2009
DOI: 10.1016/j.jbiotec.2008.10.007
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Gene targeting in a nonhomologous end joining deficient Hypocrea jecorina

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Cited by 130 publications
(119 citation statements)
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“…Deletion of the lxr4 Gene in T. reesei-A T. reesei ⌬tku70 strain was used as the parental strain for transformation (14,15). The cassette for deletion of the lxr4 gene (GenBank TM accession number BK008566) contained 937 bp of the promoter region, 1162 bp of the terminator region, and a fragment containing the pyr4 encoding orotidine-5Ј-phosphate decarboxylase.…”
Section: Methodsmentioning
confidence: 99%
“…Deletion of the lxr4 Gene in T. reesei-A T. reesei ⌬tku70 strain was used as the parental strain for transformation (14,15). The cassette for deletion of the lxr4 gene (GenBank TM accession number BK008566) contained 937 bp of the promoter region, 1162 bp of the terminator region, and a fragment containing the pyr4 encoding orotidine-5Ј-phosphate decarboxylase.…”
Section: Methodsmentioning
confidence: 99%
“…NHEJ repair has evolved as the predominant pathway in filamentous fungi, as in other superior eukaryotes, such as plants and mammals (106). In T. reesei as well as in other filamentous fungi, some components of the NHEJ pathway (mus53/lig4; TR_58509, TA_83609, and TV_180472 and ku70 homologs) have been the target of deletion in order to increase the proportion of homologous recombination events upon transformation for targeted gene replacement experiments (107)(108)(109). Homologs of all genes involved in NHEJ are present in the genomes of the Trichoderma species analyzed here (see Table S1 in the supplemental material).…”
Section: Dna Repairmentioning
confidence: 99%
“…Recent advances in method development have resulted in high-throughput generation of knockout/gene replacement strains by more efficient strategies, increasing the efficiency of homologous recombination and allowing sequential gene deletions. While these strategies have so far been applied to T. reesei QM9414-derived strains (Hartl & Seiboth, 2005;Guangtao et al, 2009) and the wild-type QM6a (Steiger et al, 2011), they could similarly be applied to the RUT-C30 strain. In addition, alternative strategies such as gene knock-down by mRNA silencing (reviewed by Nakayashiki et al, 2005) could be employed for partial or condition-specific suppression of gene expression, particularly when gene deletion could be detrimental or even lethal.…”
Section: Rut-c30 As a Host For Heterologous Protein Productionmentioning
confidence: 99%