Nucleic Acids and Protein Synthesis
137 questions· page 1 of 14
In step 2 in Fig. 3.1, the single-stranded primary transcript loops and forms a section where dsRNA is present.
Explain how it is possible for the double-stranded section of RNA to be held together in step 2 and maintained this way in steps 3, 4 and 5.
After step 3, the shorter dsRNA produced by the action of Drosha is transported to the cytoplasm, where it is cleaved further by Dicer to produce ds siRNA.
Suggest why two different enzymes, Drosha and Dicer, are needed to cut dsRNA into shorter lengths.
From 2018, siRNA has been used as a therapeutic drug to treat a number of diseases.
The presence of molecules of siRNA in the cytoplasm can result in the cleavage of messenger RNA (mRNA) molecules coding for a protein involved in the disease. This prevents the synthesis of the protein.
Describe the differences between a molecule of mRNA and a molecule of siRNA, such as the siRNA shown in step 5 in Fig. 3.1.
With reference to Fig. 3.2, state why the passenger strand needs to be separated and released from the RISC.
The aim of siRNA therapy is to prevent or decrease the synthesis of a protein involved in the disease being treated.
A target mRNA molecule can be cleaved in a different location by a RISC with a different siRNA.
Suggest how cleaving mRNA in different locations will have different effects on protein synthesis and explain how these different effects can result in a lack of functioning protein.
Describe three ways in which the structure of messenger RNA (mRNA) differs from the structure of DNA.
In each of your answers, include information about the structure of mRNA and the structure of DNA.
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2
3
State and explain which DNA base pair is most similar to the synthetic base pairs in Fig. 6.1.
Identify and describe the DNA-RNA nucleotide pair shown in Fig. 3.1.
You may add labels and annotations to Fig. 3.1 if you wish.
Fig. 3.2 shows a stage in the replication of DNA. The circled part is enlarged in Fig. 3.3 to show the elongation of the DNA strand that is being synthesised.
Describe the sequence of events that occurs at the stage shown in Fig. 3.3 to extend the synthesised strand.
The two strands in a molecule of DNA are described as antiparallel.
With reference to Fig. 3.2 and Fig. 3.3, state what is meant by antiparallel, and explain how the antiparallel arrangement of the strands determines how new strands are synthesised.
The names of the bases present in RNA and DNA nucleotides can be abbreviated using a single letter. These are shown in Table 5.1.
Complete Table. 5.1 by stating:
- the name of each base
- whether the base is a purine or pyrimidine
- whether the base is present
- only in an RNA molecule (write RNA in the table)
- only in a DNA molecule (write DNA in the table)
- in RNA and in DNA molecules (write the word both in the table).
Table 5.1
| base | name of base | purine or pyrimidine | present in RNA, DNA, or both |
|---|---|---|---|
| A | |||
| C | |||
| G | |||
| T | |||
| U |
With reference to Fig. 5.1, explain whether carbovir triphosphate will replace a purine or a pyrimidine nucleotide in the elongating polynucleotide chain.
With reference to Fig. 5.1 and the action of DNA polymerase, suggest why the conversion of abacavir to carbovir triphosphate increases the chance of the analogue being added to the viral polynucleotide chain.
Suggest and explain how carbovir triphosphate interferes with the action of DNA polymerase and how this may prevent the synthesis of viral DNA.
Fig. 6.2 shows the RNA base sequence of a short length of primary transcript.
Complete Fig. 6.2 by writing the DNA base sequence of the template strand used to form the primary transcript.
In eukaryotic cells, the primary transcript is modified to form mRNA.
Explain how the primary transcript is modified to form mRNA.
The mRNA strand is translated at the ribosome to form a polypeptide.
Describe how the process of translation results in the formation of a polypeptide.
Mutagenesis is a process that leads to a change in the amino acid sequences of proteins. Scientists carry out mutagenesis to investigate the importance of particular amino acids in protein structure and function.
Outline how changing one amino acid in the -globin polypeptide of haemoglobin may change the structure and function of a molecule of haemoglobin.