Ascofuranone suppresses invasion and F-actin cytoskeleton organization in cancer cells by inhibiting the mTOR complex 1 signaling pathway

2020 ◽  
Vol 43 (5) ◽  
pp. 793-805
Author(s):  
Yun-Jeong Jeong ◽  
Soon-Kyung Hwang ◽  
Junji Magae ◽  
Young-Chae Chang
Keyword(s):  
Actin Cytoskeleton ◽  
Cancer Cells ◽  
Signaling Pathway ◽  
Cytoskeleton Organization ◽  
Actin Cytoskeleton Organization ◽  
Mtor Complex 1

scholarly journals Pan1p, End3p, and Sla1p, Three Yeast Proteins Required for Normal Cortical Actin Cytoskeleton Organization, Associate with Each Other and Play Essential Roles in Cell Wall Morphogenesis

2000 ◽  
Vol 20 (1) ◽  
pp. 12-25 ◽  
Author(s):  
Hsin-Yao Tang ◽  
Jing Xu ◽  
Mingjie Cai
Keyword(s):  
Cell Wall ◽  
Actin Cytoskeleton ◽  
Normal Cell ◽  
Cell Cortex ◽  
Repeat Region ◽  
Cortical Actin ◽  
Cytoskeleton Organization ◽  
Eh Domain ◽  
Actin Cytoskeleton Organization ◽  
Cell Wall Morphogenesis

ABSTRACT The EH domain proteins Pan1p and End3p of budding yeast have been known to form a complex in vivo and play important roles in organization of the actin cytoskeleton and endocytosis. In this report, we describe new findings concerning the function of the Pan1p-End3p complex. First, we found that the Pan1p-End3p complex associates with Sla1p, another protein known to be required for the assembly of cortical actin structures. Sla1p interacts with the first long repeat region of Pan1p and the N-terminal EH domain of End3p, thus leaving the Pan1p-End3p interaction, which requires the second long repeat of Pan1p and the C-terminal repeat region of End3p, undisturbed. Second, Pan1p, End3p, and Sla1p are also required for normal cell wall morphogenesis. Each of the Pan1-4, sla1Δ, andend3Δ mutants displays the abnormal cell wall morphology previously reported for the act1-1 mutant. These cell wall defects are also exhibited by wild-type cells overproducing the C-terminal region of Sla1p that is responsible for interactions with Pan1p and End3p. These results indicate that the functions of Pan1p, End3p, and Sla1p in cell wall morphogenesis may depend on the formation of a heterotrimeric complex. Interestingly, the cell wall abnormalities exhibited by these cells are independent of the actin cytoskeleton organization on the cell cortex, as they manifest despite the presence of apparently normal cortical actin cytoskeleton. Examination of several act1 mutants also supports this conclusion. These observations suggest that the Pan1p-End3p-Sla1p complex is required not only for normal actin cytoskeleton organization but also for normal cell wall morphogenesis in yeast.

scholarly journals Golgi Body Motility in the Plant Cell Cortex Correlates with Actin Cytoskeleton Organization

2011 ◽  
Vol 52 (10) ◽  
pp. 1844-1855 ◽  
Author(s):  
Miriam Akkerman ◽  
Elysa J. R. Overdijk ◽  
Jan H. N. Schel ◽  
Anne Mie C. Emons ◽  
Tijs Ketelaar
Keyword(s):  
Actin Cytoskeleton ◽  
Plant Cell ◽  
Golgi Body ◽  
Cell Cortex ◽  
Cytoskeleton Organization ◽  
Actin Cytoskeleton Organization ◽  
Body Motility

The actin cytoskeleton is required to elaborate and maintain spatial patterning during trichome cell morphogenesis in Arabidopsis thaliana

Development ◽  
1999 ◽  
Vol 126 (24) ◽  
pp. 5559-5568 ◽  
Author(s):  
J. Mathur ◽  
P. Spielhofer ◽  
B. Kost ◽  
N. Chua
Keyword(s):  
Arabidopsis Thaliana ◽  
Actin Cytoskeleton ◽  
Spatial Patterning ◽  
Actin Microfilaments ◽  
Cell Morphogenesis ◽  
Actin Organization ◽  
Cytoskeleton Organization ◽  
Branch Formation ◽  
Actin Cytoskeleton Organization ◽  
Trichome Cell

Arabidopsis thaliana trichomes provide an attractive model system to dissect molecular processes involved in the generation of shape and form in single cell morphogenesis in plants. We have used transgenic Arabidopsis plants carrying a GFP-talin chimeric gene to analyze the role of the actin cytoskeleton in trichome cell morphogenesis. We found that during trichome cell development the actin microfilaments assumed an increasing degree of complexity from fine filaments to thick, longitudinally stretched cables. Disruption of the F-actin cytoskeleton by actin antagonists produced distorted but branched trichomes which phenocopied trichomes of mutants belonging to the ‘distorted’ class. Subsequent analysis of the actin cytoskeleton in trichomes of the distorted mutants, alien, crooked, distorted1, gnarled, klunker and wurm uncovered actin organization defects in each case. Treatments of wild-type seedlings with microtubule-interacting drugs elicited a radically different trichome phenotype characterized by isotropic growth and a severe inhibition of branch formation; these trichomes did not show defects in actin cytoskeleton organization. A normal actin cytoskeleton was also observed in trichomes of the zwichel mutant which have reduced branching. ZWICHEL, which was previously shown to encode a kinesin-like protein is thought to be involved in microtubule-linked processes. Based on our results we propose that microtubules establish the spatial patterning of trichome branches whilst actin microfilaments elaborate and maintain the overall trichome pattern during development.

ACTIN CYTOSKELETON ORGANIZATION IN OOCYTES AT VARIOUS STAGES OF DROSOPHILA MELANOGASTER OOGENESIS AFTER EXPOSURE IN A MICROGRAVITY SIMULATOR OVER THE COMPLETE GAMETOGENESIS CYCLE

2021 ◽  
Vol 55 (5) ◽  
pp. 59-63
Author(s):  
M.A. Usik ◽  
◽  
A.A. Sukonkina ◽  
I.V. Ogneva ◽  
◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Actin Cytoskeleton ◽  
Reproductive Potential ◽  
Immunohistochemical Analysis ◽  
Modeled Microgravity ◽  
Cytoskeleton Organization ◽  
Beta Actin ◽  
Actin Cytoskeleton Organization ◽  
Total Beta

The paper deals with the effects of modeled microgravity on actin cytoskeleton in oocytes at various stages of Drosophila melanogaster oogenesis over the complete gametogenesis cycle. Total actin content and F-actin singly was determined using immunohistochemical analysis. The results point to the growth of both total beta-actin and its polymer recognized by phalloidin. This finding can have key implications for evaluation of risks for the reproductive potential from the spaceflight factors.

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