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Mitochondrial import and localization of CLK-1 in Caenorhabditis elegans

Several classes of genes determine the lifespan of the nematode Caenorhabditis elegans. Our laboratory is particularly interested in the clk class of genes that is composed of clk-1, clk-2, clk-3 , and gro-1. Mutations in these genes have been shown to extend lifespan and to deregulate several developmental and behavioural processes such as pharyngeal pumping and defecation cycle length. / clk-1 encodes a 187 amino acid mitochondrial protein that is composed of two homologous TRC domains (TRC for T&barbelow;andemly R&barbelow;epeated in C&barbelow;LK-1). Interestingly, the yeast homologue of clk-1, COQ7, has been implicated in ubiquinone biosynthesis. clk-1 (e2519) lesion is a point mutation that changes a conserved amino acid (E148K) in the second TRC domain. A structural model proposed that clk-1 is a di-iron carboxylate protein. We found that mutations in the di-iron binding center abolish CLK-1 activity and modify the subcellular distribution of CLK-1 in clk-1( qm30) null mutants.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:QMM.33853
Date January 2001
CreatorsUbach, Antonio.
ContributorsHekimi, Siegfried (advisor)
PublisherMcGill University
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Formatapplication/pdf
CoverageMaster of Science (Department of Biology.)
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
Relationalephsysno: 001872096, proquestno: MQ78970, Theses scanned by UMI/ProQuest.

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