Chemical Basis of Bioengineering I

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Okazaki Fragments

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Chemical Basis of Bioengineering I

Definition

Okazaki fragments are short sequences of DNA that are synthesized on the lagging strand during DNA replication. These fragments are essential for the overall process of DNA synthesis, as they allow for the replication of the DNA template in a discontinuous manner, leading to the eventual formation of a continuous strand through the action of DNA ligase.

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5 Must Know Facts For Your Next Test

  1. Okazaki fragments typically range from 100 to 200 nucleotides in length in eukaryotic cells and about 1,000 to 2,000 nucleotides in prokaryotic cells.
  2. These fragments are produced because DNA polymerase can only synthesize DNA in the 5' to 3' direction, leading to discontinuous synthesis on the lagging strand.
  3. Each Okazaki fragment begins with an RNA primer, which is synthesized by primase, providing a starting point for DNA polymerase.
  4. After synthesis, RNA primers are removed and replaced with DNA nucleotides before being joined together by DNA ligase to complete the lagging strand.
  5. The discovery of Okazaki fragments was made by Japanese scientist Reiji Okazaki in the 1960s and helped clarify the mechanism of DNA replication.

Review Questions

  • How do Okazaki fragments contribute to the overall process of DNA replication?
    • Okazaki fragments allow for the synthesis of the lagging strand during DNA replication. Since DNA polymerase can only add nucleotides in the 5' to 3' direction, these short segments are synthesized discontinuously as the replication fork opens up. After their formation, these fragments are later connected by DNA ligase, which creates a continuous strand and ensures that both strands of the DNA molecule are accurately replicated.
  • Discuss the role of enzymes involved in the synthesis and joining of Okazaki fragments during DNA replication.
    • During DNA replication, several key enzymes work together to synthesize and join Okazaki fragments. Primase lays down RNA primers that provide starting points for DNA polymerase to begin synthesis of each fragment. Once synthesized, these fragments have RNA primers that need removal; this task is handled by another enzyme called RNase H. Finally, DNA ligase seals the gaps between Okazaki fragments, forming a continuous strand on the lagging side of the replication process.
  • Evaluate how disruptions in Okazaki fragment processing could affect cellular functions and genomic integrity.
    • Disruptions in the processing of Okazaki fragments can lead to incomplete or erroneous DNA replication, which can compromise genomic integrity. If DNA ligase fails to properly join these fragments, it could result in gaps or mutations within the lagging strand. Such defects may cause genomic instability, contributing to diseases like cancer or affecting normal cell functions such as growth and division. Understanding these processes underscores the importance of accurate replication mechanisms for maintaining healthy cells.
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