Novel additions to the CRISPR/Cas tool box beyond SpCas9. Advances in Chemical Biology
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F19%3A00503190" target="_blank" >RIV/68378050:_____/19:00503190 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Novel additions to the CRISPR/Cas tool box beyond SpCas9. Advances in Chemical Biology
Popis výsledku v původním jazyce
Clustered regularly interspaced short palindromic repeats (CRISPRs) are found in archaea and many bacteria were they play a role in adaptive immunity against invasion of foreign genetic elements in the form of plasmids or bacteriophages. This bacterial defense machinery acts via specific degradation of the invading nucleic acid by nucleases. In this system, the invading genetic element is recognized by a complex of a short RNA molecule (the guide RNA) and a protein containing nuclease activity. In 2013, the CRISPR/Cas system has been repurposed and converted into a programmable tool for precision genome engineering. The first and most prominent member of the CRISPR/Cas systems employed as a programmable nuclease is Streptococcus pyogenes Cas9 (SpCas9) and it became the best studied and most widely used ribo-nuclease today in a broad range of applications. Despite the great success of Cas9, the search and harnessing of other, alternative orthologue CRISPR systems continued expanding our toolbox for genomic manipulations, transcriptional regulation or sequence specific detection of nucleic acids. Since these newly discovered CRISPR systems complement the functionality and provide interesting alternatives to SpCas9, with promising advantages regarding the size, specificity and additional features, we highlight the new additions to the CRISPR-toolbox in this mini-review.
Název v anglickém jazyce
Novel additions to the CRISPR/Cas tool box beyond SpCas9. Advances in Chemical Biology
Popis výsledku anglicky
Clustered regularly interspaced short palindromic repeats (CRISPRs) are found in archaea and many bacteria were they play a role in adaptive immunity against invasion of foreign genetic elements in the form of plasmids or bacteriophages. This bacterial defense machinery acts via specific degradation of the invading nucleic acid by nucleases. In this system, the invading genetic element is recognized by a complex of a short RNA molecule (the guide RNA) and a protein containing nuclease activity. In 2013, the CRISPR/Cas system has been repurposed and converted into a programmable tool for precision genome engineering. The first and most prominent member of the CRISPR/Cas systems employed as a programmable nuclease is Streptococcus pyogenes Cas9 (SpCas9) and it became the best studied and most widely used ribo-nuclease today in a broad range of applications. Despite the great success of Cas9, the search and harnessing of other, alternative orthologue CRISPR systems continued expanding our toolbox for genomic manipulations, transcriptional regulation or sequence specific detection of nucleic acids. Since these newly discovered CRISPR systems complement the functionality and provide interesting alternatives to SpCas9, with promising advantages regarding the size, specificity and additional features, we highlight the new additions to the CRISPR-toolbox in this mini-review.
Klasifikace
Druh
C - Kapitola v odborné knize
CEP obor
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OECD FORD obor
10608 - Biochemistry and molecular biology
Návaznosti výsledku
Projekt
<a href="/cs/project/LO1220" target="_blank" >LO1220: CZ-OPENSCREEN: Národní infrastruktura chemické biologie</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název knihy nebo sborníku
Advances in Chemical Biology
ISBN
978-80-88011-03-3
Počet stran výsledku
9
Strana od-do
104-113
Počet stran knihy
210
Název nakladatele
OPTIO CZ
Místo vydání
Praha
Kód UT WoS kapitoly
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