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Question 1
Incorrect
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Which of the following is not true regarding mitochondrial chromosome disorders?
Your Answer: Most mitochondrial diseases are myopathies and neuropathies with a maternal pattern of inheritance
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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 2
Incorrect
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Immortality can result from over expression of which enzyme?
Your Answer: None of the above
Correct 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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Question 3
Incorrect
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Which part of the chromosome plays a role in preserving its integrity and stability?
Your Answer: Centromere
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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 4
Incorrect
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Telomerase is active in the following cells except:
Your Answer: Germ 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 5
Correct
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What is the structure of nucleosomes?
Your 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 6
Correct
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Regarding restriction fragment length polymorphisms (RFLP) and Gene Knockout Mouse Models. All are true except:
Your 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 7
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 8
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:Mitochondrial DNA (mtDNA) does indeed lack introns, meaning that its genes are closely packed with coding sequences. This actually means that any point mutation in the mtDNA is more likely to have an effect, not less. The lack of introns means there are fewer non-coding regions where mutations can occur without affecting gene function. Thus, mutations in mtDNA often have significant consequences because they are more likely to alter essential coding sequences.
The other statements are true:
- Most mitochondrial diseases are myopathies and neuropathies with a maternal pattern of inheritance: This is correct because mtDNA is inherited maternally, and many mitochondrial disorders affect muscle and nerve function.
- Retinal degeneration, diabetes mellitus, and some forms of hearing loss are some of the other diseases attributed to mitochondrial chromosome defects: These are indeed conditions associated with mitochondrial defects.
- Mitochondrial chromosome defects are inherited from one’s mother: This is correct, as mtDNA is passed from mother to offspring.
- Leber’s hereditary optic neuropathy (LHON), the commonest cause of blindness in young men, is an example of a mitochondrial chromosome defect: This is true; LHON is a well-known mitochondrial disorder.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 9
Correct
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Regarding Gene Knockout Mouse Models, all are true except:
Your 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).
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This question is part of the following fields:
- Genetics
- Medicine
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Question 10
Correct
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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.
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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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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.
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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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During which phase of the cell cycle does DNA synthesis occur?
Your 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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 13
Correct
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Which statement is incorrect regarding transcription of DNA?
Your 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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 14
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 15
Incorrect
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What is the role of cyclin and cyklin-dependent kinases in mitosis:
Your Answer: Causes splitting of the centromere
Correct 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 16
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 17
Incorrect
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Defects in chromosomal structure (and examples) include those mentioned below except:
Your Answer: Deletion (Wilms’ tumour, deletions of part of p11)
Correct 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.
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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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With regard to X linked disorders which of the following are true
Your Answer: None of the above
Correct 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.
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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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Question 20
Incorrect
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Question 21
Incorrect
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During which phase of meiosis does exchange of genetic material occur accounting for genetic diversity between individuals:
Your Answer: Interphase
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.
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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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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 23
Incorrect
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Which of the following statements is not true about mitochondrial chromosomes?
Your Answer: Encode proteins that are critical to the process of apoptosis
Correct 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 24
Incorrect
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 25
Incorrect
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“Ploidy” is a term used to refer to the number of chromosomes in cells. Cancer cells are commonly:
Your Answer: Tetraploidy
Correct Answer: Aneuploidy
Explanation:Cancer cells most commonly undergo disordered cell growth and cell division. This results in an additional number of chromosomes called aneuploidy. This is a characteristic of cancer cells along with variation in differentiation of the cells.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 26
Incorrect
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In a knockout mouse model the process used to combine the new DNA sequence and the stem cells is known as:
Your Answer: Recombination
Correct Answer: Insertion
Explanation:Chimerisation is also known as the formation of recombinant DNA. When a foreign DNA sequence is inserted into a plasmid or other DNA sequence, this process is known as insertion.
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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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Question 28
Incorrect
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When during the cell cycle do the centrioles replicate?
Your Answer: S phase
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.
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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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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 30
Incorrect
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Which of the following with regard to DNA mutations does not fit:
Your Answer: All of them fit
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.
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This question is part of the following fields:
- Genetics
- Medicine
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