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Question 1
Incorrect
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Defects in chromosomal structure (and examples) include those mentioned below except:
Your Answer: Duplication (Charcot-Marie-tooth syndrome; duplication of a region of chromosome 17)
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 2
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 3
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: Krebs cycle
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 4
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 5
Incorrect
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The enzyme responsible for Telomeres to maintain their length after cell division is called:
Your Answer: None of the above telomeres shorten with all cell divisions
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 6
Incorrect
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Which of the following statements is not true about mitochondrial chromosomes?
Your Answer: Are circular DNA molecules of approximately 16 500 base pairs, and every base-pair makes up part of the coding sequence
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 7
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 8
Incorrect
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Regarding Southern Blotting and DNA probes, which answer is FALSE
Your Answer: Gene probes can be labelled with radioactive isotopes g 32 p
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 9
Incorrect
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Which statement about X linked dominant disorders is FALSE?
Your Answer: Half of the male or female offspring of an affected mother will have the disease.
Correct 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 10
Correct
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Question 11
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: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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 12
Incorrect
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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
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Question 13
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 14
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 15
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 16
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 17
Correct
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Question 18
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 19
Correct
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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.
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This question is part of the following fields:
- Genetics
- Medicine
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Question 20
Incorrect
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Which statement is correct?
Your Answer: Mitochondrial DNA has a double helix structure and also has a critical role in apoptosis.
Correct 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.
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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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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 22
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 23
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 24
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 25
Incorrect
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Southern Blotting and DNA probes:
Your Answer: Gene probes can consist of DNA or RNA
Correct 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.
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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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The process where by DNA fragments are separated by size and charge is called:
Your Answer: PCR
Correct 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 27
Correct
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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.
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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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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 29
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 30
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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SESSION STATS - PERFORMANCE PER SPECIALTY
