Literature DB >> 6330366

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

P P Müller, M K Reif, S Zonghou, C Sengstag, T L Mason, T D Fox.   

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.

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Year:  1984        PMID: 6330366     DOI: 10.1016/0022-2836(84)90178-5

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  58 in total

1.  Functional expression of a yeast mitochondrial intron-encoded protein requires RNA processing at a conserved dodecamer sequence at the 3' end of the gene.

Authors:  H Zhu; H Conrad-Webb; X S Liao; P S Perlman; R A Butow
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

2.  Saccharomyces cerevisiae positive regulatory gene PET111 encodes a mitochondrial protein that is translated from an mRNA with a long 5' leader.

Authors:  C A Strick; T D Fox
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

3.  The Saccharomyces cerevisiae ATP22 gene codes for the mitochondrial ATPase subunit 6-specific translation factor.

Authors:  Xiaomei Zeng; Audrey Hourset; Alexander Tzagoloff
Journal:  Genetics       Date:  2006-11-16       Impact factor: 4.562

4.  Product of Saccharomyces cerevisiae nuclear gene PET494 activates translation of a specific mitochondrial mRNA.

Authors:  M C Costanzo; T D Fox
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

5.  The MSS51 gene product is required for the translation of the COX1 mRNA in yeast mitochondria.

Authors:  E Decoster; M Simon; D Hatat; G Faye
Journal:  Mol Gen Genet       Date:  1990-10

6.  Effects of differential selection in the sexes on cytonuclear polymorphism and disequilibria.

Authors:  C S Babcock; M A Asmussen
Journal:  Genetics       Date:  1996-10       Impact factor: 4.562

7.  The PET54 gene of Saccharomyces cerevisiae: characterization of a nuclear gene encoding a mitochondrial translational activator and subcellular localization of its product.

Authors:  M C Costanzo; E C Seaver; T D Fox
Journal:  Genetics       Date:  1989-06       Impact factor: 4.562

8.  Antagonistic signals within the COX2 mRNA coding sequence control its translation in Saccharomyces cerevisiae mitochondria.

Authors:  Elizabeth H Williams; Thomas D Fox
Journal:  RNA       Date:  2003-04       Impact factor: 4.942

9.  PET111 acts in the 5'-leader of the Saccharomyces cerevisiae mitochondrial COX2 mRNA to promote its translation.

Authors:  J J Mulero; T D Fox
Journal:  Genetics       Date:  1993-03       Impact factor: 4.562

10.  Functional interactions among two yeast mitochondrial ribosomal proteins and an mRNA-specific translational activator.

Authors:  P Haffter; T W McMullin; T D Fox
Journal:  Genetics       Date:  1991-02       Impact factor: 4.562

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