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{{Team:Paris_Saclay/project_header|titre=CRISPR/Cas9 system}}
 
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=The CRISPR/Cas9 system: a kind of engineer nuclease=
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=The CRISPR/Cas9 system: a very special member of the engineered nucleases family=
  
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Programmable nucleases produce site-specific DNA double-strand breaks (DSBs). These DSBs are then repaired by two endogenous mechanisms: homology-directed repair (HDR) with the presence of a gene targeting vector or a homologous donor DNA, or non-homologous end-joining (NHEJ) without complementary DNA.  These two mechanisms have several consequences: small insertions-deletions (INDEL) in the case of NHEJ repair, substitution, gene disruption, insertion, correction and chromosomal rearrangements in the case of HDR repair. The outcome of genome editing using programmable nucleases are represented on '''Fig. 1''' (Kim & Kim, 2014).
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Programmable nucleases produce site-specific DNA double-strand breaks (DSBs). These DSBs are then repaired by two endogenous mechanisms: homology-directed repair (HDR) with the presence of a gene targeting vector or a homologous donor DNA, or non-homologous end-joining (NHEJ) without complementary DNA.  These two mechanisms have several consequences: small insertions-deletions (INDEL) in the case of NHEJ repair, substitution, gene disruption, insertion, correction and chromosomal rearrangements in the case of HDR repair. The outcome of genome editing using programmable nucleases are represented in '''[Fig. 1]''' (Kim & Kim, 2014).
  
 
[[File:Paris_Saclay--CRISPR1.png|500px|center|]]
 
[[File:Paris_Saclay--CRISPR1.png|500px|center|]]
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<center>'''Figure 1''' : Outcomes of genome editing using endineered nuclease</center>
  
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In the field of biotechnology, three applications are particularly interesting. The first one if gene disruption – gene knock out - ('''Fig. 1A''' – small INDEL) through error-prone NHEJ. INDELs often cause frameshifts in the coding region, which disrupt genetic information and result in gene knock out. The second one is gene insertion – knock in – ('''Fig. 1A''' – gene or tag insertion) through HDR. To achieve this, the nuclease is co-transfected with a targeting vector, in which the genetic segment to be incorporated is flanked by homology arms with sequences that are identical to those near the target region. The last one is gene correction and point mutagenesis ('''Fig. 1A''' – gene correction or point mutagenesis) through HDR. Point mutations can be corrected or single-nucleotide variations (SNP) introduced in the genome through co-delivery of programmable nucleases and targeting vectors or single-strand oligodeoxynucleotides (ssODNs). The chromosomal rearrangements ('''Fig. 1B & '''Fig. 1C''') are not very used in crop improvement, but have a therapeutic interest for chromosomal diseases (Kim & Kim, 2014).
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In the field of biotechnology, three applications are particularly interesting. The first one is gene disruption – gene knock out ('''[Fig. 1A]''' – small INDEL) - through error-prone NHEJ. INDELs often cause frameshifts in the coding region, which disrupt genetic information and result in gene knock out. The second one is gene insertion – knock in ('''[Fig. 1A]''' – gene or tag insertion)- through HDR. To achieve this, the nuclease is co-transfected with a targeting vector, in which the genetic segment to be incorporated is flanked by homology arms with sequences that are identical to those near the target region. The last one is gene correction and point mutagenesis ('''[Fig. 1A]''' – gene correction or point mutagenesis) through HDR. Point mutations can be corrected or single-nucleotide variations (SNP) introduced in the genome through co-delivery of programmable nucleases and targeting vectors or single-strand oligodeoxynucleotides (ssODNs). The chromosomal rearrangements '''[Fig. 1B & Fig. 1C'''] are not very used in crop improvement, but have a therapeutic interest for chromosomal diseases (Kim & Kim, 2014).
  
 
=Structure of CRISPR/Cas9=
 
=Structure of CRISPR/Cas9=
  
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Ishino et al. reported in 1987 the presence of an intriguing stretch of DNA, close to a bacterial protein gene and composed of short direct-repeats interspaced by short unique sequences (protospacers) in E. coli genome, coming from bacteriophages of plasmids. The Cas protein is an endonuclease involved in a bacterial defense mechanism against bacteriophages by DSB. This is the work of Emmanuelle Charpentier’s teams between 2011 and 2012, by describing the molecular mechanism governing the accurate positioning of the DSB in DNA in the natural CRISPR/Cas9 system, which lead to the construction of artificial CRISPR/Cas9 engineered to produce DSB at any position chosen along the DNA sequence (Quétier, 2016). This DSB is induced in a specific way by an sgRNA, that is way the CRISPR/Cas9 system is considered as a RGEN (RNA-guided engineered nuclease), which a representation is given on '''Fig. 2'''.
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Ishino et al. reported in 1987 the presence of an intriguing stretch of DNA, close to a bacterial protein gene and composed of short direct-repeats interspaced by short unique sequences (protospacers) in <i>E. coli</i> genome, coming from bacteriophages of plasmids. The Cas protein is an endonuclease involved in a bacterial defense mechanism against bacteriophages by DSB. This is the work of Emmanuelle Charpentier’s teams between 2011 and 2012, by describing the molecular mechanism governing the accurate positioning of the DSB in DNA in the natural CRISPR/Cas9 system, which lead to the construction of artificial CRISPR/Cas9 engineered to produce DSB at any position chosen along the DNA sequence (Quétier, 2016). This DSB is specific thanks to the presence of the sgRNA, which is why the CRISPR/Cas9 system is considered as a RGEN (RNA-guided engineered nuclease). A representation is given on '''[Fig. 2]'''.
  
