Abstract

We have determined the nucleotide sequence of the mim3-1 mitochondrial ribosomal suppressor, acting on ochre mitochondrial mutations and one frameshift mutation in Saccharomyces cerevisiae. The 15s rRNA suppressor gene contains a G633 to C transversion. Yeast mitochondrial G633 corresponds to G517 of the E.coli 15S rRNA, which is occupied by an invariant G in all known small rRNA sequences. Interestingly, this mutation has occurred at the same position as the known MSU1 mitochondrial suppressor which changes G633 to A. The suppressor mutation lies in a highly conserved region of the rRNA, known in E.coli as the 530-loop, interacting with the S4, S5 and S12 ribosomal proteins. We also show an interesting interaction between the mitochondrial mim3-1 and the nuclear nam3-1 suppressors, both of which have the same action spectrum on mitochondrial mutations: nam3-1 abolishes the suppressor effect when present with mim3-1 in the same haploid cell. We discuss these results in the light of the nature of Nam3, identified by 1 as the yeast mitochondrial translation release factor. A hypothetical mechanism of suppression by "ribosome shifting" is also discussed in view of the nature of mutations suppressed and not suppressed.

Highlights

  • Suppressors are divided into two wide groups: functional and informational

  • The situation is ideal in yeast mitochondria where the exceptional existence of only one copy of the small and large rRNA genes should allow the isolation of rRNA suppressors, if not lethal

  • Cloning and sequencing of various intronic trans-recessive mutations The mim3-1 suppressor was shown to be acting on various mitochondrial mutations located in different genes

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Summary

Introduction

Suppressors are divided into two wide groups: functional and informational The former ones are located in a second gene, the product of which interacts functionally with the mutated product of the first gene. The situation is ideal in yeast mitochondria where the exceptional existence of only one copy of the small and large rRNA genes should allow the isolation of rRNA suppressors, if not lethal. Such suppressors have been isolated already: mim by [5, 6] and MSU1 by [7]

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