Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/112109
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dc.titleThe EH-domain-containing protein Pan1 is required for normal organization of the actin cytoskeleton in Saccharomyces cerevisiae
dc.contributor.authorTang, H.-Y.
dc.contributor.authorCai, M.
dc.date.accessioned2014-11-28T02:53:18Z
dc.date.available2014-11-28T02:53:18Z
dc.date.issued1996
dc.identifier.citationTang, H.-Y.,Cai, M. (1996). The EH-domain-containing protein Pan1 is required for normal organization of the actin cytoskeleton in Saccharomyces cerevisiae. Molecular and Cellular Biology 16 (9) : 4897-4914. ScholarBank@NUS Repository.
dc.identifier.issn02707306
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/112109
dc.description.abstractNormal cell growth and division in the yeast Saccharomyces cerevisiae involve dramatic and frequent changes in the organization of the actin cytoskeleton. Previous studies have suggested that the reorganization of the actin cytoskeleton in accordance with cell cycle progression is controlled, directly or indirectly, by the cyclin-dependent kinase Cdc28. Here we report that by isolating rapid-death mutants in the background of the Start- deficient cdc28-4 mutation, the essential yeast gene PAN1, previously thought to encode the yeast poly(A) nuclease, is identified as a new factor required for normal organization of the actin cytoskeleton. We show that at restrictive temperature, the pan1 mutant exhibited abnormal bud growth, failed to maintain a proper distribution of the actin cytoskeleton, was unable to reorganize actin the cytoskeleton during cell cycle, and was defective in cytokinesis. The mutant also displayed a random pattern of budding even at permissive temperature. Ectopic expression of PAN1 by the GAL promoter caused abnormal distribution of the actin cytoskeleton when a single-copy vector was used. Immunofluorescence staining revealed that the Paul protein colocalized with the cortical actin patches, suggesting that it may be a filamentous actin-binding protein. The Pant protein contains an EF- hand calcium-binding domain, a putative Src homology 3 (SH3)-binding domain, a region similar to the actin cytoskeleton assembly control protein Sla1, and two repeats of a newly identified protein motif known as the EH domain. These findings suggest that Pan1, recently recognized as not responsible for the poly(A) nuclease activity (A. B. Sachs and J. A. Deardorff, erratum, Cell 83:1059, 1995; R. Boeck, S. Tarun, Jr., M. Rieger, J. A. Deardorff, S. Muller-Auer, and A. B. Sachs, J. Biol. Chem. 271:432-438, 1996), plays an important role in the organization of the actin cytoskeleton in S. cerevisiae.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitleMolecular and Cellular Biology
dc.description.volume16
dc.description.issue9
dc.description.page4897-4914
dc.description.codenMCEBD
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Staff Publications

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