 
[[File:Paris_Saclay--CRISPR2.png|500px|center|]]
 
[[File:Paris_Saclay--CRISPR2.png|500px|center|]]
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<center>'''Figure 2''' : Structure of CRISP/Cas9 system</center>
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Bacteria insert protospacers into their own genome to form a CRISPR (clustered regularly interspaced short palindromic repeats). In type II CRISPR systems, the transcription of a CRISPR unit leads to a RNA called crRNA, which binds by complementary in 3’ to an other RNA in 5’, called tracrRNA. Once these two RNA are complexed, the new structure called sgRNA is blocked in the catalytic site of the Cas9 protein, to form an active DNA endonuclease, which is often termed dualRNA–Cas9. This complex can bind to DNA and recognize a 23bp target DNA sequence that is composed of the 20bp guide sequence in the crRNA (the protospacer) and the 5’-X20NGG-3’ sequence known as protospacer adjacent motif (PAM), which is recognized by Cas9 itself (Kim & Kim, 2014).
+
Bacteria insert protospacers into their own genome to form a CRISPR (clustered regularly interspaced short palindromic repeats). In type II CRISPR systems, the transcription of a CRISPR unit leads to a RNA called crRNA, which binds by complementary in 3’ to an other RNA in 5’, called tracrRNA. Once these two RNAs are complexed, the new structure called sgRNA is blocked in the catalytic site of the Cas9 protein, to form an active DNA endonuclease, which is often termed dualRNA–Cas9. This complex can bind to DNA and recognize a 23bp target DNA sequence that is composed of the 20bp guide sequence in the crRNA (the protospacer) and the 5’-X20NGG-3’ sequence known as protospacer adjacent motif (PAM), which is recognized by Cas9 itself (Kim & Kim, 2014).
  
 
=References=
 
=References=

Latest revision as of 15:18, 19 October 2016

CRISPR/Cas9 system

The CRISPR/Cas9 system: a very special member of the engineered nucleases family

Programmable nucleases produce site-specific DNA double-strand breaks (DSBs). These DSBs are then repaired by two endogenous mechanisms: homology-directed repair (HDR) with the presence of a gene targeting vector or a homologous donor DNA, or non-homologous end-joining (NHEJ) without complementary DNA. These two mechanisms have several consequences: small insertions-deletions (INDEL) in the case of NHEJ repair, substitution, gene disruption, insertion, correction and chromosomal rearrangements in the case of HDR repair. The outcome of genome editing using programmable nucleases are represented in [Fig. 1] (Kim & Kim, 2014).

Paris Saclay--CRISPR1.png
Figure 1 : Outcomes of genome editing using endineered nuclease


In the field of biotechnology, three applications are particularly interesting. The first one is gene disruption – gene knock out ([Fig. 1A] – small INDEL) - through error-prone NHEJ. INDELs often cause frameshifts in the coding region, which disrupt genetic information and result in gene knock out. The second one is gene insertion – knock in ([Fig. 1A] – gene or tag insertion)- through HDR. To achieve this, the nuclease is co-transfected with a targeting vector, in which the genetic segment to be incorporated is flanked by homology arms with sequences that are identical to those near the target region. The last one is gene correction and point mutagenesis ([Fig. 1A] – gene correction or point mutagenesis) through HDR. Point mutations can be corrected or single-nucleotide variations (SNP) introduced in the genome through co-delivery of programmable nucleases and targeting vectors or single-strand oligodeoxynucleotides (ssODNs). The chromosomal rearrangements [Fig. 1B & Fig. 1C] are not very used in crop improvement, but have a therapeutic interest for chromosomal diseases (Kim & Kim, 2014).

Structure of CRISPR/Cas9

Ishino et al. reported in 1987 the presence of an intriguing stretch of DNA, close to a bacterial protein gene and composed of short direct-repeats interspaced by short unique sequences (protospacers) in E. coli genome, coming from bacteriophages of plasmids. The Cas protein is an endonuclease involved in a bacterial defense mechanism against bacteriophages by DSB. This is the work of Emmanuelle Charpentier’s teams between 2011 and 2012, by describing the molecular mechanism governing the accurate positioning of the DSB in DNA in the natural CRISPR/Cas9 system, which lead to the construction of artificial CRISPR/Cas9 engineered to produce DSB at any position chosen along the DNA sequence (Quétier, 2016). This DSB is specific thanks to the presence of the sgRNA, which is why the CRISPR/Cas9 system is considered as a RGEN (RNA-guided engineered nuclease). A representation is given on [Fig. 2].

Paris Saclay--CRISPR2.png
Figure 2 : Structure of CRISP/Cas9 system


Bacteria insert protospacers into their own genome to form a CRISPR (clustered regularly interspaced short palindromic repeats). In type II CRISPR systems, the transcription of a CRISPR unit leads to a RNA called crRNA, which binds by complementary in 3’ to an other RNA in 5’, called tracrRNA. Once these two RNAs are complexed, the new structure called sgRNA is blocked in the catalytic site of the Cas9 protein, to form an active DNA endonuclease, which is often termed dualRNA–Cas9. This complex can bind to DNA and recognize a 23bp target DNA sequence that is composed of the 20bp guide sequence in the crRNA (the protospacer) and the 5’-X20NGG-3’ sequence known as protospacer adjacent motif (PAM), which is recognized by Cas9 itself (Kim & Kim, 2014).

References

Kim H, Kim J-S. A guide to genome engineering with programmable nucleases. Nature Reviews Genetics. 2 avr 2014;15(5):321‑34. http://www.nature.com/nrg/journal/v15/n5/full/nrg3686.html

Quétier F. The CRISPR-Cas9 technology: Closer to the ultimate toolkit for targeted genome editing. Plant Science. janv 2016;242:65‑76. http://www.sciencedirect.com/science/article/pii/S0168945215300613





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