1 / 15

DNA R eplication -II

DNA R eplication -II. Overview. I. General Features of Replication Semi-Conservative Starts at Origin Bidirectional Semi-Discontinuous II. Identifying Proteins and Enzymes of Replication III. Detailed Examination of the Mechanism of Replication Initiation Priming

gauri
Download Presentation

DNA R eplication -II

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. DNA Replication-II

  2. Overview I. General Features of Replication • Semi-Conservative • Starts at Origin • Bidirectional • Semi-Discontinuous II. Identifying Proteins and Enzymes of Replication III. Detailed Examination of the Mechanism of Replication • Initiation • Priming • Elongation • Proofreading and Termination

  3. Mechanism of DNA replication

  4. DNA replication system • Template: Double stranded DNA • Substrate:dNTP • Primer:Short RNA fragment with a free 3´-OH end • Enzyme:DNA-dependent DNA polymerase (DDDP),other enzymes, • protein factor.

  5. Overview of bacterial DNA replication

  6. DNA Polymerases Elongate DNA in the 5′→3′ Direction • First, all DNA polymerases require a template strandthat guides the polymerization reaction according to the Watson-Crick base-pairing rules. • Second, DNA polymerases require a primer strandthat is complementary to the template and contains a free 3′-OH group to which a nucleotide can be added. • Most primers are oligonucleotides of RNA rather than DNA, and specialized enzymes (primases) synthesize primers when and where they are required.

  7. DNA polymerases can only add nucleotides to a preexisting strand; they cannot synthesize DNA starting from only a template strand. Many different DNA polymerases have been studied from various types of bacteria, archaea, and eukaryotes, and mitochondria from many different species. All known DNA polymerases use the mechanism.

  8. The 3′-hydroxyl group of the primer strand, (dNMP)n, is activated to attack the α phosphorus of the incoming dNTP, resulting in attachment of a dNMP to the primer 3′ terminus and release of pyrophosphate (PPi). • The DNA polymerase active site must have at least two sites: • The template nucleotide that pairs with the incoming dNTP is positioned in the insertion site. • The primer 3′-terminal base pair is positioned in the postinsertion site.

  9. Most DNA Polymerases Contain DNA Exonuclease Activity DNA nucleases class of enzymes that degrade DNA Exonucleases Shorten DNA from the ends Endonucleases Cut DNA at internal positions Exonucleases degrades DNA in the 3′→5′ direction Exonucleases degrades DNA in the 5′→3′ direction Do you think the two DNA exonucleases of Pol I have the same active sites?

  10. The 3′→5′ Exonuclease: • When an incorrect dNMP is incorporated, the 3′→5′ exonuclease removes the mismatched nucleotide, giving the polymerase a second chance at incorporating the correct one. • This activity, known as proofreading, is not the reverse of the polymerization reaction- pyrophosphate is not involved, and the mismatched nucleotide is released as a dNMP, not a dNTP. • Also, proofreading by the 3′→5′ exonuclease occurs at a separate active site from polymerization. The 3′→5′ proofreading exonuclease of DNA polymerases.

  11. Most DNA polymerases contain this proofreading exonuclease activity, although some do not and thus become more capable of bypassing a DNA lesion.

  12. The 5′→3′ Exonuclease: • Pol I also contains a second exonuclease that degrades DNA in the 5′→3′ direction, the same direction as DNA synthesis. • The 5′→3′ exonuclease is unique to Pol I and reflects the enzyme’s role in DNA repair. • The 5′→3′ exonuclease is capable of functioning at the same time as the polymerase, because the two activities act in the same direction. Nick translation by Pol I. DNA polymerase I (Pol I) is organized into three major domains: DNA polymerase, 3′→5′ proofreading exonuclease, and 5′→3′ exonuclease. At a nick, the gap between lagging-strand fragments—Pol I degrades the RNA primer in the 5′→3′ direction, releasing NMPs, and simultaneously extends the 3′ terminus with dNTPs in the same direction. The net result is movement of the nick in the 5′→3′ direction along the DNA until all RNA is removed.

  13. Five E. coli DNA Polymerases Function in DNA Replication and Repair

  14. DNA polymerases require a primed template and extend the 3′ terminus of the primer strand by reaction with dNTPs. • A dNTP that correctly base-pairs to the template strand is incorporated into the primer strand with the release of pyrophosphate. Pyrophosphate is hydrolyzed by pyrophosphatase, which reduces the concentration of pyrophosphate in the cell and makes the reverse reaction extremely unlikely. • DNA polymerases are inherently very accurate, and are made even more accurate by a proofreading 3′→5′ exonuclease. • Pol I also contains a 5′→3′ exonuclease that degrades DNA while, at the same time, the polymerase synthesizes DNA, in the process of nick translation. • E. coli has five DNA polymerases. Pol III is responsible for chromosome replication, and Pol I is used to remove RNA primers and fill in the resulting gaps with DNA. The other three (II, IV, and V) are involved in DNA repair and in moving replication forks past sites of DNA damage.

More Related