spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by TORRE, D. L.
Right arrow Articles by GIMENEZ-MARTIN, G.
Right arrow Search for Related Content
PubMed
Right arrow Articles by TORRE, D. L.
Right arrow Articles by GIMENEZ-MARTIN, G.

Journal of Cell Science, Vol 94, 259-265, Copyright © 1989 by Company of Biologists

Submitted on April 28, 1989
Accepted on June 9, 1989

Stringency at four regions of the plant cell cycle where proteins regulating its progression are synthesized

DE LA TORRE 1, A. GONZALEZ-FERNADEZ 1, and G. GIMENEZ-MARTIN 1

1 Centro de Investigaciones Biológicas, CSIC. Velázquez, 144. 28006-Madrid, Spain

Different responses were detected when inhibiting protein synthesis (by 1µgml-1 anisomycin) for similar times (3 h) in each of the four regions of the plant cell cycle where synthesis of specific proteins seems to control further cycle progression. Synchronous cells, labelled as binucleate by 1-h, 5 mM-caffeine treatment, were used for this study in Allium cepa L. root meristems proliferating under steady-state kinetics.

In the experimental conditions used, G1 lasts 8 h in the synchronous control populations. G1 houses two such regions. The first region is located in early G1. Inhibition of protein synthesis in this region produced 8.2 h of delay in reaching the S period. Moreover, the treatment halved the proliferative fraction of the population, behaving as a restriction area where cells should be rendered competent to go on cycling by newly synthesized proteins. The second region, located in late G1 (before the 6th hour of the cycle), produced, when inhibiting protein synthesis in the population, a delay of 2.4 h (shorter than the treatment) in reaching the S period and no decrease of its proliferative fraction.

A similar inhibition of protein synthesis in the third region mapped in early G2 (before the 20th hour of the cell cycle) produced 4.4 h of delay in reaching mitosis and a 20 % decrease in the proliferative fraction. Finally, there is a fourth region in early prophase (before the 25th hour of the cell cycle) where all the cells seemed to abandon the cycle during inhibition of protein synthesis.

Note:
This article is dedicated to Dr F. A. L. Clowes, Oxford, on the occasion of his retirement.

Key words: G1, G2, prophase, cycle regulation, transition points, control points, protein synthesis, excess delays

Submitted on April 28, 1989
Accepted on June 9, 1989




This article has been cited by other articles:


Home page
J. Cell Sci.Home page
A. Gonzalez-Fernandez, J. Sans, P. Aller, and C. De La Torre
The involvement of discrete genome regions in post-mitotic chromosome decondensation and in G1 timing in Allium cepa L. meristematic cells
J. Cell Sci., December 1, 1992; 103(4): 1047 - 1051.
[Abstract] [PDF]




© The Company of Biologists Ltd 1989