1. CRISPR Flashcards

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1
Q

what is CRISPR

A

allows scientists to precisely edit the DNA of organisms by making targeted changes to their genetic code.

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2
Q

what was the “traditional” genome editing

A
  • cut the target
  • add modification
  • new genomic sequence
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3
Q

what are some applications of gene editing

A

Agriculture: gene editing can be used to design crops with desirable traits

Biomedicine: can treat genetic disorders by correcting gene causing mutations

Drug discovery and development

Livestock improvement

Biofuel production

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4
Q

Zinc finger Nucleases: what is it

A

Zinc Finger Nucleases (ZFNs) are like tiny scissors that scientists use to cut specific parts of DNA.

By cutting the DNA at a specific spot, scientists can then make changes to the DNA sequence.

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5
Q

when are zinc Finger Nucleases used

A

This technology was used before CRISPR came along and is still used in some cases where very precise editing is needed

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5
Q

what are the two parts of Zinc Finger Nucleases

A

Zinc Finger Domains: They are designed to recognize and attach to specific sequences of DNA.

Nuclease Domain: cuts the DNA at the specific location

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6
Q

TALE Nucleases

A

DNA-cutting protein used in genome editing
create targeted double-stranded breaks in DNA

TALEs recognize a specific sequence of DNA, nucleases cut the DNA in a specific location allowing researchers to edit the genetic code

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7
Q

what does CRISPR stand for

A

clustered regularly interspaced short palindromic repeats

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8
Q

bacterial immunity

A

the bodies ability to defend itself again bacterial infections

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9
Q

immunization

A

process by which a person is made immune or resistant to an infectious disease by administering a vaccine

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10
Q

CRISPR targeting

A

Cas9 is guided to the desired location by gRNA

Cas9 then makes targeted cuts in the DNA at specific locations

once the DNA is cut the cell’s natural repair mechanisms come into play

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11
Q

protein based genome editing

A

protein and DNA interface is very complex

construction is relatively expensive and complicated

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12
Q

different approaches of exploiting eukaryotic recombination systems to edit genomic DNA

A
  • homology-directed repair
  • non- homologous end joining
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13
Q

explain non-homologous end joining

A

a repair pathway for DNA double strand breaks through direct ligation of the break end without using a homologous template
this is an error prone process and often causes small insertions and deletions

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14
Q

homology directed repair

A

template directed repair of DNA strand bases using homologous DNA sequences

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15
Q

synthetic gene circuits

A

gRNAs can regulate other gRNAs through conventional and synthetic promoters

16
Q

gRNAs in context of CRISPR-Cas 9 gene editing

A

guide RNAs are short RNA molecules that serve as guides to direct the Cas9 enzyme to the desired location in the genome

17
Q

Cas9

A

acts as a molecular scissors that can cut the DNA at the target site specified by the gRNA

18
Q

alternatives to Cas9

A

Cpf1: has “sticky ends”
in contrast to Cas9 which has blunt ended double strand breaks

19
Q

CRISPR and protecting babies

A

CRISPR can make genetic modifications in embryos or gametes to prevent the transmission of genetic diseases from patients to their children.

CRISPR can detect abnormalities in fetal DNA obtained from maternal blood samples allowing for early detection and management of genetic conditions during pregnancy