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J E Hamer

Publications and source records attributed to J E Hamer.

38 records · Page 3Linked to original sources

Acropetal: a genetic locus required for conidiophore architecture and pathogenicity in the rice blast fungus.

Fungal spores are a primary means of dissemination and are the major sources of inoculum in pathogenic species. Sporulation in the rice blast fungus Magnaporthe grisea involves the production of three-celled conidia, borne sympodially on an aerial conidiophore. A disease cycle initiates when spores are dispersed and attach to the rice plant surface. Using insertional mutagenesis we have identified a major regulator of conidiophore morphogenesis in M. grisea. A null mutation in the acropetal (ACR1) locus causes a hypermorphic conidiation phenotype where indeterminate growth of the conidial tip cell results in the production of head-to-tail (acropetal) arrays of spores. acropetal mutants are nonpathogenic and fail to undergo infection-related morphogenesis. The ACR1 locus encodes a spore-specific transcript and acr1(-) mutants fail to turn off the expression of the hydrophobin encoding gene MPG1 in dormant spores. We propose that ACR1 is a stage-specific negative regulator of conidiation that is required to establish a sympodial pattern of spore formation. Interestingly a failure to establish the correct pattern of sporulation in M. grisea results in the production of spores that cannot progress through the disease cycle. Studies of Acropetal suggest that the diverse patterns of spore ontogeny in conidial fungi arose through alterations in major genes controlling spore-specific gene expression.

Amino Acid Sequence↗

Grasshopper, a long terminal repeat (LTR) retroelement in the phytopathogenic fungus Magnaporthe grisea.

The fungal phytopathogen Magnaporthe grisea parasitizes a wide variety of gramineous hosts. In the course of investigating the genetic relationship between pathogen genotype and host specificity we identified a retroelement that is present in some strains of M. grisea that infect finger millet and goosegrass (members of the plant genus Eleusine). The element, designated grasshopper (grh), is present in multiple copies and dispersed throughout the genome. DNA sequence analysis showed that grasshopper contains 198 base pair direct, long terminal repeats (LTRs) with features characteristic of retroviral and retrotransposon LTRs. Within the element we identified an open reading frame with sequences homologous to the reverse transcriptase, RNaseH, and integrase domains of retroelement pol genes. Comparison of the open reading frame with sequences from other retroelements showed that grh is related to the gypsy family of retrotransposons. Comparisons of the distribution of the grasshopper element with other dispersed repeated DNA sequences in M. grisea indicated that grasshopper was present in a broadly dispersed subgroup of Eleusine pathogens, suggesting that the element was acquired subsequent to the evolution of this host-specific form. We present arguments that the amplification of different retroelements within populations of M. grisea is a consequence of the clonal organization of the fungal populations.

Amino Acid Sequence↗