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  • Question 1 - During which phase of meiosis does exchange of genetic material occur accounting for...

    Correct

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

      Your 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
      8.4
      Seconds

  • Question 2 - In a knockout mouse model the process used to combine the new DNA...

    Correct

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

      Your 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
      6.7
      Seconds

  • Question 3 - Southern Blotting and DNA probes: ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      17.8
      Seconds

  • Question 4 - With regards to P53, which statement is NOT true? ...

    Incorrect

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      20.4
      Seconds

  • Question 5 - Consanguinity shows a strong association with which pattern of inheritance? ...

    Incorrect

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

      Your Answer: X linked recessive

      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
      10.2
      Seconds

  • Question 6 - Which of the following with regard to DNA mutations does not fit: ...

    Correct

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

      Your 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
      23.2
      Seconds

  • Question 7 - 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 dominant

      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
      82.7
      Seconds

  • Question 8 - In which phase do chromosomes in the nucleus become condensed into well-defined chromosomes?...

    Incorrect

    • In which phase do chromosomes in the nucleus become condensed into well-defined chromosomes?

      Your Answer: Telophase

      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
      9.4
      Seconds

  • Question 9 - Which statement about X linked dominant disorders is FALSE? ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      68.5
      Seconds

  • Question 10 - 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
      313.8
      Seconds

  • Question 11 - 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
      7.7
      Seconds

  • Question 12 - Which of the following with regard to autosomal dominant disorders are true: ...

    Correct

    • Which of the following with regard to autosomal dominant disorders are true:

      Your 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
      132.6
      Seconds

  • Question 13 - 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
      11.2
      Seconds

  • Question 14 - 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
      14.9
      Seconds

  • Question 15 - Which of the following is true for P 53: ...

    Correct

    • Which of the following is true for P 53:

      Your 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
      4.3
      Seconds

  • Question 16 - In which phase do chromosomes in the nucleus become completely condensed into well-defined...

    Correct

    • In which phase do chromosomes in the nucleus become completely condensed into well-defined chromosomes?

      Your 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
      13
      Seconds

  • Question 17 - Telomerase is active in the following cells except: ...

    Incorrect

    • Telomerase is active in the following cells except:

      Your Answer: Certain liver cells

      Correct Answer: Certain osteoblasts

      Explanation:

      Some cells have the ability to reverse telomere shortening by expressing telomerase, an enzyme that extends the telomeres of chromosomes. Telomerase is an RNA-dependent DNA polymerase, meaning an enzyme that can make DNA using RNA as a template.

      Telomerase is not usually active in most somatic cells (cells of the body), but it’s active in germ cells (the cells that make sperm and eggs) and some adult stem cells. These are cell types that need to undergo many divisions, or, in the case of germ cells, give rise to a new organism with its telomeric “clock” reset.
      Interestingly, many cancer cells have shortened telomeres, and telomerase is active in these cells. If telomerase could be inhibited by drugs as part of cancer therapy, their excess division (and thus, the growth of the cancerous tumor) could potentially be stopped.
       A subset of liver cells with high levels of telomerase renews the organ during normal cell turnover and after injury.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      14.2
      Seconds

  • Question 18 - Which of the following is true for P53: ...

    Correct

    • Which of the following is true for P53:

      Your 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
      10.7
      Seconds

  • Question 19 - Normal eukaryote somatic cells have: ...

    Correct

    • Normal eukaryote somatic cells have:

      Your Answer: 23 pairs of chromosomes

      Explanation:

      A normal somatic eukaryotic cell contains 46 chromosomes i.e. 23 pairs.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      11.9
      Seconds

  • Question 20 - During which phase are the 2 chromatids pulled apart at the centromere? ...

    Correct

    • During which phase are the 2 chromatids pulled apart at the centromere?

      Your Answer: Anaphase

      Explanation:

      During the prometaphase the microtubule organizing centre completely develops. The spindle fibers attach to the chromosome and the centriole. It is in the Anaphase however that the spindle fibers contract pulling the sister chromatids apart. Later in the anaphase a cleave furrow beings to forms.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      7.5
      Seconds

  • Question 21 - The process whereby DNA fragments are separated by size and charge is called:...

    Correct

    • The process whereby DNA fragments are separated by size and charge is called:

      Your Answer: Gel electrophoresis

      Explanation:

      Fragments of DNA of varying length can be separated on the basis of their charge and their size by a process called gel electrophoresis. Because DNA contains negatively charged phosphate groups, it will migrate in an electric field toward the positive electrode. Shorter chains migrate more rapidly through the pores of the gel, and thus separation depends on length. DNA bands in the gel can be visualized by various techniques including staining with dyes and autoradiography.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      4.9
      Seconds

  • Question 22 - Which of the following statements is true about chromosomes? ...

    Correct

    • Which of the following statements is true about chromosomes?

      Your 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
      20.5
      Seconds

  • Question 23 - Which statement is incorrect? ...

