5 Gene Expression Flashcards
Genes produce proteins
This idea pre-dates DNA structure —> Beadle and Tatum (19410 - mutations in Neurospora crassa can be localised to particular point on chromosome —> correlate with defects in particular enzymes)
Central dogma (Crick) = image below
Genetic Code
Genetic code - no punction / non-overlapping / universal
DNA adapted - changing the 3rd base in a codon often has no effect on the AA coded for
Genetic code is non-random —> adapted for resistance to change but is now fixed
First position changes result in similar chemistry
Bacterial DNA
Packaged by supercoiling and wrapping round some proteins / fairly open structure / default position is that genes are on - transcribed / circular DNA
RNA polymerase
- Core polymerase —> sigma proteins —> holoenzyme
Genes and promoters
RNA polymerase recognised promoter, unwinds due to the A-T binds (weaker than c-G becayse AT onky have 3 H bonds) sites and starts RNA resytnetisis at +1
Synthesising 5’-3’ that’s complementary to template stand —> unwinds 15 bases at a time roughly
Control of gene expression - simplest way for a repressor protein to work
bind to DNA and prevent RNA polymerase transcription which is negative regular
Control of gene expression - positive regulators
enhance the amount of transcription occurring
Control of gene expression - tRNA adapters
tRNA adapters - Anticodon - recognises codon by complimentary base pairing —> attach relative AA
Ribosome structure
half of its mass is ribosomal RNA and it’s AT is made of RNA = ribozyme
Ribosome has 2 subunits and 3 possible binding sites
Chemistry of translation
Adjacent slots, bring together 2 tRNAs and therefore 2 AA corresponding to the codons, theyre close enough that the enzyme can then catalyse the reaction between the amino group of 1 AA to the carboxyl group of another AA which is attached to the tRNA which eliminates the tRNA and the 2 join together —> peptide bond
When stop codons reached a different protein binds
Eukaryotic gene expression
Transcription (nucleus) and translation (cytoplasm) occur in separate places + separate times
Message is processed —> capping, poly-A tail, splicing
Chromatin structure - 1st level of control
Chromatin organisation
DNA wrapped around histones to make nucleosomes / wrapped into 30nm fibre / most DNA wrapped in fibres for a majority of the time —> major level of control based on how tightly packaged the genes are = DNA accessibility
Eukaryotic gene expression - DNA accessibility
if theres a methyl group on the CG that’s a marker that the DNA should stay packaged (marker of inactive DNA)
Eukaryotic gene expression - histone modifications
methylation (tighter) and acetylation (less tight)
Eukaryotic gene expression - chromatin remodelling
ATP dependant / nucleosome sliding / displacement = exposes part of DNA
When does eukaryotic transcription occur
Only present when certain proteins are present (highly regulated)
Eukaryotic message processing
3’ the end gets truncated —> helps with recognition (sacrificial extension that can be removed without damaging mRNA)
Splicing
snRNPs serve to find the boundaries between exons and introns by base pairing and facilitate the removal of introns - in nucleus
Alternative splicing
Genes can produce multiple related proteins
90% human genes may be alternatively spliced