e. liver 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
      22.8
      Seconds
  • Question 14 - Which of the following is true for P53: ...

    Incorrect

    • Which of the following is true for P53:

      Your Answer: Induction will induce necrosis in cancerous cells

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      12.9
      Seconds
  • Question 15 - 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: X linked recessive

      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
      78.8
      Seconds
  • Question 16 - In DNA cloning and sequencing, the bases in nucleotides chains are bound together...

    Incorrect

    • In DNA cloning and sequencing, the bases in nucleotides chains are bound together by:

      Your Answer: Histones

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      17.5
      Seconds
  • Question 17 - In most somatic cells telomeres progressively shorten as: ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      42.2
      Seconds
  • Question 18 - Southern Blotting and DNA probes: ...

    Incorrect

    • Southern Blotting and DNA probes:

      Your Answer: Gene probes can be labelled with radioactive isotopes e.g. 32 p

      Correct 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      8
      Seconds
  • Question 19 - Critical shortening of Telomeres result in: ...

    Correct

    • 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

    • This question is part of the following fields:

      • Genetics
      • Medicine
      12.8
      Seconds
  • Question 20 - In RFLP (restriction fragment length polymorphism), the DNA fragments are separated by length...

    Incorrect

    • In RFLP (restriction fragment length polymorphism), the DNA fragments are separated by length through a process known as:

      Your Answer: Insertion

      Correct 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
      12.7
      Seconds
  • Question 21 - Regarding DNA cloning and sequencing, all of the following are true, except: ...

    Correct

    • Regarding DNA cloning and sequencing, all of the following are true, except:

      Your 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      19.3
      Seconds
  • Question 22 - During which phase of the cell cycle does transcription of DNA synthesis molecules...

    Incorrect

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

      Your Answer: G2

      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.

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      10.2
      Seconds
  • Question 23 - Which of the following statements is true about chromosomes? ...

    Incorrect

    • Which of the following statements is true about chromosomes?

      Your Answer: Diploid human cells have 46 chromosomes, 23 inherited from each parent

      Correct Answer: All of the above

      Explanation:

      All of the above mentioned statements are true regarding chromosomes.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      87.8
      Seconds
  • Question 24 - Which of the following with regard to DNA mutations does not fit: ...

    Incorrect

    • Which of the following with regard to DNA mutations does not fit:

      Your Answer: Point mutations are the simplest type of change and may or may not cause a clinical disorder

      Correct Answer: All gene mutations cause clinical disease entities

      Explanation:

      All gene mutations do not cause a clinical manifestation of the disease, some gene mutations are silent mutations. They are present but do not cause any disease.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      72.2
      Seconds
  • Question 25 - In Restriction Fragment Length Polymorphism (RFLP), the DNA fragments are separated by length through...

    Incorrect

    • In Restriction Fragment Length Polymorphism (RFLP), the DNA fragments are separated by length through a process known as:

      Your Answer: Inversion

      Correct 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      49.8
      Seconds
  • Question 26 - Which statement is correct regarding mRNA? ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      17.8
      Seconds
  • Question 27 - 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: Osteosarcoma

      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
      16.2
      Seconds
  • Question 28 - 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: Knockout models are important in studying roles of sequenced genes with unknown function

      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
      38.2
      Seconds
  • Question 29 - 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: 5th end

      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
      26.2
      Seconds
  • Question 30 - With regard to X-linked disorders which of the following are true: ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      19.4
      Seconds

SESSION STATS - PERFORMANCE PER SPECIALTY

Genetics (10/30) 33%
Medicine (10/30) 33%
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