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Transcriptional profiling and functional analysis of heterokaryon incompatibility in Neurospora crassa reveals that reactive oxygen species, but not metacaspases, are associated with programmed cell death

Authors :
Elizabeth A. Hutchison
Chaoguang Tian
N. Louise Glass
Sarah K. Brown
Source :
Microbiology. 155:3957-3970
Publication Year :
2009
Publisher :
Microbiology Society, 2009.

Abstract

Heterokaryon incompatibility (HI) is a nonself recognition phenomenon occurring in filamentous fungi that is important for limiting resource plundering and restricting viral transfer between strains. Nonself recognition and HI occurs during hyphal fusion between strains that differ athetloci. If two strains undergo hyphal fusion, but differ in allelic specificity at ahetlocus, the fusion cell is compartmentalized and undergoes a rapid programmed cell death (PCD). Incompatible heterokaryons show a macroscopic phenotype of slow growth and diminished conidiation, and a microscopic phenotype of hyphal compartmentation and cell death. To understand processes associated with HI and PCD, we used whole-genome microarrays forNeurospora crassato assess transcriptional differences associated with induction of HI mediated by differences inhet-c pin-chaplotype. Our data show that HI is a dynamic and transcriptionally active process. The production of reactive oxygen species is implicated in the execution of HI and PCD inN. crassa, as are several genes involved in phosphatidylinositol and calcium signalling pathways. However, genes encoding mammalian homologues of caspases or apoptosis-inducing factor (AIF) are not required for HI or programmed cell death. These data indicate that PCD during HI occurs via a novel and possibly fungal-specific mechanism, making this pathway an attractive drug target for control of fungal infections.

Details

ISSN :
14652080 and 13500872
Volume :
155
Database :
OpenAIRE
Journal :
Microbiology
Accession number :
edsair.doi.dedup.....79d029b1bc63ec5a85519ea4e86c09c4
Full Text :
https://doi.org/10.1099/mic.0.032284-0