CMB2000/L13 CRISPR-CAS9 Flashcards

1
Q

What does CRISPR-CAS9 stand for?

A

Clustered Regulatory Interspaced Short Palindromic Repeats and CRISPR Associated Proteins

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2
Q

What are the 3 components of CRISPR-CAS9?

A

Cas9 - protein component
crRNA - RNA component
tracrRNA - RNA component

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3
Q

What does the CRISPR-CAS9 complex do?

A

Cleaves invading DNA to prevent re-infection by viruses

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4
Q

How does CRISPR act as an adaptive immune regulator? (2)

A
  1. Invading DNA recognised and cut by Cas1-2 into fragments (protospacers)
  2. Protospacers integrated into CRISPR locus in bacterial genome
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5
Q

Describe what occurs upon viral reinfection with CRISPR. (4)

A

Transcription of protospacers activated
Bind to Cas9
Cas9/RAN duplex recruited to complementary sequence on invading DNA
Cas9 cuts DNA strands creating double strand break to prevent infection

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6
Q

Describe the structure of the CRIPSR locus. (4)

A

5’ transactivating RNA
Cas operon encoding Cas components
Identical repeat arrays
Spacers of invading DNA

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7
Q

What is the guide RNA (gRNA)?

A

Complex formed between transactivating RNA (tracrRNA) and protospacer/CRISPR RNA (crRNA)
Enables selective binding of Cas9 to invading DNA sequences

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8
Q

Explain how protospacer adjacent motifs (PAM) allow Cas9-mediated DNA cleavage.

A

Cas9 will not cut invading DNA without PAM site irrespective of Cas/gRNA binding

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9
Q

Describe the location of protospacer adjacent motifs.

A

2-8 base pair sequence 3-4 base pairs downstream of cut site

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10
Q

Give the 2 steps of Cas9 function in initial infection.

A

Protospacer aquisition
Spacer integration

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11
Q

Give the 4 steps of Cas9 function in re-infection.

A

Transcription
Binding to Cas9
Sequence comparison
Cleavage

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12
Q

How is gRNA modified for biomedical studies?

A

Linking cRNA and tracrRNA by adding linker loop
= composite gRNA

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13
Q

Give 2 properties of correct gRNA design.

A

Contains protospacer sequence (target sequence) upstream of PAM site
Should be selective to a single genome locus to avoid off target effects

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14
Q

If DNA is damaged by ionising radiation, double stranded breaks are repaired of one of two which mechanisms?

A

Homology-directly repair (HDR)
Non-homologous end-joining (NDEJ)

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15
Q

Describe how non-homologous end-joining (NHEJ) enables error-prone DNA repair. (3)

A

Introduces insertions or deletions into DNA
Impacts gene function
Often results in premature stop codons

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16
Q

Describe how homology-directed repair (HDR) enables precise DNA repair.

A

DNA precisely repaired using sister chromatid during S phase of cell cycle
Key to CRISPR knock-in studies

17
Q

Give the 3 steps to homology-directed repair after a double-strand break.

A

End resection
Strand invasion synthesis
Synthesis-dependent strand annealing

18
Q

Describe CRISPR-mediated gene knockout via NHEJ. (5)

A

Target Cas9:gRNA complex to gene of interest
DSB introduced
Cell repairs break via error-prone NHEJ
Indels introduced generate frameshift
Normal gene product not expressed

19
Q

Describe CRISPR-mediated gene knock-in via HDR. (5)

A

DSB introduced by Cas9-gRNA complex
Template introduced for use in repair
HDR template requires >60bp homology arms of either side of mutation/insert
PAM sites removed from HR template to prevent re-targeting of region
Inserts several kilobases possible

20
Q

Explain which receptor signalling is the main driver of prostate cancer. How is this useful in treatment?

A

Androgen receptors (AR)
Current treatment aims to inactivate AR by blocking ligand binding

21
Q

What is castrate-resistant prostate cancer?

A

Relapsed, incurable prostate cancer

22
Q

What 2 CRISPR-based studies are there for prostate cancer?

A

Generate Cas9-expressing prostate cancer cell line to knock-out AR
Create modified prostate cancer cell line to study function of aberrant forms of AR

23
Q

Describe what studies of androgen receptor variants have discovered so far. (2)

A

Alternative splicing principally involved in generation of AR-Vs in response to AR-targeting agents
Lack exons 4-8 encoding ligand-binding domain (LBD)
Loss of AR LBD creates constitutively active transcription factors refractory to enzalutamide
Expression of AR-Vs elevated in advanced disease

24
Q

Why is it difficult to study AR-Vs in isolation?

A

CWR22Rv1 cell line expresses both full length AR and AR-Vs
Full length AR (FL-AR) encoded by exons 1-8
AR-V7 lacks exons 4-8 giving shorter protein

25
How is CRISPR hoped to cure prostate cancer? (2)
Block expression of full length AR gRNA designed to exon 5 of AR HDR template with point mutation encodes stop codon & stop formation of FL-AR
26
Describe CWR22Rv1-AR-EK. (3)
First ever CRISPR knock-in prostate cancer cell line worldwide Characterised how AR-Vs work by studying in isolation Defined therapeutic vulnerability in prostate cancer cells expressing AR-Vs involving protein PARP1/2
27
Give 3 considerations of cell therapy.
Efficacy of delivery Regulatory guidelines Mosaicism Specificity Immunogenicity Germline vs somatic
28
Describe ex-vivo delivery of CRISPR in the clinic. (4)
Remove cells from patient/donor Edit genome Screen/expand cell populations Engraft cells back into patient
29
Describe in-vivo delivery of CRISPR in the clinic. (2)
Package CRISPR/Cas in a delivery vehicle Deliver to patient
30
Describe the potential of CRISPR editing for HIV treatment.
Homozygous CCR5^32 donor gave stem cell transplant Patient/recipient no longer required anti-viral therapy
31
Describe how modified CCR5 results in a resistance to HIV infection.
Modified CCR5 means virus cannot bind to receptor and infect cells 32bp deletion results in frameshift and unstable protein
32
Describe how successful CRISPR editing of CCR5 in vivo confers HIV-1 resistance.
Long term CCR5 disruption observed CCR5 disrupted HSCs were able to reconstitute function immune system Viral titre reduction and increase CD4+ T cells demonstrated HIV resistance
33
Explain how CRISPR editing of CCR5 gene applies in humans.
Donor CCR5 wild-type gave stem cells CRISPR used to disrupt CCR5 in donated HSCs CCR5 ablated cells persisted for >19 months Low amounts of modified cells means no HIV resistance