AN IN-VITRO TRANSCRIPTION ASSAY FOR YEAST MITOCHONDRIA USING ORGANELLAR LYSATES

The nuclear gene NUC1 encodes the major mitochondrial (mt) ribonucleas e in the yeast Saccharomyces cerevisiae. We describe an in vitro mt tr anscription assay system based on lysates of purified mitochondria fro m a petite (rho(-), mt deletion mutant) yeast strain in which NUC1 has been insertionally inactivated. Control in vitro run-on transcription assays using intact mitochondria demonstrate that the rate of incorpo ration of labeled precursor into mt RNA is identical in organelles fro m the nuc1 rho(-) mutant and its otherwise isochromosomal NUC1 parent strain. Brij-35 lysates of mitochondria from the nuc1 strain incorpora te precursor into mt RNA at nearly the same rate as do intact organell es hom that strain, while similar mt lysates from NUC1 cells show no s uch incorporation. Other control studies show that mt lysates from the nucl strain retain functional mt cAMP-dependent protein kinase and ot her critical activities. When the cloned template DNA encoding the yea st mt 21S rRNA gene, which is not retained in the nuc1 rho(-) strain, is added to mt lysates from that strain, transcripts are produced from the template under standard assay conditions. (C) 1996 Academic Press , Inc