    Correct

    • Which statement is incorrect?

      Your Answer: Translation begins when the triplet (UGA) encoding for methionine is encountered.

      Explanation:

      Translation being when the codon for methionine is encountered which is AUG not UGA. This process is known as initiation. All the other options are correct.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      9.8
      Seconds

  • Question 24 - 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
      4.7
      Seconds

  • Question 25 - Mutation in RB can lead to the formation of which cancer? ...

    Correct

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

      Your 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
      2.9
      Seconds

  • Question 26 - Defects in chromosomal structure (and examples) include those mentioned below except: ...

    Correct

    • Defects in chromosomal structure (and examples) include those mentioned below except:

      Your Answer: Lyonization (x-linked disorders)

      Explanation:

      All are true except for A) Lyonization which is the inactivation of the X chromosomes in a female. It is not a chromosomal abnormality.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      9.5
      Seconds

  • Question 27 - Near the transcription site of a gene, the site at which RNA polymerase...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      5.6
      Seconds

  • Question 28 - 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
      21.3
      Seconds

  • Question 29 - The length of DNA is generally measured in terms of the number of:...

    Correct

    • The length of DNA is generally measured in terms of the 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
      3.4
      Seconds

  • Question 30 - When during the cell cycle do the centrioles replicate? ...

    Incorrect

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      87.4
      Seconds

  • Question 31 - Which of the following are true with regard to autosomal recessive disorders: ...

    Incorrect

    • Which of the following are true with regard to autosomal recessive disorders:

      Your Answer: These disorders are usually severe and many patients present in the first years of life and mortality is high

      Correct Answer: All are true

      Explanation:

      All are true for autosomal recessive disorders.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      61.3
      Seconds

  • Question 32 - In DNA cloning and sequencing, the bases in nucleotides chains are bound together...

    Correct

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

      Your 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
      6.1
      Seconds

  • Question 33 - Telomeres are best described as: ...

    Correct

    • Telomeres are best described as:

      Your 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      8.9
      Seconds

  • Question 34 - Immortality can result from over expression of which enzyme? ...

    Correct

    • 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      20.3
      Seconds

  • Question 35 - Which of the following statements is not true about mitochondrial chromosomes? ...

    Correct

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

      Your 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
      39.3
      Seconds

  • Question 36 - Regarding Southern Blotting and DNA probes, which answer is FALSE ...

    Correct

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

      Your 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
      22.5
      Seconds

  • Question 37 - During which stage does the mitotic apparatus dissolute? ...

    Correct

    • During which stage does the mitotic apparatus dissolute?

      Your 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
      9.5
      Seconds

  • Question 38 - 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
      11.3
      Seconds

  • Question 39 - Which statement is correct regarding mRNA? ...

    Incorrect

    • Which statement is correct regarding mRNA?

      Your Answer: The bases of mRNA consists of adenine, guanine, cytosine and thymine.

      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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      21.4
      Seconds

  • Question 40 - Regarding DNA cloning and sequencing, all of the following are true, except: ...

    Incorrect

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

      Your Answer: In sequencing dideoxysequencing allows identification of exact nucleotide sequence

      Correct 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
      40.7
      Seconds

  • Question 41 - In most somatic cells telomeres progressively shorten as: ...

    Correct

    • In most somatic cells telomeres progressively shorten as:

      Your 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
      3.3
      Seconds

  • Question 42 - 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
      34.3
      Seconds

  • Question 43 - The enzyme responsible for Telomeres to maintain their length after cell division is...

    Correct

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

      Your 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
      37.5
      Seconds

  • Question 44 - When during the cell cycle does DNA replication occur? ...

    Correct

    • When during the cell cycle does DNA replication occur?

      Your 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.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      8.8
      Seconds

  • Question 45 - Which of the following is an incorrect statement regarding the structure of DNA?...

    Correct

    • Which of the following is an incorrect statement regarding the structure of DNA?

      Your Answer: The two strands of DNA are held together by cysteine bonds.

      Explanation:

      The two strands of DNA are held together by hydrogen bonds formed between the nucleotide bases.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      29.6
      Seconds

  • Question 46 - Which of the following is not true regarding mitochondrial chromosome disorders? ...

    Correct

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

      Your Answer: Because mitochondrial chromosomes have no introns in their genes, any point mutation has a low likelihood of having an effect.

      Explanation:

      Any point mutation in any part of the mitochondrial DNA will lead to a mutated mitochondria and will likewise have its ill effect on the body.

    • This question is part of the following fields:

      • Genetics
      • Medicine
      73.7
      Seconds

  • Question 47 - 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
      4
      Seconds

  • Question 48 - 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: Intron

      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
      10.5
      Seconds

  • Question 49 - 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: 12 amino acids, 24 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
      48
      Seconds

  • Question 50 - 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

SESSION STATS - PERFORMANCE PER SPECIALTY

Genetics (39/49) 80%
Medicine (39/49) 80%
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