SUMO Flashcards

1
Q

Define post-translational modifications

A
  • Covalent attachment (isopeptide bond) of a modifier protein after translation of mRNA in an enzymatic process
  • Regulate proteome complexity (5% of proteome is enzymes for ptm)
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2
Q

What is the function of post-translational modifications?

A
  • Ligand binding
  • Trafficking
  • Activation (e.g phosphorylation)
  • Targetting for degradation
  • Facilitating protein-protein interations
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3
Q

Define protein protein interactions

A
  • Physical contact between two or more proteins (non-covalent)
  • Can be transient or long-lived
  • Underpin biochemical properties of proteins
  • Combinations of hydrophobic bonding, salt bridges, van der waals forces and hydrogen bonds
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4
Q

What is the significance of SDS in a western blot?

A
  • Give negative charge

- Prevent protein-protein interactions as it is a strong detergent (does not break covalent interactions)

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5
Q

What are the differences between SUMOylation and ubiquitin?

A
  • E3s are not important and can be done without them
  • Only one type of ubiquitin, different isoforms of sumo
  • Potential for mono-SUMOylation bu SUMO-1 (can also act as chain terminator)
  • Far reduced complexity of system (only 1 E1 and E2, only 4 x E3)
  • Requires motif (consensus site) on target protein
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6
Q

How are the SUMO isoforms formed?

A
  • Produced as longer precursor
  • Cleaved at di-glycine, this glycine used to bond to target proteins on lysine
  • SUMO2/3 are 97% identical
  • SUMO 1 is 40% identiclal
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7
Q

What motif is common in proteins binding to SUMO?

A
FILMV motif (also contained by SUMO-2/3 but nor SUMO-1 which is why it cannot form a chain) 
- Proteins can contain multiple of these sites leading to them becoming heavily modified by SUMO
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8
Q

What is SUMO signalling involved in?

A

Implicated in almost every NUCLEAR process: facilitation of protein-protein interactions

  • Nuclear pore regulation
  • Transcription factor regulation
  • Genomic stability
  • Protein stability
  • Anti-viral/pro-viral response
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9
Q

What is the typical SUMO-interacting motif?

A
  • Hydrophobic domain surrounded by acidic residues (phosphorylation, also believed to mediate isoform specificity)
  • Interacts with SUMO at its second beta sheet
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10
Q

What are PML Nuclear bodies?

A
  • Found within the nuclei
  • Heavily co-localised with SUMO
  • Works as a recruitment domain for many different proteins and can be found around detected virus
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11
Q

How does SUMO aid the function of PML-NBs?

A
  • Post translational modification of SUMO (PMLs have a SIM domain) to form a network and ensuing protein protein interactions to produce PML-associated proteins
  • Often found on viruses in the nucleus
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12
Q

What is the difference between poly and multi SUMOylation?

A

poly - multi-SIM protein interacting with one SUMO
multi - multi-SIM protein interacting with many SUMOs
- Protein with multiple SIM domains can interact with many SUMO-modified proteins

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13
Q

Give an example of SUMO-Ub cross-talk?

A
  • RNF4 is a SUMO-targetted ubiquitin ligase (E3 ligase)
  • Protein that is poly-SUMOylated
  • RNF4 multiple SIM domains, must bind to poly-sumoylayted protein to dimerize
  • Can then target these proteins for degradation
  • This is important for PMLs
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14
Q

What is acute promyelocytic leukaemia?

A
  • Rare but devastating disease
  • Cased by genomic transocation causing PML-RAR fusion
  • Blocks normal myeloid differentiation program as fusion protein is thought to repress genes associated with differentiation
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15
Q

How could APL be treated?

A
  • PML can interact with DNA, can be SUMOylated which can bring in proteins that act as transcription repressors, RAR also acts as a repressor
  • Could be treated through the upregulation of SUMOylation of PML, target for degradation through RNF4 allowing genes to activate again
  • Can be done through treatment with arsenic
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