10th March - Therapies, mRNA export Flashcards
What is morpholino?
A treatment for duchenne’s muscular dystrophy.
It is an oligonucleotide, in which the DNA bases are attached to a backbone of methylenemorpholine rings, which promotes skipping of exon 51
How can pro-apoptotic isoforms of Bcl-X and Mcl-1 be promoted?
Using oligonucleotides which block the anti-apoptotic splice site and enhance apoptosis,
What is the problem with using oligonucleotides in treatment in early tumours?
Delivery as there is no vascular network
What causes spinal muscular dystrophy?
Mutation in SMN1
Why does a mutation in SMN1 cause spinal muscular dystrophy, when everyone carries another copy of SMN, SMN2?
1 base change in SM2 means that 90% of transcripts have exon 7 spliced out, making the resultant protein useless
How could splicing be restored of SMN2 exon 7?
Solution 1.
- -An oligonucleotide that would anneal to the splice site with an RS tail that would bind SRSF1.
- -This worked in vitro
- -However such a long nucleic acid sequence would be difficult to deliver to the tissue
Solution 2.
- -Block a silencer using oligonucleotides
- -Approves as Spinraza in 2017 but had to stop phase II trail early due to failure of placebo
- -Injected oligos into CNS, lasted for about 6 months
Outline Palacino’s 2015 experiment
Screened 1.4 million compounds on SMN2 using a reporter system
1st assay = Exon inclusion –> luciferase expression
2nd assay = Exon exclusion –> luciferase expression
Used two assays to rule out a global increase in expression
–>Found NVS SM1
-Prolonged SMA model mouse life >35 days
- Interacts with U1snRNA and stabilised interaction with 5’ss of exon 7
What does mutant SF3B1 in cancer promote?
Use of alternative branchpoints
What is the function of SF3B1?
Holds the branch site 50A away from the active site
How can mutant SF3B1 be inhibited in cancer?
Use of certain anti-biotics e.g. sudemycins, pladienolide B
Why do SF3B1 inhibitors work on tumours which do not carry a mutation is SF3B1?
Believed that other oncogenic mutations causes the same changes that are seen in mutant SF3B1
What are the therapeutic benefits of inhibiting SR protein kinase 1?
Prevent SRSF1 activity therefore inhibit angiogenesis
How is the mRNA exported from the nucleus?
The EJC helps to recruit proteins necessary for export from the nucleus.
- -P15 binds to RNA
- -TAP binds to nucleoporin, holding the mRNA at the pore
- -Then is exported in a ‘ratcheting’ fashion, similar to a zip tie, in which it accidentally moves forward through natural oscillation and then can’t move back