KAR5 Encodes a Novel Pheromone-inducible Protein Required for Homotypic Nuclear Fusion
Open Access
- 1 December 1997
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 139 (5) , 1063-1076
- https://doi.org/10.1083/jcb.139.5.1063
Abstract
KAR5 is required for membrane fusion during karyogamy, the process of nuclear fusion during yeast mating. To investigate the molecular mechanism of nuclear fusion, we cloned and characterized the KAR5 gene and its product. KAR5 is a nonessential gene, and deletion mutations produce a bilateral defect in the homotypic fusion of yeast nuclei. KAR5 encodes a novel protein that shares similarity with a protein in Schizosaccharomyces pombe that may play a similar role in nuclear fusion. Kar5p is induced as part of the pheromone response pathway, suggesting that this protein uniquely plays a specific role during mating in nuclear membrane fusion. Kar5p is a membrane protein with its soluble domain entirely contained within the lumen of the endoplasmic reticulum. In pheromone-treated cells, Kar5p was localized to the vicinity of the spindle pole body, the initial site of fusion between haploid nuclei during karyogamy. We propose that Kar5p is required for the completion of nuclear membrane fusion and may play a role in the organization of the membrane fusion complex.Keywords
This publication has 64 references indexed in Scilit:
- A ten-minute DNA preparation from yeast efficiently releases autonomous plasmids for transformaion of Escherichia coliPublished by Elsevier ,2003
- Inner but Not Outer Membrane Leaflets Control the Transition from Glycosylphosphatidylinositol-anchored Influenza Hemagglutinin-induced Hemifusion to Full FusionThe Journal of cell biology, 1997
- Mechanisms of intracellular protein transportNature, 1994
- Implications of the SNARE hypothesis for intracellular membrane topology and dynamicsPublished by Elsevier ,1994
- Assembly and functions of the spindle pole body in budding yeastTrends in Genetics, 1993
- Components of the yeast spindle and spindle pole body.The Journal of cell biology, 1990
- Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferaseGene, 1988
- A simple method for displaying the hydropathic character of a proteinJournal of Molecular Biology, 1982
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970