Mitochondrial RNA Turnover in Metazoa

Author(s):  
Christoph Freyer ◽  
Paula Clemente ◽  
Anna Wredenberg
Genetics ◽  
1999 ◽  
Vol 151 (4) ◽  
pp. 1315-1325
Author(s):  
Wei Chen ◽  
Maria A Islas-Osuna ◽  
Carol L Dieckmann

Abstract The cytochrome b gene in Saccharomyces cerevisiae, COB, is encoded by the mitochondrial genome. Nuclear-encoded Cbp1 protein is required specifically for COB mRNA stabilization. Cbp1 interacts with a CCG element in a 64-nucleotide sequence in the 5′-untranslated region of COB mRNA. Mutation of any nucleotide in the CCG causes the same phenotype as cbp1 mutations, i.e., destabilization of both COB precursor and mature message. In this study, eleven nuclear suppressors of single-nucleotide mutations in CCG were isolated and characterized. One dominant suppressor is in CBP1, while the other 10 semidominant suppressors define five distinct linkage groups. One group of four mutations is in PET127, which is required for 5′ end processing of several mitochondrial mRNAs. Another mutation is linked to DSS1, which is a subunit of mitochondrial 3′ → 5′ exoribonuclease. A mutation linked to the SOC1 gene, previously defined by recessive mutations that suppress cbp1 ts alleles and stabilize many mitochondrial mRNAs, was also isolated. We hypothesize that the products of the two uncharacterized genes also affect mitochondrial RNA turnover.


2006 ◽  
Vol 17 (3) ◽  
pp. 1184-1193 ◽  
Author(s):  
Agata T. Rogowska ◽  
Olga Puchta ◽  
Anna M. Czarnecka ◽  
Aneta Kaniak ◽  
Piotr P. Stepien ◽  
...  

The Saccharomyces cerevisiae SUV3 gene encodes the helicase component of the mitochondrial degradosome (mtEXO), the principal 3′-to-5′ exoribonuclease of yeast mitochondria responsible for RNA turnover and surveillance. Inactivation of SUV3 (suv3Δ) causes multiple defects related to overaccumulation of aberrant transcripts and precursors, leading to a disruption of mitochondrial gene expression and loss of respiratory function. We isolated spontaneous suppressors that partially restore mitochondrial function in suv3Δ strains devoid of mitochondrial introns and found that they correspond to partial loss-of-function mutations in genes encoding the two subunits of the mitochondrial RNA polymerase (Rpo41p and Mtf1p) that severely reduce the transcription rate in mitochondria. These results show that reducing the transcription rate rescues defects in RNA turnover and demonstrates directly the vital importance of maintaining the balance between RNA synthesis and degradation.


Author(s):  
Ester A. Zylber ◽  
S. Perlman ◽  
Sheldon Penman

PLoS Genetics ◽  
2019 ◽  
Vol 15 (7) ◽  
pp. e1008240 ◽  
Author(s):  
Aleksandra Pajak ◽  
Isabelle Laine ◽  
Paula Clemente ◽  
Najla El-Fissi ◽  
Florian A. Schober ◽  
...  

2011 ◽  
Vol 39 (9) ◽  
pp. 3754-3770 ◽  
Author(s):  
Jesper Buchhave Poulsen ◽  
Kasper Røjkjær Andersen ◽  
Karina Hansen Kjær ◽  
Fiona Durand ◽  
Pierre Faou ◽  
...  

2009 ◽  
Vol 38 (1) ◽  
pp. 279-298 ◽  
Author(s):  
Roman J. Szczesny ◽  
Lukasz S. Borowski ◽  
Lien K. Brzezniak ◽  
Aleksandra Dmochowska ◽  
Kamil Gewartowski ◽  
...  

BIO-PROTOCOL ◽  
2015 ◽  
Vol 5 (20) ◽  
Author(s):  
Etienne Delannoy ◽  
And�ol Falcon de Longevialle ◽  
Catherine Francs-Small

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