DNA Replication - Tut Group Case 2 (DNA/RNA)

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Summary

This document summarizes the process of DNA replication, outlining the steps involved and the role of various enzymes. It also compares and contrasts DNA replication in eukaryotic and prokaryotic cells. The document also touches on crucial components like the replication fork, Okazaki fragments, and the functions of different polymerases.

Full Transcript

**DNA replication** - Where does replication take place in cell cycle? - late G1/ mostly S-phase of the interphase 1. *the replication* - **The adding of the complementary bases :** - **Okazaki-fragments** 2. *finishing the replication* 3. *telomerase* - **Store genetic informat...

**DNA replication** - Where does replication take place in cell cycle? - late G1/ mostly S-phase of the interphase 1. *the replication* - **The adding of the complementary bases :** - **Okazaki-fragments** 2. *finishing the replication* 3. *telomerase* - **Store genetic information** - **Replication** - **Gene expression** - **Genetic variation** - Mutations + recombination happen during DNA replication - Simple structure nucleotide DNA = phosphate-sugar (deoxyribose)-nitrogenous base (A,T,C,G) Pyrimidines= 1 carbon nitrogen bases (2N) Purines= 2 carbon nitrogen ring bases (4 N) =\> step ladder model - Sugar phosphate backbone + base pairs - Formation sugar phosphate backbone ![](media/image5.png) Phosphor= connected to 2 sugars -\>3' sugar above -\>5' sugar below = phosphodiester bonds (this strand=5'-3' direction) 5'=phosphate end 3'=-OH end \-\-\-\--opposite strand runs in other direction [=anti-parallel ] =\>double helix structure 2 strands -\>hydrogen bonds (easy to break during replication) DNA = chiral molecule -\>left(-)- and right(+) handed double-helix -\>reality= b-DNA , z-DNA, a-DNA =\>major/minor groove Major groove =\>bigger gap between sugar phosphate backbone Minor groove =\>smaller gap '' =\>ratio: \~1.8 = considered pure DNA Rotation of the phosphor during binding= cause rotation 10-11 turns in helix DNA turn=clockwise **DNA packaging in prokaryotic and eukaryotic cells** 1. Eukaryotic cells =\>DNA wrapped around histones to pack in smaller spaces [Histones + DNA = chromatin ] Histones=building blocks [nucleosomes] (nucleosomes=when under microscope the beads in the necklace(chromatin strand)) Nucleosome=octamer histones + DNA wrapped around DNA=wrapped around octamer of histones = important during condensing DNA -\>cell nuclear division Building histones=\>4 types proteins (h3, h4, h2a, h2b) =\>form dimer 2x h3,h4 dimer = tetramer + 2x h2a,h2b dimer =\>result =8 proteins form octamer Histones + part Dna= - = ionic bond =\>charge -H1 histone-\> packages it together =\>makes it more condensed -after DNA wrapped around histones=\>chromatin looping + condensation 2. Prokaryotic cells =\>supercoiling (-=opp.direction double helix/+=same direction double helix) supercoiling) -\>*how to decide?* =\>2 major topoisomerases indicate supercoiling and relax supercoiling (gyrase-\>negative supercoils in relaxed DNA + relax positive coils) (topoisomerase 1 -\>relaxes neg\> coiled DNA ) Tension that comes from major/minor groove DNA =\>causes the DNA to coil **DNA and ATP -\>sugar phosphate backbone + connecting bases** ATP = nucleotide with 3 phosphate groups (adenine + sugar + triphosphate) *Synthesis of the sugar phosphate backbone* Backbone = polymer -\>monomer to polymer=phosphorylation ATP -3P= AMP (nucleotide in DNA )+ energy released ! also with the nucleosides-\>have 3 phosphate groups other bases (TTP, GTP, CTP) *Replication*=\> DNA polymerase III connects nucleoside (3 phosphate groups) to correct base-\> 2 phosphate break off = release of energy to make bond between bases **=\>extra information : give the written description of the leading strand and lagging strand (definition) then=\>review the structure of the double replication fork (where is the leading and where is the lagging if you have a double replication fork)** The leading strand is continuously extended from the primer by a DNA polymerase with high [processivity](https://en.wikipedia.org/wiki/Processivity), while the lagging strand is extended discontinuously from each primer forming [Okazaki fragments](https://en.wikipedia.org/wiki/Okazaki_fragments). **=\>functions of polymerase I, II, III** Pol I =\>DNA polymerase I functions to fill DNA gaps that arise during DNA replication, repair, and recombination Pol II =\> DNA polymerase II also functions in editing and proofreading mainly in the lagging strand  Pol III =\> DNA polymerase III is the main replicative enzyme.

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