Test 3 Flashcards
5 mechanisms of transcriptional control
- general transcription factors
- activators
- methylation
- histone tail acetylation
- chromatin remodelling
what are general transcription factors and what do they do?
generate a low level of expression on their own. The more there are, the higher the expression of the gene.
activators
- proteins that bind to the promoter proximal elements and bring a high transcription rate
- others can bind to the enhancer region and form a multi-protein complex with activators at the promoter proximal elements, which brings the maximum rate of expression
methylation
- DNA methylation enzymes add a methyl group to bases of DNA.
- Methylated bases in promoter regions can prevent the binding of transcription factors, turning the gene off
histone tail acetylation
- changes the charge on the histone tails and results in a loosening of the association of the histones with DNA
chromatin remodelling
- chromatin can be remodelled to make the promoter accessible to transcription factors and activators, increasing the transcription rate
3 mechanisms of post transcriptional control
- caping: 5’ cap and poly-a tail
- alternative splicing
5’ cap
- added to 5’ end of mRNA
- protects it from degradation and is the site where ribosomes attach at the start of translation
poly-A tail
the tail prevents mRNA from degradation when they enter the cytoplasm
alternative splicing
- introns removed by spliceosomes
- spliceosomes cleave the pre-mRNA at the junction between the 3’ and 5’ end of intron.
- intron loops back on itself ans is cleaved
- only exons left (introns = non protein coding segments)
mechanism of translational control
adjusting the length of the poly-a tail
adjusting length of poly a tail
- enzymes change the length of the tail
- increased length = increased translation
- decreased length = decreased translation
3 mechanisms of post translational control
- processing (protein activation)
- polyubiquitination (protein degradation)
- proteasome (protein degradation)
processing
- proteins are synthesized as inactive precursors, which are converted to an active form under regulatory control.
- protein activation
polyubiquitination
- short lived proteins are marked for breakdown by enzymes that attach to a doom tag which is called ubiquitin.
- the tag labels the unnecessary or damaged proteins that need to be destroyed.
- addition of ubiquitin to a protein
proteasome
- proteasomes recognize doom tags and attack the protein to break it down
- proteasome = large cytoplasmic complex of different proteins.
why are eukaryotic gene expression more complicated than prokaryotic?
- more complex cells (organelles, different proteins that need to be coded for)
- nuclear DNA is organized in histones (tightly packed DNA) into chromatin
- multicellular eukaryotes produce large numbers and different types of cells
what are promoter proximal elements?
regulatory sequences farther upstream that may stimulate or inhibit the rate of transcription initiation
where do general transcription factors bind?
to promoter in TATA box
what are housekeeping genes?
genes that are expressed in all cell types for basic cellular functions (ex: glucose metabolism)
what is an advantage that eukaryotes have on prokaryotes?
exon shuffling = protein diversity (but can also lead to disorders)
what are the 3 disciplines of evolution?
biogeography
comparative morphology
geology
biogeography
study of geographic distribution of plants, animals and other forms of life
what is comparative morphology
comparing the morphology of species to understand and discover common ancestors