-
Question 1
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
-
-
Question 2
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
-
-
Question 3
Correct
-
Question 4
Incorrect
-
Which of the following are true with regard to autosomal recessive disorders:
Your Answer: These disorders only manifest themselves where an individual is homozygous for the disease allele
Correct Answer: All are true
Explanation:All are true for autosomal recessive disorders.
-
This question is part of the following fields:
- Genetics
- Medicine
-
-
Question 5
Correct
-
Question 6
Correct
-
Which of the following conditions results from chromosomal ‘non-disjunction’?
Your 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
-
-
Question 7
Incorrect
-
Telomerase is active in the following cells except:
Your Answer: Certain cancer 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
-
-
Question 8
Correct
-
In which stage of mitosis are the chromosomes most obvious or prominent?
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
-
-
Question 9
Incorrect
-
In which phase do chromosomes in the nucleus become completely condensed into well-defined chromosomes?
Your Answer: Prometaphase
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
-
-
Question 10
Correct
-
Question 11
Correct
-
Question 12
Correct
-
In Restriction Fragment Length Polymorphism (RFLP), the DNA fragments are separated by length through a process known as:
Your 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
-
-
Question 13
Incorrect
-
Regarding Polymerase Chain Reaction, all are true except:
Your Answer: DNA polymerase extends primers using target DNA as template
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
-
-
Question 14
Incorrect
-
In most somatic cells telomeres progressively shorten as:
Your Answer: The cell 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
-
-
Question 15
Incorrect
-
During which phase of meiosis does exchange of genetic material occur accounting for genetic diversity between individuals:
Your Answer: Telophase 2
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
-
-
Question 16
Incorrect
-
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: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
-
-
Question 17
Incorrect
-
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.
-
This question is part of the following fields:
- Genetics
- Medicine
-
-
Question 18
Incorrect
-
Regarding restriction fragment length polymorphisms (RFLP) and Gene Knockout Mouse Models. All are true except:
Your Answer: Sequence changes involved in RFLP can be analysed more quickly by PCR.
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
-
-
Question 19
Incorrect
-
With regards to P53, which statement is NOT true?
Your Answer: P53 activates many gene expression pathways
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
-
-
Question 20
Incorrect
-
Telomerase is active in all of the following cells, except:
Your Answer: Certain osteoblasts
Correct Answer: Certain liver cells
Explanation:Telomerase is an enzyme that adds repetitive nucleotide sequences to the ends of chromosomes (telomeres), preventing their shortening during cell division. Telomerase activity is crucial for cells that divide frequently and need to maintain their telomere length for continued proliferation. These include:
- Stem cells: They have high telomerase activity to maintain their long-term proliferative capacity.
- Germ cells: These cells also have active telomerase to ensure the stability of genetic material across generations.
- Certain white blood cells: Some immune cells, particularly those that need to proliferate in response to infection, show telomerase activity.
- Certain cancer cells: Many cancer cells reactivate telomerase, which contributes to their uncontrolled growth and immortality.
However, most somatic cells, including certain liver cells, do not exhibit significant telomerase activity. While some liver cells might show low levels of telomerase activity during regeneration, it is not generally active in normal, differentiated liver cells.
-
This question is part of the following fields:
- Genetics
- Medicine
-
-
Question 21
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
-
-
Question 22
Correct
-
Question 23
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
-
-
Question 24
Correct
-
Question 25
Correct
-
The process where by 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
-
-
Question 26
Correct
-
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: 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
-
-
Question 27
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
-
-
Question 28
Incorrect
-
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.
-
This question is part of the following fields:
- Genetics
- Medicine
-
-
Question 29
Incorrect
-
The chromosomes that principally encode for proteins or RNA molecules involved in mitochondrial function are found:
Your Answer: In the nucleolus of each diploid 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
-
-
Question 30
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
-
SESSION STATS - PERFORMANCE PER SPECIALTY
