Concept explainers
To answer:
Prevention of protein synthesis by mutated gene through recombinant DNA technology.
Introduction:
In translation, mRNA is converted into amino acid sequences, resulting in protein synthesis. Three important components are involved in translation are m-RNA, t-RNA, and the ribosome. Protein synthesis occurs in the cytoplasm of the cell. The mRNA sequence encoded by the genetic material is translated into a specific protein. The t-RNA binds to free amino acids and transfer them to the ribosome and the amino acids are added to the growing chain of the protein sequence. The ribosome reads mRNA and synthesizes protein based on codons present in the mRNA sequence. The ribosome binds to the anticodon of particular t-RNA according to m-RNA sequence and assembles amino acids corresponding to m-RNA codons. Three
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EP MICROBIOLOGY:W/DISEASES BY..-MOD.ACC
- Construct a table, concept map, or picture to summarize how base analogues, DNA-modifying agents, and intercalating agents cause mutationsarrow_forwardBriefly explain about computer-automated high-throughput DNA sequencing ?arrow_forwardHow can site-specific recombination be used in recombinant DNA technology? Explain with an examplearrow_forward
- b) Describe how DNA is digested by different restriction enzymes c) Describe how gel electrophoresis is used to estimate the size of DNA fragments.arrow_forwardA patient is diagnosed with lung cancer using imaging. To establish the best treatment option, doctors ask to profile the gene expression of the tumor, using a biopsy and microarray analysis. Describe the steps involved in the analysis in detail. The analysis reveals that a new gene therapy could be beneficial to the patient. Explain briefly how gene therapy could be used to cure cancer and detail how the treatment can be formulated for delivery to the patient. To prepare DNA for the gene therapy formulation, it is often important to measure the size of the molecule. Explain how this measurement can be done using agarose gel electrophoresis, taking care to detail the property of the DNA molecule at the basis of the technique. To generate large amounts of DNA to manufacture gene therapy payloads or to be able to see them on gel electrophoresis, specific sequences can be amplified by PCR. For a sequence of a 100 base pairs, calculate the number cycles of PCR required to generate 1 ng of…arrow_forwardExplain why exome sequencing can be almost as valuable as genome sequencing.arrow_forward
- Briefly present experimental and practical benefits of using PCR in DNA cloning process. Give some examples of clinical applications.arrow_forwardDescribe the important features of cloning vectors. Explain the purpose of selectable markers in cloning experiments.arrow_forwardAs shown , several medical agents are now commercially produced by genetically engineered microorganisms. Discuss the advantages and disadvantages of making these agents this way.arrow_forward
- What specifically will happen if DNA polymerase is inaccurate during DNA synthesis? Explain how this inaccuracy might affect the organism.arrow_forwardJackson Wang is a biologist working with the genetics of a thermophilic bacterium. He cloned a heat shock gene from the bacteria for further analysis. After cloning, he isolated the plasmid carrying his gene of interest for sequencing. Jackson finally received the nucleotide sequence of his gene. Explain in detail how he could verify whether the nucleotide sequence matches his gene of interest using the bioinformatics databases available.arrow_forwarda) What are vectors? Describe extensively the roles vectors play in genetic engineering? Write short notees on the following: Recombinant DNA, Cloning b) What are restriction enzymes? Describe extensively the roles restriction enzymes play in genetic engineering? Write short notees on the following: Selectable markers, Cloningarrow_forward
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