Positive: the cAMP-CRP complex promotes transcription
Inactivated by hydrolyzing its GTP into GDP
(1, 2, 10, 40)
LacI bounces around the cell until it happens to come across the operator sequence it binds to. If we just had a couple copies of the protein, most of their time would be spent away from the operator and transcription of the operon would not be repressed in the absence of lactose. Having 40 copies ensures that the operator is almost always bound when there is no lactose present.
When expressed, they often have a easily recognizable effect, such as glowing or changing color
No. these RNA will not be translated and thus it doesn't matter if there are stop codons in the middle of it
An inhibitor of MAPKK
An inhibitor of MAPK
An inhibitor of transcription
(just need one)
Cyclins will be expressed if checkpoint criteria are met
It is used to assess bgal activity because the enzyme changes IPTG from colorless to blue
Methyl groups change the shape and chemistry of the major groove, so transcription factors cannot recognize their binding site.
Methylation also recruits HDAC to compact the surrounding DNA .
2. to find where introns and exons are in a gene
3. to find out if alternative splicing is occurring
4. to find out which genes are typically transcribed in a cell and at what relative levels
5. can compare sequence to other known protein coding sequences in order to hypothesize about the gene's function
Define: the last protein in the chain, the one that carries out the direct action that the signal was intended to produce
Example: the regulatory transcription factor phosphorylated by MAPK
G1 (aka G1/S): Cell must be big enough to divide, have enough nutrients, have undamaged DNA, and receive signals to divide
G2: Make sure chromosomes are done replicating and DNA is undamaged
M: make sure chromosomes are attached to spindle
The bacterium S. lc uses the molecule pizza as a primary food source and cupcake as a secondary food source if pizza is not present. Explain how to conduct a genetic screen using replica plating to find bacteria that have a mutation in their pizza metabolism genes.
1. Mutagenize bacteria / introduce random mutations to bacterial genome
2. plate/grow bacteria on cupcake only media
3. use replica plating to transfer some bacteria to pizza only media
4. observe which colonies grow and which do not
5. colonies that grow on cupcake but not pizza must have a mutation in their pizza metabolism genes.
RNA-binding proteins bound to the UTR may promote or prevent degradation of the mRNA
Can target mRNA from retrotransposon in cytoplasm and degrade it
Can find location of retrotransposon in genome and cause sequence to be methylated
When cell responds to a single signal in multiple ways
For example, maybe MAPKK could phosphorylate MAPK and promote changes in gene expression that cause cell proliferation (as usual) AND ALSO phosphorylate/activate a protein that promotes [insert other reasonable effect]
Phosphorylates proteins associated with
1. chromatin to cause condensation
2. nuclear lamins to cause nuclear envelope breakdown
3. microtubule proteins to activate the spindle
4. Ubiquitin ligase, leading to degradation of cyclin, so it can effectively turn itself off