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Lee-Parsons, C. W. T.

Publications and source records attributed to Lee-Parsons, C. W. T..

2 recordsLinked to original sources

CrJAMs are transcriptional repressors of the monoterpenoid indole alkaloid pathway in Catharanthus roseus

Catharanthus roseus produces monoterpenoid indole alkaloids (MIAs) in response to the defense hormone jasmonate (JA). In Arabidopsis, JA regulates defense processes through MYC2 and JA-Associated MYC2a-like transcription factors (JAMs). Here we characterize two previously identified C. roseus JAMs, CrJAM2 and CrJAM3, as regulators of MIA biosynthesis. Functional screens using viral-induced gene silencing and transient promoter activity assays showed that CrJAMs repress the MIA pathway; silencing both CrJAM2 and CrJAM3 increased expression of MIA pathway genes and MIA levels while their individual overexpression repressed promoter activity. To assess their activity broadly across MIA regulatory and biosynthetic genes, we generated C. roseus hairy root cultures either constitutively overexpressing individual CrJAMs or CRISPR-Cas9 creating mutations in multiple CrJAMs, and profiled their expression by RNA-Seq. CrJAM2 overexpression decreased expression of most MIA biosynthetic genes relative to the GUS control, while double mutant lines showed increased basal expression of these genes relative to non-targeting controls. Notably, methyl JA treatment perturbs this equilibrium, reversing these trends at 24 hrs in both CrJAM overexpression and mutant lines relative to basal conditions. In summary, CrJAMs broadly repress MIA regulatory and biosynthetic gene expression and together with CrJAZ and CrMYC2a regulates MIA biosynthesis.

plant biology↗

Addition of Multiple Introns to a Cas9 Gene Results in Dramatic Improvement in Efficiency for Generation of Gene Knockouts in Plants

The recent discovery of the mode of action of the CRISPR/Cas9 system has provided biologists with a useful tool for generating site-specific mutations in genes of interest. In plants, site-targeted mutations are usually obtained by stably transforming a Cas9 expression construct into the plant genome. The efficiency with which mutations are obtained in genes of interest can vary considerably depending on specific features of the constructs, including the source and nature of the promoters and terminators used for expression of the Cas9 gene and the guide RNA, and the sequence of the Cas9 nuclease itself. To optimize the efficiency with which mutations could be obtained in target genes in Arabidopsis thaliana with the Cas9 nuclease, we have investigated several features of its nucleotide and/or amino acid sequence, including the codon usage, the number of nuclear localization signals (NLS) and the presence or absence of introns. We found that the Cas9 gene codon usage had some effect on Cas9 activity and that two NLSs work better than one. However, the most important impact on the efficiency of the constructs was obtained by addition of 13 introns into the Cas9 coding sequence, which dramatically improved editing efficiencies of the constructs; none of the primary transformants obtained with a Cas9 lacking introns displayed a knockout mutant phenotype, whereas between 70% and 100% of primary transformants generated with intronized Cas9 displayed mutant phenotypes. The intronized Cas9 was also found to be effective in other plants such as Nicotiana benthamiana and Catharanthus roseus.

molecular biology↗