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IB Biology (HL)
Genetics and evolution
dna replication
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IB Biology (HL)
Genetics and evolution
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DNA Replication
The process of producing exact copies of DNA with identical base sequences, essential for reproduction, growth, and tissue replacement.
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Semi-Conservative Replication
A method of DNA replication where each new DNA molecule consists of one original strand and one newly synthesized strand.
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Helicase
An enzyme that unwinds DNA by breaking the hydrogen bonds between complementary base pairs during replication.
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DNA Polymerase
An enzyme that adds nucleotides to the growing DNA strand during replication, following the rules of complementary base pairing.
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DNA Primase
An enzyme that synthesizes RNA primers to provide starting points for DNA polymerase in replication.
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Okazaki Fragments
Short fragments of DNA synthesized on the lagging strand during DNA replication, requiring multiple RNA primers.
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Polymerase Chain Reaction (PCR)
A technique used to amplify small segments of DNA, enabling analysis and research.
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Gel Electrophoresis
A method for separating DNA fragments based on size by applying an electric current to a gel containing the DNA.
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Short Tandem Repeats (STRs)
Repeated DNA sequences between 1-6 base pairs in length, used in forensic DNA profiling and paternity tests due to their variability.
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Directionality of DNA Polymerases
DNA polymerases add nucleotides in a 5' to 3' direction, which is crucial for the process of DNA replication.
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DNA Proofreading
The mechanism by which DNA polymerase III checks and corrects mismatched nucleotides after they are added to the growing DNA strand.
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DNA Ligase
An enzyme that seals gaps between Okazaki fragments on the lagging strand to create a continuous DNA molecule.
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Complementary Base Pairing
The specific pairing of nucleotide bases where adenine pairs with thymine and cytosine pairs with guanine, ensuring accurate replication.
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Taq Polymerase
A thermophilic DNA polymerase commonly used in PCR due to its ability to withstand high temperatures.
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Denaturation (PCR)
The first step in PCR; involves heating the DNA sample to separate the strands.
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Annealing (PCR)
The second step in PCR; cooling the sample to allow RNA primers to attach to the single-stranded DNA.
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Synthesis (PCR)
The third step of PCR; where Taq polymerase adds nucleotides to extend the new DNA strands.
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