BIOL 1F90 Lecture Notes - Lecture 24: Gene Duplication, Hydrogen Bond, Psychological Stress

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Multiple rna primers are made: not made at origin, made near replication fork as single- stranded dna is available, direction is opposite to fork movement. Synthesis of dna is in pieces, okazaki fragments: fragments are eventually connected to each other to form a continuous lagging strand. As synthesis of both strands near completion: rna primers will be removed by a special. Dna polymerase and filled in with dna: dna ligase will join adjacent dna fragments. Dna helicase: binds to dna and travels 5(cid:495) to 3(cid:495) using atp to separate strand and move fork forward. Dna topoisomerase: relieves additional coiling ahead of replication fork. Single-strand binding proteins: keep parental strands open to act as templates. Covalently links nucleotides: deoxynuceloside triphosphates are used by the enzyme, adds nucleotides to 3(cid:495) end. Dna polymerase breaks a covalent bond to release pyrophosphate (2 phosphate groups: provides energy for polymerization, remaining deoxynucleoside monophosphate is covalently linked to the growing strand of dna.

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