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PMID: 6330366 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

A nuclear mutation that post-transcriptionally blocks accumulation of a yeast mitochondrial gene product can be suppressed by a mitochondrial gene rearrangement.

Journal of molecular biology ·Vol. 175 ·No. 4 ·1984-06-05 ·Pages 431-52

Müller PP, Reif MK, Zonghou S, Sengstag C, Mason TL, Fox TD

Abstract

The nuclear amber mutation, pet494-1, specifically blocks the accumulation of the product of the mitochondrial gene oxi2, cytochrome oxidase subunit III. The pet494-1 mutation does not prevent transcription of the mitochondrial gene since RNA--gel blot hybridizations showed that mutant cells contain normal amounts of an oxi2 transcript, indistinguishable in size from wild-type. A mitochondrial mutation that partially suppresses the nuclear mutation was isolated. The "mitochondrial revertant" behaved as though it contained two different mitochondrial DNAs: one rho+, the other rho-. The suppressor mutation is carried on the rho- mitochondrial DNA and is apparently the result of a gene fusion between oxi2 and another mitochondrial gene, oxi3. This gene rearrangement replaced the normal 5'-non-translated sequence of oxi2 with a portion of the open reading frame of the second intron of oxi3. Novel transcripts of the rearranged gene, containing oxi3 sequences upstream from oxi2 were detected in the mitochondrial revertant. The strain accumulated an electrophoretically variant form of cytochrome oxidase subunit III, probably translated from a new initiation codon. The data are consistent with models in which the PET494 protein acts within the mitochondria to specifically promote the translation of the oxi2 messenger RNA.

MeSH Terms
DNA, Mitochondrial/genetics Electron Transport Complex IV/biosynthesis,genetics Genes, Fungal Mitochondria Models, Genetic Mutation Nucleic Acid Hybridization Protein Biosynthesis RNA, Messenger/genetics Saccharomyces cerevisiae/enzymology,genetics Suppression, Genetic Transcription, Genetic
Chemicals
DNA, Mitochondrial RNA, Messenger Electron Transport Complex IV
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Müller P P
Reif M K
Zonghou S
Sengstag C
Mason T L
Fox T D
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1984-06-05
Pages
431-52
Language
English
Region
England
NLM ID
2985088R
Subset
IM
Grants
NIGMS NIH HHS · GM29362 · United States
NICHD NIH HHS · HD00515 · United States
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