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PMID: 7348598 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Tubulin content and synthesis in differentiating Drosophila cells in culture.

Cell motility ·Vol. 1 ·No. 1 ·1980-00-00 ·Pages 113-29

Berger EM, Sloboda RD, Ireland RC

Abstract

Drosophila Kc cells exposed to physiological doses of the moulting hormone, beta-ecdysone, elongate, become motile, and subsequently aggregate. This pattern of morphogenesis was found to require the assembly of a microtubular cytoskeleton. Tubulin content was significantly increased in hormone-treated cells when compared to controls, as measured by a 3H-colchicine-binding assay. However, determinations of rates of tubulin synthesis and breakdown revealed no difference between control and hormone-treated cells for either parameter. When tubulin content was assayed by methods that do not depend on colchicine-binding activity, no difference between hormone-treated and control cells was observed. These results are discussed in terms of a model in which beta-ecdysone affects the distribution of tubulin in "assembly-active" and "assembly-inactive" pools.

MeSH Terms
Actins/metabolism Animals Cell Differentiation Cells, Cultured Colchicine/metabolism Drosophila Ecdysterone/pharmacology Microtubule-Associated Proteins Microtubules/metabolism Proteins/metabolism Tubulin/metabolism
Chemicals
Actins Microtubule-Associated Proteins Proteins Tubulin Ecdysterone Colchicine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Berger E M
Sloboda R D
Ireland R C
Article Info
Journal
Cell motility
Abbr.
Cell Motil
ISSN
0271-6585
Published
1980-00-00
Pages
113-29
Language
English
Region
United States
NLM ID
8207421
Subset
IM
Grants
NIGMS NIH HHS · GM-22866 · United States
NIGMS NIH HHS · GM-25061 · United States
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