DNA Replication.

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Presentation transcript:

DNA Replication

Cell Division occurs after DNA has replicated Cell Division occurs after DNA has replicated. - occurs in the S phase of Interphase Occurs so that each daughter cell can have its own copy of the instruction book (DNA) Occurs in the nucleus

Requires new nucleotides and replication enzymes. Gyrase (Topoisomerase) Helicase Single Strand Binding Proteins RNA Primase DNA Polymerase Ligase

Process of Replication 1. Gyrase unspools the DNA. DNA is wound around itself in the nucleus. Gyrase straightens it out for helicase to work. Many drugs operate through interference with the topoisomerases. The broad-spectrum fluoroquinolone antibiotics act by disrupting the function of bacterial type II topoisomerases. These small molecule inhibitors act as efficient anti-bacterial agents by hijacking the natural ability of topoisomerase to create breaks in chromosomal DNA. Some chemotherapy drugs called topoisomerase inhibitors work by interfering with mammalian-type eukaryotic topoisomerases in cancer cells. This induces breaks in the DNA that ultimately lead to programmed cell death (apoptosis). This DNA-damaging effect, outside of its potential curative properties, may lead to secondary neoplasms in the patient.

2. Helicase binds to the start point of replication and separates the two strands of DNA by breaking the adenine from the thymine and the guanine from the cytosine.

3. Single Strand Binding Proteins attach to each side of the DNA to keep the strands separated.

4. RNA Primase builds a small section of RNA across from the DNA 4. RNA Primase builds a small section of RNA across from the DNA. This is called an RNA primer and acts as the starting point for DNA to start building. This is like the foundation of a house. You don’t just build the house on the ground, you need something flat and solid to build on.

5. DNA Polymerase adds new nucleotides to the end of the 3’ end of the RNA primer building from in the 5’ to 3’ direction. It can only add new nucleotides to the 3’ end of another nucleotide. Builds unidirectionally. The nucleotides build continuously on this side of the RNA primer and is called the leading strand.

DNA ANIMATION

New DNA is built complementary to the old strand New DNA is built complementary to the old strand. DNA polymerase matches the DNA nucleotides to the opposite pair. A’s are matched with new T’s, G’s are matched with new C’s, etc. Parent (original) Strand of DNA: AGTCGATAGC Complementary Daughter (new) Strand:

New DNA is built complementary to the old strand New DNA is built complementary to the old strand. DNA polymerase matches the DNA nucleotides to the opposite pair. A’s are matched with new T’s, G’s are matched with new C’s, etc. Parent (original) Strand of DNA: AGTCGATAGC Complementary Daughter (new) Strand: TCAGCTATCG

Because DNA can only be built unidirectionally (on the 3’ of the previous nucleotide), new nucleotides cannot be added to the other side of the 5’ end. Therefore another RNA primer must be added to the DNA “downstream” from the first RNA primer. The DNA polymerase then adds nucleotides to the 3’ end and builds the DNA in a short segment. As the helicase continues to unwind the DNA, new primers are added building numerous short strands, called Okazaki fragments. This side of the DNA, since it is built in short segments, takes longer to build than the other side. Therefore it is called the lagging strand. DNA ANIMATION DNA ANIMATION II

6. Once the DNA has been built, another form of DNA polymerase removes the RNA primers and replaces them with DNA. 7. DNA Ligase binds the Okazaki fragments together. DNA ANIMATION

Both sides of the DNA strands are replicated at the same time Both sides of the DNA strands are replicated at the same time. Since they are anti-parallel (run opposite directions), the leading and lagging strands of each side are opposite of one another. Each original strand (parent strand) acts as the template for the new strand (daughter strand). Since each of the copies of DNA contains one half parent (original) DNA and one half daughter (new) DNA, DNA replication is said to be SEMI-Conservative. DNA ANIMATION A more realistic representation

Problems with Replication 1. Replication Errors: sometimes the wrong nucleotide is put in place (one in a billion) . A third type of DNA polymerase scans the newly replicated DNA for errors and cuts them out and corrects them  DNA spellcheck

2. Shortening of the Chromosomes with each replication 2. Shortening of the Chromosomes with each replication. Each lagging strand end loses some DNA with each replication. After the very last RNA primer has been removed, there is no 3’ end to add nucleotides too. So a short section of DNA is not replicated and some information is lost. To compensate, each chromosome is capped with TELOMERES – sections of non-sense DNA that don’t code for proteins. Once the telomeres have been worn down, important DNA information begins to get lost. The shortening of telomeres is one of the causes of aging. Cells enter senescence  Don’t divide anymore.

Figure 16.18 End of parental DNA strands Leading strand Lagging strand Last fragment Previous fragment RNA primer Removal of primers and replacement with DNA where a 3 end is available Primer removed but cannot be replaced with DNA because no 3 end available for DNA polymerase Second round of replication New leading strand New lagging strand 5 Further rounds Shorter and shorter daughter molecules 5 3

Differences in Prokaryotes and Eukaryotes Prokaryote chromosomes are circular. Don’t need telomeres