DNA Flashcards
DNA: a phosphate group + deoxyribose + an organic base
nucleic acids are made up of lots of nucleotides joined together by phosphodiester bonds
DNA is a double helix (2 polynucleotides wound round each other)
4 bases: Adenine = Thymine Guanine = Cytosine ∙DNA has a sugar phosphate back bone ∙bases are joined together by H+ bonds ∙strands are antiparallel: 5-3, 3-5
RNA: a phosphate group + ribose + an organic base ∙single stranded ∙4 bases: Adenine = Uracil Guanine = Cytosine There are 3 types of RNA involved in protein synthesis ∙mRNA ∙tRNA ∙rRNA
mRNA: synthesised in the nucleus and carries the genetic code from the DNA to ribosomes in the cytoplasm
tRNA: molecules of tRNA transport specific amino acids to the ribosomes in protein synthesis
rRNA: found in cytoplasm, binding site for tRNA, site of translation
Eukaryotes vs Prokaryotes:
E= DNA enclosed in nucleus
Diploid
chromosomes in pairs
P= no nucleus
DNA loose in cytoplasm
Haploid
∙the genetic code is a triplet code, 3 bases code for 1 amino acid
∙each section of DNA is called a gene
Exons and introns:
∙in eukaryotes the pre-mRNA version of the code is much longer than the final mRNA and contains sequences of bases that need to be removed
∙introns are cut out using endonucleases, not translated
∙the sequence left are called exons, they are spliced together with ligases. this produces the final mRNA
DNA replication:
∙semi conservative= each strand in the double helix acts as a template for the synthesis of a new complementary strand
this process takes us from one starting molecule to two daughter molecules
∙replication always starts at sites called ‘origins of replication’. specialised proteins recognise the origins, bind to this site and open up the DNA
∙as the DNA opens, 2 Y shaped replication forks form, together making up whats known as the ‘replication bubble’
∙DNA helicase is the first replication enzyme to load on at the origin of replication. Helicase breaks hydrogen bonds between the bases
∙proteins called ‘single stranded binding proteins’ coat the seperated strands of DNA near the replication fork, keeping them from re-forming a double helix
Primers and primase:
∙DNA polymerases only add nucleotides to the 3’ end of the DNA
primase makes a RNA primer that provides a 3’ end so DNA polymerase can work on it
Leading and lagging strands:
∙DNA polymerase can only make DNA in the 5-3 direction. As the strands are anti-parallel, both strands need to be made separately
∙5-3 towards the fork is made easily because DNA polymerase is moving in the same direction as the replication fork (LEADING STRAND)
∙5-3 away from the fork is made in fragments, because DNA polymerase is moving in the opposite direction to the fork, so it must come off and re-attach
OKAZAKI FRAGMENTS: fragments named after the Japanese scientist who discovered them
the lagging strand needs a new primer for each fragment
FINALLY:
RNA primers are removed and replaced by DNA
The nicks that remain after the primers, are replaced and get sealed by the enzyme DNA ligase