Literature DB >> 8188749

Immunofluorescence localization of the unconventional myosin, Myo2p, and the putative kinesin-related protein, Smy1p, to the same regions of polarized growth in Saccharomyces cerevisiae.

S H Lillie1, S S Brown.   

Abstract

Myo2 protein (Myo2p), an unconventional myosin in the budding yeast Saccharomyces cerevisiae, has been implicated in polarized growth and secretion by studies of the temperature-sensitive myo2-66 mutant. Overexpression of Smy1p, which by sequence is a kinesin-related protein, can partially compensate for defects in the myo2 mutant (Lillie, S. H. and S. S. Brown, 1992. Nature (Lond.). 356:358-361). We have now immunolocalized Smy1p and Myo2p. Both are concentrated in regions of active growth, as caps at incipient bud sites and on small buds, at the mother-bud neck just before cell separation, and in mating cells as caps on shmoo tips and at the fusion bridge of zygotes. Double labeling of cells with either Myo2p or Smy1p antibody plus phalloidin was used to compare the localization of Smy1p and Myo2p to actin, and by extrapolation, to each other. These studies confirmed that Myo2p and Smy1p colocalize, and are concentrated in the same general regions of the cell as actin spots. However, neither colocalizes with actin. We noted a correlation in the behavior of Myo2p, Smy1p, and actin, but not microtubules, under a number of circumstances. In cdc4 and cdc11 mutants, which produce multiple buds, Myo2p and Smy1p caps were found only in the subset of buds that had accumulations of actin. Mutations in actin or secretory genes perturb actin, Smy1p and Myo2p localization. The rearrangements of Myo2p and Smy1p correlate temporally with those of actin spots during the cell cycle, and upon temperature and osmotic shift. In contrast, microtubules are not grossly affected by these perturbations. Although wild-type Myo2p localization does not require Smy1p, Myo2p staining is brighter when SMY1 is overexpressed. The myo2 mutant, when shifted to restrictive temperature, shows a permanent loss in Myo2p localization and actin polarization, both of which can be restored by SMY1 overexpression. However, the lethality of MYO2 deletion is not overcome by SMY1 overexpression. We noted that the myo2 mutant can recover from osmotic shift (unlike actin mutants; Novick, P., and D. Botstein. 1985. Cell. 40:405-416). We have also determined that the myo2-66 allele encodes a Lys instead of a Glu at position 511, which lies at an actin-binding face in the motor domain.

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Year:  1994        PMID: 8188749      PMCID: PMC2120074          DOI: 10.1083/jcb.125.4.825

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  42 in total

1.  Immunofluorescence localization of the Saccharomyces cerevisiae CDC12 gene product to the vicinity of the 10-nm filaments in the mother-bud neck.

Authors:  B K Haarer; J R Pringle
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

2.  Subcellular localization of Cdc42p, a Saccharomyces cerevisiae GTP-binding protein involved in the control of cell polarity.

Authors:  M Ziman; D Preuss; J Mulholland; J M O'Brien; D Botstein; D I Johnson
Journal:  Mol Biol Cell       Date:  1993-12       Impact factor: 4.138

3.  Effect of cell cycle position on thermotolerance in Saccharomyces cerevisiae.

Authors:  J Plesset; J R Ludwig; B S Cox; C S McLaughlin
Journal:  J Bacteriol       Date:  1987-02       Impact factor: 3.490

4.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

5.  Phenotypic analysis of temperature-sensitive yeast actin mutants.

Authors:  P Novick; D Botstein
Journal:  Cell       Date:  1985-02       Impact factor: 41.582

6.  A method for quantifying F-actin in chemotactic peptide activated neutrophils: study of the effect of tBOC peptide.

Authors:  T H Howard; C O Oresajo
Journal:  Cell Motil       Date:  1985

7.  Easy identification of cDNA clones.

Authors:  U Rüther; B Müller-Hill
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

8.  Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae.

Authors:  A E Adams; J R Pringle
Journal:  J Cell Biol       Date:  1984-03       Impact factor: 10.539

9.  Structural rearrangements of tubulin and actin during the cell cycle of the yeast Saccharomyces.

Authors:  J V Kilmartin; A E Adams
Journal:  J Cell Biol       Date:  1984-03       Impact factor: 10.539

10.  Diverse effects of beta-tubulin mutations on microtubule formation and function.

Authors:  T C Huffaker; J H Thomas; D Botstein
Journal:  J Cell Biol       Date:  1988-06       Impact factor: 10.539

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  138 in total

1.  Generation of an isogenic collection of yeast actin mutants and identification of three interrelated phenotypes.

Authors:  J Whitacre; D Davis; K Toenjes; S Brower; A Adams
Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

2.  Orphan kinesin NOD lacks motile properties but does possess a microtubule-stimulated ATPase activity.

Authors:  H J Matthies; R J Baskin; R S Hawley
Journal:  Mol Biol Cell       Date:  2001-12       Impact factor: 4.138

3.  Diverse protective roles of the actin cytoskeleton during oxidative stress.

Authors:  Michelle E Farah; Vladimir Sirotkin; Brian Haarer; David Kakhniashvili; David C Amberg
Journal:  Cytoskeleton (Hoboken)       Date:  2011-06-10

4.  Identification of two type V myosins in fission yeast, one of which functions in polarized cell growth and moves rapidly in the cell.

Authors:  F Motegi; R Arai; I Mabuchi
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

5.  Motor protein Myo5p is required to maintain the regulatory circuit controlling WOR1 expression in Candida albicans.

Authors:  Nadezda Kachurina; Bernard Turcotte; Malcolm Whiteway
Journal:  Eukaryot Cell       Date:  2012-03-09

6.  Two distinct myosin light chain structures are induced by specific variations within the bound IQ motifs-functional implications.

Authors:  Mohammed Terrak; Guanming Wu; Walter F Stafford; Renne C Lu; Roberto Dominguez
Journal:  EMBO J       Date:  2003-02-03       Impact factor: 11.598

7.  Signal-mediated depolymerization of actin in pollen during the self-incompatibility response.

Authors:  Benjamin N Snowman; David R Kovar; Galina Shevchenko; Vernonica E Franklin-Tong; Christopher J Staiger
Journal:  Plant Cell       Date:  2002-10       Impact factor: 11.277

8.  Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast.

Authors:  David Pruyne; Lina Gao; Erfei Bi; Anthony Bretscher
Journal:  Mol Biol Cell       Date:  2004-09-15       Impact factor: 4.138

Review 9.  Morphogenesis and the cell cycle.

Authors:  Audrey S Howell; Daniel J Lew
Journal:  Genetics       Date:  2012-01       Impact factor: 4.562

10.  Kif26b, a kinesin family gene, regulates adhesion of the embryonic kidney mesenchyme.

Authors:  Yukako Uchiyama; Masaji Sakaguchi; Takeshi Terabayashi; Toshiaki Inenaga; Shuji Inoue; Chiyoko Kobayashi; Naoko Oshima; Hiroshi Kiyonari; Naomi Nakagata; Yuya Sato; Kiyotoshi Sekiguchi; Hiroaki Miki; Eiichi Araki; Sayoko Fujimura; Satomi S Tanaka; Ryuichi Nishinakamura
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-03       Impact factor: 11.205

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