Disruption of the MRP-L23 gene encoding the mitochondrial ribosomal protein L23 is lethal for Kluyveromyces lactis but not for Saccharomyces cerevisiae |
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Authors: | Gerald L. Murray Wei Guo Bao Hiroshi Fukuhara Xiao Ming Zuo G. Desmond Clark-Walker Xin Jie Chen |
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Affiliation: | (1) Molecular and Cellular Genetics Group, Research School of Biological Sciences, The Australian National University, Biology Place, RSBS Building, GPO Box 475, ACT 2601, Australia e-mail: chen@rsbs.anu.edu.au Tel.: +61-2-6249 4510; Fax: +61-2-6279 8294, AU;(2) Institut Curie, Section de Biologie, Centre Universitaire, 91405 Orsay, France, FR |
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Abstract: | The Kluyveromyces lactis nuclear gene, MRP-L23, encodes a polypeptide of 155 amino acids that shares 70% and 43% identity to the ribosomal proteins L23 and L13 of Saccharomyces cerevisiae and Escherichia coli. The deduced protein, designated KlL23, is a likely component of the large subunit of mitochondrial ribosomes as it can complement the respiratory deficient phenotype of a S. cerevisiae mrp-L23 mutant. As in S. cerevisiae, KlMRP-L23 is essential for respiratory growth of K. lactis because disruption of the gene in a “petite-positive” strain carrying a ρo-lethality suppressor atp mutation rendered cells unable to grow on a non-fermentable carbon source. However, in contrast to S. cerevisiae, disruption of MRP-L23 in wild type K. lactis is lethal. Meiotic segregants of K. lactis with a disrupted MRP-L23 allele form microcolonies with cell numbers varying from 32 to 300. These data clearly indicate an essential role of mitochondrial protein synthesis for viability of the petite-negative yeast K. lactis. Received: 2 September / 20 October 1999 |
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Keywords: | Kluyveromyces lactis Mitochondrial ribosomal protein ρ o-lethality L23 |
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