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Genetic Analysis of Growth Inhibition of Yeast Cells Caused by Expression ofAspergillus oryzaeRNase T1
Author(s) -
Gen aka,
T. Ishikawa,
Tin-tin LIU,
Harushi Nakajima,
Katsuhiko Kitamoto
Publication year - 2000
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.64.2152
Subject(s) - rnase p , aspergillus oryzae , complementary dna , biology , yeast , rnase mrp , microbiology and biotechnology , plasmid , expression vector , cytosol , growth inhibition , cell fractionation , golgi apparatus , biochemistry , enzyme , cell growth , gene , endoplasmic reticulum , rna , recombinant dna
Even though most fungal hydrolytic enzymes have been successfully secreted in S. cerevisiae cells by expression of corresponding cDNA, overexpression of A. oryzae RNase T1 causes severe growth inhibition in yeast. We observed that yeast strains carrying RNase T1 cDNA under control of the GAL1 promoter with a single-copy vector were able to grow on galactose medium while those with a multi-copy vector were not. It was found that overexpression of three mutated versions of RNase T1 with low enzymatic activity did not affect the growth. We also observed that expression of RNase T1 without a signal sequence severely inhibited growth of the transformant even on the single-copy plasmid. Subcellular fractionation showed that overexpressed myc-tagged RNase T1 was localized in the membrane fraction. In the yeast secretory pathway, while the mutants defective in translocation into the ER, ER-Golgi trafficking and vacuole formation had severe growth inhibition during expression of RNase T1 from the single-copy plasmid. These results suggest that a mislocalization of active RNase T1 in cytosol by overflow from the secretory apparatus has toxic effects on the host cells.

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