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Chapter 16 The Molecular Basis of Inheritance Teaching Objectives DNA Replication and Repair 1. Describe the process of DNA replication, including the role of the origins of replication and replication forks. 2. Explain the role of DNA polymerases in replication. 3. Explain what energy source drives the polymerization of DNA. 4. Define antiparallel and explain why continuous synthesis of both DNA strands is not possible. 5. Distinguish between the leading strand and the lagging strand. 6. Explain how the lagging strand is synthesized even though DNA polymerase can add nucleotides only to the 3’ end. Describe the significance of Okazaki fragments. 7. Explain the roles of DNA ligase, primer, primase, helicase, topoisomerase, and singlestrand binding proteins. 8. Explain the roles of DNA polymerase, mismatch repair enzymes, and nuclease in DNA proofreading and repair. 9. Describe the structure and function of telomeres. 10. Explain the possible significance of telomerase in germ cells and cancerous cells. *Key to remember: DNA Polymerase READS DNA in the 3’ 5’ direction, but BUILDS in the 5’ 3’ direction Key Terms DNA ligase double helix lagging strand mismatch repair nucleotide excision repair origin of replication primase replication fork single-strand binding protein telomere transformation DNA polymerase helicase leading strand nuclease Okazaki fragment phage primer semiconservative model telomerase topoisomerase Chapter 17 The Connection Between Genes and Proteins 1. 2. 3. 4. 5. From Gene to Protein * = Not covered in class Explain how RNA differs from DNA. Briefly explain the Central Dogma. Distinguish between transcription and translation. Compare where transcription and translation occur in prokaryotes and in eukaryotes. Define codon and explain the relationship between the linear sequence of codons on mRNA and the linear sequence of amino acids in a polypeptide. 6. Explain why polypeptides begin with methionine when they are synthesized. 7. Explain what it means to say that the genetic code is redundant and unambiguous. * 8. Explain the significance of the reading frame during translation. The Synthesis and Processing of RNA 9. Explain how RNA polymerase recognizes where transcription should begin. Describe the promoter, the terminator, and the transcription unit. 10. Explain the general process of transcription, including the three major steps of initiation, elongation, and termination. 11. Explain how RNA is modified after transcription in eukaryotic cells. 12. Describe the functional and evolutionary significance of introns. The Synthesis of Protein 13. Describe the structure and functions of tRNA. 14. Explain the significance of wobble. * 15. Describe the process of translation (including initiation, elongation, and termination) and explain which enzymes, protein factors, and energy sources are needed for each stage. 16. Describe the significance of polyribosomes. * 17. Explain what determines the primary structure of a protein and describe how a polypeptide must be modified before it becomes fully functional. * 18. Describe what determines whether a ribosome will be free in the cytosol or attached to the rough endoplasmic reticulum. * 19. Compare protein synthesis in prokaryotes and in eukaryotes. 20. Define point mutations. Distinguish between base-pair substitutions and base-pair insertions. Give examples of each and note the significance of such changes. 21. Describe several examples of mutagens and explain how they cause mutations. Key Terms 5’ cap base-pair substitution exon intron mutagen point mutation primary transcript ribosomal RNA (rRNA) RNA processing signal-recognition particle (SRP) template strand transcription factor transfer RNA (tRNA) wobble alternative RNA splicing codon frameshift mutation messenger RNA (mRNA) mutation poly-A tail promoter ribosome RNA splicing spliceosome terminator transcription initiation complex translation anticodon deletion insertion missense mutation nonsense mutation polyribosome (polysome) reading frame RNA polymerase signal peptide TATA box transcription transcription unit triplet code Chapter 18 1. Explain the adaptive advantage of genes grouped into an operon. 2. Using the trp operon as an example, explain the concept of an operon and the function of the operator, repressor, and corepressor. 3. Distinguish between structural and regulatory genes. 4. Describe how the lac operon functions and explain the role of the inducer, allolactose. 5. Explain how repressible and inducible enzymes differ and how those differences reflect differences in the pathways they control. 6. Distinguish between positive and negative control and give examples of each from the lac operon. 7. Explain how cyclic AMP and catabolite activator protein are affected by glucose concentration. 8. Which operons are used for catabolic vs. anabolic process?