-
Je něco špatně v tomto záznamu ?
Expanding the CRISPR/Cas9 toolkit for Pichia pastoris with efficient donor integration and alternative resistance markers
A. Weninger, JE. Fischer, H. Raschmanová, C. Kniely, T. Vogl, A. Glieder,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29091307
DOI
10.1002/jcb.26474
Knihovny.cz E-zdroje
- MeSH
- CRISPR-Cas systémy MeSH
- genetické inženýrství MeSH
- genetické markery MeSH
- genový knockout metody MeSH
- mutace INDEL MeSH
- oprava DNA spojením konců MeSH
- Pichia genetika růst a vývoj MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Komagataella phaffii (syn. Pichia pastoris) is one of the most commonly used host systems for recombinant protein expression. Achieving targeted genetic modifications had been hindered by low frequencies of homologous recombination (HR). Recently, a CRISPR/Cas9 genome editing system has been implemented for P. pastoris enabling gene knockouts based on indels (insertion, deletions) via non-homologous end joining (NHEJ) at near 100% efficiency. However, specifically integrating homologous donor cassettes via HR for replacement studies had proven difficult resulting at most in ∼20% correct integration using CRISPR/Cas9. Here, we demonstrate the CRISPR/Cas9 mediated integration of markerless donor cassettes at efficiencies approaching 100% using a ku70 deletion strain. The Ku70p is involved in NHEJ repair and lack of the protein appears to favor repair via HR near exclusively. While the absolute number of transformants in the Δku70 strain is reduced, virtually all surviving transformants showed correct integration. In the wildtype strain, markerless donor cassette integration was also improved up to 25-fold by placing an autonomously replicating sequence (ARS) on the donor cassette. Alternative strategies for improving donor cassette integration using a Cas9 nickase variant or reducing off targeting associated toxicity using a high fidelity Cas9 variant were so far not successful in our hands in P. pastoris. Furthermore we provide Cas9/gRNA expression plasmids with a Geneticin resistance marker which proved to be versatile tools for marker recycling. The reported CRSIPR-Cas9 tools can be applied for modifying existing production strains and also pave the way for markerless whole genome modification studies in P. pastoris.
Bisy e U Wetzawinkel Hofstätten Raab Austria
Department of Biotechnology University of Chemistry and Technology Prague Prague Czech Republic
Institute of Molecular Biotechnology Graz University of Technology Graz Austria
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19001119
- 003
- CZ-PrNML
- 005
- 20190122094110.0
- 007
- ta
- 008
- 190107s2018 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1002/jcb.26474 $2 doi
- 035 __
- $a (PubMed)29091307
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Weninger, Astrid $u Institute of Molecular Biotechnology, Graz University of Technology, Graz, Austria.
- 245 10
- $a Expanding the CRISPR/Cas9 toolkit for Pichia pastoris with efficient donor integration and alternative resistance markers / $c A. Weninger, JE. Fischer, H. Raschmanová, C. Kniely, T. Vogl, A. Glieder,
- 520 9_
- $a Komagataella phaffii (syn. Pichia pastoris) is one of the most commonly used host systems for recombinant protein expression. Achieving targeted genetic modifications had been hindered by low frequencies of homologous recombination (HR). Recently, a CRISPR/Cas9 genome editing system has been implemented for P. pastoris enabling gene knockouts based on indels (insertion, deletions) via non-homologous end joining (NHEJ) at near 100% efficiency. However, specifically integrating homologous donor cassettes via HR for replacement studies had proven difficult resulting at most in ∼20% correct integration using CRISPR/Cas9. Here, we demonstrate the CRISPR/Cas9 mediated integration of markerless donor cassettes at efficiencies approaching 100% using a ku70 deletion strain. The Ku70p is involved in NHEJ repair and lack of the protein appears to favor repair via HR near exclusively. While the absolute number of transformants in the Δku70 strain is reduced, virtually all surviving transformants showed correct integration. In the wildtype strain, markerless donor cassette integration was also improved up to 25-fold by placing an autonomously replicating sequence (ARS) on the donor cassette. Alternative strategies for improving donor cassette integration using a Cas9 nickase variant or reducing off targeting associated toxicity using a high fidelity Cas9 variant were so far not successful in our hands in P. pastoris. Furthermore we provide Cas9/gRNA expression plasmids with a Geneticin resistance marker which proved to be versatile tools for marker recycling. The reported CRSIPR-Cas9 tools can be applied for modifying existing production strains and also pave the way for markerless whole genome modification studies in P. pastoris.
- 650 _2
- $a CRISPR-Cas systémy $7 D064113
- 650 _2
- $a oprava DNA spojením konců $7 D059766
- 650 _2
- $a genový knockout $x metody $7 D055786
- 650 _2
- $a genetické inženýrství $7 D005818
- 650 _2
- $a genetické markery $7 D005819
- 650 _2
- $a mutace INDEL $7 D054643
- 650 _2
- $a Pichia $x genetika $x růst a vývoj $7 D010843
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Fischer, Jasmin E $u Bisy e.U., Wetzawinkel, Hofstätten/Raab, Austria.
- 700 1_
- $a Raschmanová, Hana $u Department of Biotechnology, University of Chemistry and Technology Prague, Prague, Czech Republic.
- 700 1_
- $a Kniely, Claudia $u Institute of Molecular Biotechnology, Graz University of Technology, Graz, Austria.
- 700 1_
- $a Vogl, Thomas $u Institute of Molecular Biotechnology, Graz University of Technology, Graz, Austria.
- 700 1_
- $a Glieder, Anton $u Institute of Molecular Biotechnology, Graz University of Technology, Graz, Austria. Bisy e.U., Wetzawinkel, Hofstätten/Raab, Austria.
- 773 0_
- $w MED00002577 $t Journal of cellular biochemistry $x 1097-4644 $g Roč. 119, č. 4 (2018), s. 3183-3198
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/29091307 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190107 $b ABA008
- 991 __
- $a 20190122094329 $b ABA008
- 999 __
- $a ok $b bmc $g 1364008 $s 1039242
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 119 $c 4 $d 3183-3198 $e 20171226 $i 1097-4644 $m Journal of cellular biochemistry $n J Cell Biochem $x MED00002577
- LZP __
- $a Pubmed-20190107