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Cell Growth and Development

Characterization of a Ustilago maydisGene Specifically Induced during the Biotrophic Phase: Evidence for Negative as Well as Positive Regulation

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Pages 329-339 | Received 27 Jul 1999, Accepted 04 Oct 1999, Published online: 28 Mar 2023
 

Abstract

The phytopathogenic basidiomycete Ustilago maydisrequires its host plant, maize, for completion of its sexual cycle. To investigate the molecular events during infection, we used differential display to identify plant-induced U. maydis genes. We describe the U. maydis gene mig1 (for “maize-induced gene”), which is not expressed during yeast-like growth of the fungus, is weakly expressed during filamentous growth in axenic culture, but is extensively upregulated during plant infection.mig1 encodes a small, highly charged protein of unknown function which contains a functional N-terminal secretion sequence and is not essential for pathogenic development. Adjacent tomig1 is a second gene (mdu1) related tomig1, which appears to result from a gene duplication.mig1 gene expression during the infection cycle was assessed by fusing the promoter to eGFP. Expression of mig1 was absent in hyphae growing on the leaf surface but was detected after penetration and remained high during subsequent proliferation of the fungus until teliospore formation. Successive deletions as well as certain internal deletions in the mig1promoter conferred elevated levels of reporter gene expression during growth in axenic culture, indicative of negative regulation. During fungal growth in planta, sequence elements between positions −148 and −519 in the mig1 promoter were specifically required for high levels of induction, illustrating additional positive control. We discuss the potential applications of mig1 for the identification of inducing compounds and the respective regulatory genes.

ACKNOWLEDGMENTS

We thank Nicole Euer and Sebastian Kolb for constructing plasmids and Christine Kerschbamer for providing technical assistance.

This work was supported by the Leibniz program of the DFG and by SFB369.

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