lecture 5 recapn Flashcards

1
Q

the NF-kB, p53 and HIF pathways all

A

allow the cell/organism to respond to environmental threats

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2
Q

NF-kB is a family of how many proteins

A

5

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3
Q

NF-kB forms dimer complexes which allows them to bind to

A

DNA

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4
Q

rel homology domain is present in all NF-kBs facilitates what

A

the dimeric complexes forming

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5
Q

RelA, RelB and c-rel form a

A

subfamily

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6
Q

transactivation domains allow them to work as what

A

potent activators of genes

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7
Q

p105 and p100 are precursors of which NF-kBs

A

p50 and p52

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8
Q

ubiquitin chains are bound to target protein by

A

E1, E2 or E3 ligases

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9
Q

NF-kB is induced by:

A

inflammatory cytokines
bacterial products
viral proteins and infection
DNA damage
cell stress

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10
Q

NF-kB regulates

A

immune response
stress responses
cell survival and death
cell proliferation

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11
Q

NF-kB dimers are held in an inactive form in the cytoplasm bound to an inhibitory protein called

A

IkB

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12
Q

activation of NF-kB
what is an example of a ligand binds to receptor on cell surface

A

TFNa

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13
Q

binding signals a cascade which results in

A

activation of the IkB kinase complex

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14
Q

what does this complex phosphorylates

A

IkB

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15
Q

what does phosphorylation of IkB signal

A

ubiquitination of the IkB freeing NF-kB

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16
Q

NF-kB goes to the nucleus and does what

A

binds to target sequences in promotors or enhancers of the genes they regulate

17
Q

IkB kinase complex is made up of what 3 components

A

NEMO/IKKγ, IKKα or IKKβ

18
Q

the components of the IkB have ______ repeats

A

ankyrin

19
Q

what do ankyrin repeats do

A

bind to NF-kB complex and retain it making it inactive

20
Q

what residue on IkB gets phosphorylated

A

serine residues

21
Q

when NF-kB gets into the nucleus it can be modifies further by

A

kinases, acetylases, phosphatases and more

22
Q

modifications allows them to selectively interact with other proteins eg

A

co repressors / activators which could determine whether we get expression or not

23
Q

p300/CBP is a co activator and can interact with and modify

A

RelA subunit

24
Q

phosphorylation of RelA regulates its ability to interact with p300/CBP as it

A

opens up its structure and allows binding sites to emerge