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Question 1
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 2
Correct
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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: 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 3
Correct
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Which of the following conditions is NOT X-linked recessive?
Your Answer: Cystic fibrosis
Explanation:Cystic fibrosis is a autosomal recessive disease with an incidence of about 1 in 2500 live births. The most common mutation occurs in the long arm of chromosome 7 which codes for the chloride channel (cystic fibrosis transmembrane conductance regulator) gene.
To have CF, a child must inherit two abnormal genes—one from each parent. The recessive CF gene can occur in both boys and girls because it is located on non-sex-linked chromosomes called autosomal chromosomes.
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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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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.
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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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Question 6
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 7
Correct
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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: 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 8
Correct
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Restriction Enzymes...
Your Answer: Cut DNA sequences at specific sites
Explanation:Restriction endonucleases are enzymes that recognise short sequences of double stranded DNA and cut them at specific nucleotide points or sequences. These sequences differ for different restriction endonucleases.
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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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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 10
Correct
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Which of the following is false with regard to the following statement: Proto- oncogenes can be transformed to oncogenes in the following ways.
Your Answer: Inhibition of P53
Explanation:Proto oncogenes cannot be transformed into oncogenes due to inhibition of P53 gene. There has to be a mutation in the proto oncogene. All the other options are true.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 11
Correct
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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.
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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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The telomerase is capable of adding several more repeats of telomeres at which end of the guanosine rich region.
Your 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 13
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 14
Correct
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“Ploidy” is a term used to refer to the number of chromosomes in cells. Cancer cells are commonly:
Your 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 15
Correct
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Question 16
Correct
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Consanguinity shows a strong association with which pattern of inheritance?
Your 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
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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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Question 18
Correct
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The following cells replicate without shortening their telomeres because they express telomerase.
Your Answer: Germ cells
Explanation:Telomerase activity is seen in germ cells and is absent in somatic cells. Telomeres prevent the chromosomes from shortening and prevent the coding portion of the DNA from being lost, thus allowing the cell to replicate indefinitely. During replication telomeres may be lost resulting in cell death.
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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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When 2 nucleotide chains of DNA bind together, thymine is bound to:
Your Answer: Adenine
Explanation:As a general rule in the structure of DNA, thymine always binds to adenine with two hydrogen bonds, cytosine always binds to guanine with three hydrogen bonds and vice versa. However In the structure of RNA the only difference is that adenine binds to uracil instead of thymine. But thymine will always bind to adenine.
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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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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 21
Correct
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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.
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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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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 23
Correct
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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.
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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 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.
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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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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.
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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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When during the cell cycle do the centrioles replicate?
Your 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 27
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 28
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 29
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 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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Question 31
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 25% chance of inheriting the chromosome carrying the disease allele
Correct Answer: The offspring of a heterozygous individual has a 50% chance of inheriting the chromosome carrying the disease allele
Explanation:50% of the children will be effected from parents who are heterozygous for an autosomal dominant disorder. An allele can be dominant or recessive. Individuals, meanwhile, can be homozygous or heterozygous: individuals who are homozygous for a certain gene carry two copies of the same allele. individuals who are heterozygous for a certain gene carry two different alleles.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 32
Incorrect
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In which phase do chromosomes in the nucleus become completely 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
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This question is part of the following fields:
- Genetics
- Medicine
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Question 33
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 34
Incorrect
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 35
Incorrect
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The mitochondrial chromosome is a circular DNA molecule. They encode for proteins needed for ATP production. These proteins are also essential for:
Your Answer: Cellular aging
Correct Answer: Apoptotic cell death
Explanation:The intrinsic pathway or the mitochondrial pathway of apoptosis is activated due to the loss of BCL-2 and other antiapoptotic proteins. This loss results in the increased membrane permeability and release of cytochrome C which activates caspases downstream resulting in apoptosis.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 36
Incorrect
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Which of the following is not true regarding mitochondrial chromosome disorders?
Your Answer: Retinal degeneration, diabetes mellitus and some forms of hearing loss are some of the other disease attributed to mitochondrial chromosome defects
Correct 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 37
Incorrect
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What is the role of cyclin and cyklin-dependent kinases in mitosis:
Your Answer:
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 38
Incorrect
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Regarding Southern Blotting and DNA probes, which answer is FALSE
Your Answer:
Correct 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 39
Incorrect
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Question 40
Incorrect
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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:
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.
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This question is part of the following fields:
- Genetics
- Medicine
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SESSION STATS - PERFORMANCE PER SPECIALTY
