2017
DOI: 10.21775/cimb.021.041
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Genome Editing with Engineered Nucleases in Economically Important Animals and Plants: State of the Art in the Research Pipeline

Abstract: After induced mutagenesis and transgenesis,

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Cited by 10 publications
(9 citation statements)
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References 94 publications
(218 reference statements)
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“…Our literature search also covered publications of nGM applications that are near commercialization or already commercialized in some countries, such as a herbicide-resistant oilseed rape variety developed by ODM (Gocal et al, 2015). As seen in Sovova et al (2017) information on patents did not add significant information in terms of application and the potential for commercialization. We are thus confident that the sources we have considered sufficiently serve the purpose of this work.…”
Section: Literature Survey To Identify Applications Of Ngms With Relementioning
confidence: 94%
“…Our literature search also covered publications of nGM applications that are near commercialization or already commercialized in some countries, such as a herbicide-resistant oilseed rape variety developed by ODM (Gocal et al, 2015). As seen in Sovova et al (2017) information on patents did not add significant information in terms of application and the potential for commercialization. We are thus confident that the sources we have considered sufficiently serve the purpose of this work.…”
Section: Literature Survey To Identify Applications Of Ngms With Relementioning
confidence: 94%
“…The advantage of meganucleases is their small size, making them appropriate to a majority of delivery methods [16]. However, the DNA-binding domain cannot be separated from the catalytic domain challenging the construction of MN [4]. MN have been applied successfully for genome editing in plants such as Arabidopsis [17], maize [18] and cotton [19].…”
Section: Meganucleasesmentioning
confidence: 99%
“…ZFN are generated by fusing two independent protein domains. A zinc-finger protein, which comprises up to six zinc-finger domains each able to identify a nucleotide triplet of a specific DNA sequence, is fused with a synthetic endonuclease domain (most frequently FokI) [4,9,29]. Since the nuclease is active as a dimer, two zinc-finger nucleases are necessary in close proximity to target and cut a sequence in the genome.…”
Section: Zinc-finger Nucleasesmentioning
confidence: 99%
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“…The features of clustered regularly interspaced short palindromic repeats (CRISPR) were discovered serendipitously in the genomes of various bacteria and archaea during molecular biology studies ( Ishino et al, 1987 ; Mojica et al, 1993 ). The system was originally used as an adaptive immune defense system by bacteria against the invasion of foreign nucleic acids, such as viruses and plasmids ( Ishino et al, 1987 ; Sovova et al, 2017 ; Albitar et al, 2018 ). The immune process is divided into three stages: 1) adaptation: the invading nucleotide fragments are first captured by the host organism, and subsequently, a Cas integrase-derived nucleic acid sequence is inserted into the CRISPR array; 2) biogenesis: the CRISPR array is transcribed into a pre-crRNA (pre-crRNA) containing a spacer and a portion of the repeat, which is subsequently cleaved in the repeat to induce the generation of mature guide crRNA (gRNA); and 3) interference: mature crRNA-Cas complexes recognize specific sites on target nucleic acids through complementary base pairing, triggering Cas enzymes to catalyze the cleavage of effector complexes of invading nucleotides ( Debin Zhang et al, 2020 ; Makarova et al, 2020 ).…”
Section: Introductionmentioning
confidence: 99%