4.4 Article

Conditional promoters for analysis of essential genes in Zymoseptoria tritici

期刊

FUNGAL GENETICS AND BIOLOGY
卷 79, 期 -, 页码 166-173

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.fgb.2015.03.024

关键词

Inducible-repressible promoter; Fungal wheat pathogen; Septoria tritici blotch; Mycosphaerella graminicola

资金

  1. Biotechnology & Biological Sciences Research Council [BB/I020667/1]
  2. Biotechnology and Biological Sciences Research Council [BB/I020667/1, BB/I025956/1] Funding Source: researchfish
  3. BBSRC [BB/I025956/1, BB/I020667/1] Funding Source: UKRI

向作者/读者索取更多资源

Development of new fungicides, needed for sustainable control of fungal plant pathogens, requires identification of novel anti-fungal targets. Essential fungal-specific proteins are good candidates, but due to their importance, gene deletion mutants are not viable. Consequently, their cellular role often remains elusive. This hindrance can be overcome by the use of conditional mutants, where expression is controlled by an inducible/repressible promoter. Here, we introduce 5 inducible/repressible promoter systems to study essential genes in the wheat pathogen Zymoseptoria tritici. We fused the gene for enhanced green-fluorescent protein (egfp) to the promoter region of Z. tritici nitrate reductase (Pnar1; induced by nitrogen and repressed by ammonium), 1,4-beta-endoxylanase A (Pex1A; induced by xylose and repressed by maltodextrin), L-arabinofuranosidase B (PlaraB; induced by arabinose and repressed by glucose), galactose-1-phosphate uridylyltransferase 7 (Pgal7; induced by galactose and repressed by glucose) and isocitrate lyase (Picl1; induced by sodium acetate and repressed by glucose). This was followed by quantitative analysis of cytoplasmic reporter fluorescence under induced and repressed conditions. We show that Pnar1,PlaraB and Pex1A drive very little or no egfp expression when repressed, but induce moderate protein production when induced. In contrast, Pgal7 and Picl1 show considerable egfp expression when repressed, and were strongly induced in the presence of their inducers. Normalising the expression levels of all promoters to that of the alpha-tubulin promoter Ptub2 revealed that PlaraB was the weakest promoter (similar to 20% of Ptub2), whereas Picl1 strongly expressed the reporter (similar to 250% of Ptub2). The use of these tools promises a better understanding of essential genes, which will help developing novel control strategies that protect wheat from Z. tritici. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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