Lecture 7: Replication Flashcards
deoxyribonucleotide triphosphate (dNTP)
- nucleotide
How do prokaryotes replicate their DNA?
- DNA polymerase unzips helix
- 5’–>3’ in both directions
- replication forks and bubbles (see notes)
synthesis of leading strand (2 steps) (4 key enzymes/proteins involved in first step, SHPT; 1 involved in second)
- DNA is opened and primed:
- primase makes RNA primer (~10 nucleotides long)
- topoisomerase removes twists
- helicase opens double helix
- single strand DNA binding proteins keeps strands separated - DNA polymerase III makes leading strand 5’–>3’
synthesis of lagging strand (5 steps)
- RNA primer is added
- first fragment synthesized
- next fragment is synthesized (okazaki fragments)
- replace primer (DNA primer I replaces RNA with DNA and goes 5’–>3’)
- gap is closed by DNA ligase
How does DNA replication occur in Eukaryotes? What is the problem that eukaryote cells run into at the end of replication?
- similar to prokaryotes except larger and more linear chromosomes with multiple replication forks
- at the end of replication a problem occurs where there are missing nucleotides at the 5’ end because chromosomes shorten during replication
telomer and telomerase
- telomer: portion of strand (end piece) missing DNA (the unreplicated 5’ end)
- telomerase binds to a 3’ end and adds nucleotides to lengthen telomer several times; has its own RNA template
- extended DNA acts as a template for DNA polymerase III
DNA repair:
- during replication
- immediately after replication
- anytime
- during: DNA polymerase proofreads DNA; wrong nucleotides are excised and replaced
- immediately after replication: mismatched repair occurs on new strand
- anytime: repair of damaged DNA
enzymes involved in DNA repair (3): state role
- nucleases: excision
- DNA polymerase: replacement
- ligase: linkage
genotype vs phenotype
genotype: sequence code for protein
phenotype: physical trait produced by protein
List the types of mutations (4)
- silent
- missense
- nonsense
- frameshift
explain the following mutation type and the result of it: silent
- change in nucleotide sequence that does not impact the amino acid specified by codon
- result: no change in phenotype
explain the following mutation type and the result of it: missense
- change in nucleotide sequence that changes amino acid specified by codon
- result: change in primary structure of protein (could be beneficial, neutral, or deleterious)
explain the following mutation type and the result of it: nonsense
- change in nucleotide sequence that results in an early stop codon
- result: breakdown of mRNA or a shortened polypeptide; usually deleterious
explain the following mutation type and the result of it: frameshift
- addition/ deletion of a nucleotide
- result: reading frame is shifted altering meaning of all subsequent codons; almost always deleterious
differentiate between DNA I and DNA III
- dna polymerase I: removes RNA primer with DNA
- dna polymerase iii: adds nucleotides to make new strand