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Utah State University

Series

1996

Articles 1 - 2 of 2

Full-Text Articles in Biology

Mutations In Trans-Acting Factors Affecting Mrna Decapping In Saccharomyces Cereviciae, Lianna K. Etchberger, C. A. Stevens, A. Stevens, R. Parker Jan 1996

Mutations In Trans-Acting Factors Affecting Mrna Decapping In Saccharomyces Cereviciae, Lianna K. Etchberger, C. A. Stevens, A. Stevens, R. Parker

Biology Faculty Publications

The decay of several yeast mRNAs occurs by a mechanism in which deadenylation precedes decapping and subsequent 5'-to-3' exonucleolytic decay. In order to identify gene products required for this process of mRNA turnover, we screened a library of temperature-sensitive strains for mutants with altered mRNA degradation. We identified seven mutations in four genes that inhibited mRNA turnover. Two mutations were alleles of the XRN1 5'-to-3' exoribonuclease known to degrade mRNAs following decapping. One mutation defined a new gene, termed DCP1, which in subsequent work was demonstrated to encode a decapping enzyme or a necessary component of a decapping complex. The …


Fate Of Biological Control Introductions: Monitoring An Australian Fungal Pathogen Of Grasshoppers In North America, Michael J. Bidochka, Scott R. A. Walsh, Mark E. Ramos, Raymond J. St. Leger, Julie Cl Silver, Donald W. Roberts Jan 1996

Fate Of Biological Control Introductions: Monitoring An Australian Fungal Pathogen Of Grasshoppers In North America, Michael J. Bidochka, Scott R. A. Walsh, Mark E. Ramos, Raymond J. St. Leger, Julie Cl Silver, Donald W. Roberts

Biology Faculty Publications

In North America there are two generally recognized pathotypes (pathotypes 1 and 2) of the fungus Entomophaga grylli which show host-preferential infection of grasshopper subfamilies. Pathotype 3, discovered in Austra- lia,hasabroadergrasshopperhostrangeandwasconsidered to be a good biocontrol agent. Between 1989 and 1991 patho- type3wasintroducedattwofieldsitesinNorthDakota.Since resting spores are morphologically indistinguishable among pathotypes, we used pathotype-specific DNA probes to con- firm pathotype identification in E. grylli-infected grasshop- pers collected at the release sites in 1992, 1993, and 1994. In 1992, up to 23% of E. grylli-infected grasshoppers of the subfamilies Melanoplinae, Oedipodinae, and Gomphocerinae were infected by pathotype 3,with no infections >1 km …