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Bio - Unit 3

3.1-3.3

TermDefinition
DNA's primary role ensure genetic continuity of a species
Process of going from DNA to protein gene that codes for protein needed is activated, DNA code is transcribed into RNA molecule, RNA moves from nucleus to cytosol and is translated by ribosomes into amino acid chains
genes specific coding regions of DNA that contain instructions for building proteins
DNA packaging in ekaryotes - stored in nucleus - DNA strand wrapped around histones -DNA-histone complexes coil into chromatin fibres - packaging protects and condenses DNA volume
DNA packaging in prokaryotes - located in cytosol - DNA is concentrated in the nucleid
plasmid DNA -small, circular loops of DNA
semiconservative replication model each of the two new DNA molecules consist of one old strand anf one new strand
Process of DNA replication 1. Strand Seperation 2. Building Complementary strands 3. Proofreading and repair
Strand Separation (in dna replication) -begins at replication origin -helicase unwinds dna double helix by breaking h bonds -seperation creates a replication fork -replocation bubble is formed by seperation occuring in btoh directions
solving tension -topoisomerase cuts both or one strand, allowing them to untangle and then rejoining them
solving annealing -seperated strand tend to rejoin - single-strand binding proteins attach to strands to keep them seperated
building complementary strands (in dna replication) -DNA polymerase builds the new strands -new nucleotides are added as DNTPs -hydrolysis of two phosphate groups provides energy to form phosphodiester bond -new strand is always built 5'-3'
the primer problem -dna polymerase can only elongate an existing strand -rna primase builds an rna primer that is complementary to the template strand -this provides a 3' end for dna ploymerase to attach to
leading strand -strand is built towards the replication fork -new strand is synthesized in the 5'-3' direction by dna polymerase III -rna primer only required at the beginning
lagging strand -strand is built away from the replication fork, synthesized discontinuosly -rna primase adds multiple primers dna polymerase III builds strands in short segments (okazaki fragments) -dna polymerase I removes rna primers and adds nucleotides -dna
proofreading (in dna replication) -dna polymerase III proofreads -if incorrect nucleotide is corrected it will be removed and replaced
repair (in dna replicaiton) -dna pol I and II scan dna for errors missed by dna pol III -mismatched bases distort double helix shape -they scan for distortion, cut it out, usesa dna pol to fill gap, dna ligase seels it
Created by: gracie.elisabeth
 

 



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