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To study the processing of pre-mRNA transcripts, the researcher cultured human myocytes in the laboratory and used a technique called ultracentrifugation to isolate myocyte nuclei, ribosomes and cytoplasm.
Which isolated sample (nuclei, ribosomes or cytoplasm) would contain the greatest abundance of pre-mRNA transcripts? Briefly justify your response. (1-2 sentences) (2 marks)
i) Which type of alternative splicing event generated mRNA Transcript B? Provide a brief justification for your response. (1-2 sentences) (1 mark)
ii) Which type of alternative splicing event generated mRNA Transcript C? Provide a brief justification for your response. (1-2 sentences) (1 mark)
To determine which aspect of carbon catabolism was impacted by mutagenesis in each of these strains, the strains were also assayed for carbon catabolism of glucose, xylose and arabinose and sent for genetic sequencing. It was found that PET #X had a mutation that resulted in constitutive CAP binding to the CAP binding site. Which of the graphs below is most likely to represent strain PET #X?
The randomly generated mutants were then screened for ethanol production. Strains were cultured in media containing glucose, xylose and arabinose to reflect the composition of agricultural biomass. The bacterial strains were cultured for a period of fifteen hours and samples of media were collected at regular timepoints (0, 3, 6, 9, 12 and 15 hours) to track the production of ethanol.
A graph of ethanol production in the PET #A strain and 2 mutant strains; PET #X, and PET #Y are shown below.
Which strain produced the most ethanol at 15 hours?
The researcher treated PET #A E. coli with the base analogue 2-Aminopurine which is structurally similar to a nitrogenous base found in DNA. The structure of 2-Aminopurine is shown below:
Which nitrogenous base does 2-Aminopurine
most closely resemble?
The ecologists used a quantitative PCR (qPCR) assay to investigate the abundance of the novel organism in several different ecological niches including hydrothermal vents, deep-sea sediments and shallow coastal waters. The qPCR assay was performed using a primer that specifically targeted a gene carried by the novel organism.
Examine the qPCR results shown above. Which ecological niche (hydrothermal vents, deep-sea sediments, shallow coastal waters) had the highest abundance of the novel organism? Briefly explain how you reached this conclusion. (2-3 sentences) (2 marks)
The ACTC1 gene encodes an actin protein that is only expressed in cardiomyocytes (i.e. cardiac muscle cells). The schematic below shows the histone modifications that are present in the promoter region in cardiomyocytes vs fibroblasts (i.e. skin cells).
Use the information provided above to explain why the gene is actively expressed in cardiomyocytes but not fibroblasts. (2-3 sentences) (2 marks)
The ACTB gene encodes an actin protein that is ubiquitously expressed in all human cells. As shown in the schematic below, the promoter region of the gene is embedded within a CG island.
The researcher uses a specialised laboratory technique to examine DNA methylation in the promoter region. What do you hypothesise the researcher will find? (1 mark)
Q5. Concisely describe the patient’s sequence variant in a format suitable for the results section of a scientific report. Your answer must include the gene name, reference sequence accession number, correct DNA-level and protein-level notation, and appropriate gene and protein nomenclature.
A sequence variant was identified in exon 14 of the patient's
Q3. How would you classify the patient's sequence variant at the DNA level?