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7.1 DNA Replication Mechanisms

3 min readaugust 9, 2024

DNA replication is a crucial process for cell division and genetic inheritance. It involves a complex machinery of enzymes and proteins working together to accurately duplicate the genome. This topic explores the key players and mechanisms involved in DNA replication.

The replication process follows a semiconservative model, with leading and occurring simultaneously at the . Understanding these mechanisms is essential for grasping how cells maintain genetic integrity across generations.

DNA Replication Enzymes

Essential Enzymes in DNA Replication

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  • catalyzes the addition of nucleotides to the growing DNA strand
    • Adds nucleotides in the 5' to 3' direction
    • Possesses capability to ensure accuracy
    • Multiple types exist (I, II, III) with distinct functions
  • unwinds the DNA double helix
    • Breaks hydrogen bonds between base pairs
    • Creates single-stranded DNA templates for replication
    • Moves along the DNA in the 5' to 3' direction
  • synthesizes short RNA primers
    • Generates RNA primers complementary to the DNA template
    • Provides a starting point for DNA polymerase
    • Typically creates primers 8-12 nucleotides long

Supporting Enzymes and Specialized Replication Proteins

  • joins on the lagging strand
    • Seals gaps between adjacent DNA segments
    • Forms phosphodiester bonds between nucleotides
    • Requires energy in the form of ATP
  • maintains the ends of linear chromosomes
    • Adds repetitive DNA sequences to chromosome ends
    • Prevents loss of genetic material during replication
    • Contains both protein and RNA components
  • stabilize single-stranded DNA
    • Prevent reformation of double-stranded DNA
    • Protect exposed DNA from nuclease degradation
  • relieves tension in the DNA ahead of the replication fork
    • Introduces temporary breaks in the DNA backbone
    • Allows for unwinding of supercoiled DNA

Replication Process

Fundamental Mechanisms of DNA Replication

  • ensures accurate DNA duplication
    • Each new double helix contains one original strand and one new strand
    • Maintains genetic information across cell divisions
    • Demonstrated by Meselson and Stahl experiment (1958)
  • occurs continuously
    • DNA polymerase moves in the same direction as the replication fork
    • Requires only one RNA primer at the
    • Synthesized in the 5' to 3' direction
  • Lagging strand synthesis occurs discontinuously
    • DNA polymerase moves in the opposite direction of the replication fork
    • Requires multiple RNA primers
    • Synthesized in short segments called Okazaki fragments

Structural Components and Processes at the Replication Fork

  • Okazaki fragments form during lagging strand synthesis
    • Short DNA segments approximately 100-200 nucleotides long
    • Named after discoverers Reiji and Tsuneko Okazaki
    • Joined by DNA ligase to form a continuous strand
  • Replication fork serves as the site of active DNA synthesis
    • Y-shaped structure where parental DNA strands separate
    • Contains both leading and lagging strand templates
    • Moves along the DNA as replication progresses
  • form when multiple origins initiate replication
    • Allow for bidirectional replication in eukaryotes
    • Merge as replication proceeds along the chromosome
    • Increase the overall speed of DNA replication

Replication Initiation

Origin of Replication and Initiation Complexes

  • Origin of replication marks the starting point for DNA synthesis
    • Specific DNA sequences recognized by
    • Varies in number between prokaryotes and eukaryotes
    • Prokaryotes typically have a single origin (OriC in E. coli)
    • Eukaryotes possess multiple origins along each chromosome
  • Initiator proteins bind to the origin to start replication
    • in prokaryotes
    • (ORC) in eukaryotes
    • Recruit additional proteins to form the

Regulation and Timing of Replication Initiation

  • Cell cycle control regulates the timing of replication initiation
    • Ensures DNA is replicated only once per cell cycle
    • Involves (CDKs) in eukaryotes
    • Prevents re-replication through licensing factors
  • varies across the genome
    • Early and late-replicating regions exist in eukaryotes
    • Correlates with chromatin structure and gene activity
    • Helps coordinate replication with transcription and cell division
  • affects replication initiation
    • Not all potential origins fire in every cell cycle
    • Flexible usage allows for adaptation to cellular conditions
    • Dormant origins can be activated under replication stress
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© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.

© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.
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