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Question 1
Incorrect
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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
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Question 2
Incorrect
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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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 3
Incorrect
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Which statement is incorrect?
Your Answer: AAUAAA acts as a cleavage signal for endonucleases.
Correct 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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 4
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 5
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 6
Correct
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Question 7
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 8
Correct
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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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 9
Incorrect
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 10
Incorrect
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The process by which RNA fragments are separated by gel electrophoresis and transferred onto a membrane sheet is called:
Your Answer: Southern blotting
Correct Answer: Northern blotting
Explanation:Blots of the gel can be made from using nitrocellulose paper. Northern blots are produced when a fragment of radioactive DNA hybridize with RNA on a nitrocellulose blot of a gel and southern blots are produced when DNA hybrize with DNA on a nitrocellulose blot of the gel.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 11
Incorrect
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In which stage of mitosis are the chromosomes most obvious or prominent?
Your Answer: G1 phase
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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 12
Correct
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In meiosis, the period of prophase 1 involves:
Your Answer: Replicated DNA condensing to form visible chromosomes
Explanation:Prophase 1 has been divided into five different stages (laptotene, zygotene, pachytene, diplotene and diakinesis). In prophase 1, chromosomes are going to condense to become visible, each chromosome will contain two chromatids that are joined at the centromere.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 13
Incorrect
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Which of the following with regard to autosomal dominant disorders are true:
Your Answer: The offspring of a heterozygous individual has a 75% 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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 14
Incorrect
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The enzyme responsible for Telomeres to maintain their length after cell division is called:
Your Answer: Telomere transcriptase
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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 15
Correct
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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).
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This question is part of the following fields:
- Genetics
- Medicine
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Question 16
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 17
Correct
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What is the role of cyclin and cyklin-dependent kinases in mitosis:
Your Answer: Phosphorylation of proteins that make up pre-replication complexes
Explanation:There are certain regulators of the cell cycles that mediate progression through the cell cycle. These are cyclins and cyklin-dependent kinases (CDKs). They form a complex that phosphorylates protein involved in the cell cycle.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 18
Incorrect
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 19
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 20
Correct
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Question 21
Incorrect
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What is the structure of nucleosomes?
Your Answer: Strands of single strand DNA + histones
Correct Answer: Strands of double strand DNA + histones
Explanation:DNA is packed and condensed by binding to histone proteins. The double stranded DNA forms a complex with histone proteins which is called a nucleosome. There are 8 histone proteins contained in one core of nucleosome.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 22
Correct
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Which of the following are true when it comes to tumour suppressor genes:
Your 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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 23
Correct
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The enzyme responsible for telomeres maintaining their length after cell division is called:
Your Answer: Telomerase
Explanation:Telomerase is the enzyme responsible for maintenance of the length of telomeres by addition of guanine-rich repetitive sequences. Telomerase activity is exhibited in gametes and stem and tumor cells.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 24
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 25
Correct
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Normal parents have a child with a recessive condition, Tay Sachs. The chance of them having a normal child is?
Your Answer: 75%
Explanation:The chance for normal parents having a child with a recessive disease is 1:4 or 25%. As both the parents are heterozygous for this condition. They have a 3:4 chance of having a normal child or 75%.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 26
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 27
Correct
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In which phase do chromosomes in the nucleus become 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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 28
Incorrect
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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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 29
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 30
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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