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Toward Understanding the Sexual Development in the Homothallic Ascomycete Gibberella zeae

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154

Symposia

S19-4

Toward Understanding the Sexual Development

in the Homothallic Ascomycete Gibberella zeae

Sung-Hwan Yun1 * and Yin-Won Lee2

1Department of Medical Biotechnology, Soonchunhyang University, Asan 336-745

2Department of Agricultural Biotechnology, Seoul National University, Seoul 151-921

Gibberella zeae (anamorph Fusarium graminearum) is a filamentous homothallic ascomycete with

ubiquitous geographic distribution. This fungus causes serious diseases in cereal crops, such as corn, wheat, barley, and rice [1]. These diseases not only reduce grain yield but also threaten to human and animal health due to contamination of the diseased grain with mycotoxins. Sexual spores (ascospores) of G. zeae, which are produced within sexual fruit-bodies called perithecia formed on plant debris, are forcibly discharged from the perithecia and can infect plant spikes via the anther during anthesis in the next spring [2]. Therefore, ascospore production caused by sexual development has been suggested to play important roles in completing the cycle of the plant diseases caused by G. zeae. Here, we focus on the G. zeae sexual developmental processes genetically controlled by the mating-type locus (MAT), a single master regulator for mating. G. zeae carries two alternate idiomorphs (alleles, MAT1-1 and MAT1-2) in a single nucleus, only each of which is present in heterothallic species [3, 4]. To massively isolate and characterize genes involved in sexual development from the G. zeae genome, we have employed several functional genomics approaches. First, we have generated and characterized a collection of insertional mutants from a representative strain of G. zeae using the restriction enzyme-mediated integration (REMI) procedure. Second, we have determined the functions of more than 100 genes using a targeted gene deletion strategy. Those genes were selected based on sequence analyses of REMI mutation genes, their neighbors, and orthologs of previously identified fungal genes, and selected by a small-scale microarray or proteomics analysis using a MAT1-2-deleted strain [5, 6]. In this talk, functional characterization of the genes mainly involved in pheromone- or G-protein signaling, mating-type-mediated sexual development pathway, or their related secondary metabolism in G. zeae were presented [7].

References

[1] M McMullen, R Jones and D Gallenberg. Plant Dis 81, 1340 (1997). [2] F Trail, H Xu, R Loranger and D Gadoury. Mycologia 92, 130 (2002).

[3] SH Yun, T Arie, I Kaneko, OC Yoder and BG Turgeon. Fungal Genet Biol 31, 7 (2000). [4] J Lee, T Lee, YW Lee, SH Yun and BG Turgeon. Mol Microbiol 50, 145 (2003). [5] SH Lee, S Lee, D Choi, YW Lee and SH Yun. Fungal Genet Biol 43,295 (2006). [6] SH Lee, YK Kim, SH Yun and YW Lee. Curr Genet 53, 175 (2008).

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