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Novel class of nuclear genes involved in both mRNA splicing and protein synthesis in Saccharomyces cerevisiae mitochondria
Authors:Edna Ben Asher   Olga Groudinsky   Geneviève Dujardin   Nicola Altamura   Michèle Kermorgant  Piotr P. Slonimski
Affiliation:(1) Centre de Génétique Moléculaire du C.N.R.S., Laboratoire propre associé à l'Université P. et M. Curie, F-91198 Gif-sur-Yvette Cedex, France;(2) Present address: Department of Genetics, The Weizmann Institute, 76100 Rehovot, Israél;(3) Present address: Centro di Studio sui Mitocondri e Metabolismo Energetico, CNR, c/o Dipartimento di Biochimica e Biologia Molecolare, Università di Bari, Via Amendola, 165/A, I-70126 Bari, Italy
Abstract:
Summary We have cloned three distinct nuclear genes, NAM1, NAM7, and NAM8, which alleviate mitochondrial intron mutations of the cytochrome b and COXI (subunit I of cytochrome oxidase) genes when present on multicopy plasmids. These nuclear genes show no sequence homology to each other and are localized on different chromosomes: NAM1 on chromosome IV, NAM7 on chromosome XIII and NAM8 on chromosome VIII. Sequence analysis of the NAM1 gene shows that it encodes a protein of 440 amino acids with a typical presequence that would target the protein to the mitochondrial matrix. Inactivation of the NAM1 gene by gene transplacement leads to a dramatic reduction of the overall synthesis of mitochondrial protein, and a complete absence of the COXI protein which is the result of a specific block in COXI pre-mRNA splicing. The possible mechanisms by which the NAM1 gene product may function are discussed.
Keywords:Yeast  Nuclear genes  Mitochondrial translation  Mitochondrial splicing  Suppression
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