scholarly journals Myosin II is an Active Stress Sensor at the Core of a Cell Division Control System

2010 ◽  
Vol 98 (3) ◽  
pp. 161a-162a
Author(s):  
Yee Seir Kee ◽  
Richard Firtel ◽  
Pablo Iglesias ◽  
Douglas Robinson
1971 ◽  
Vol 17 (1) ◽  
pp. 119-122 ◽  
Author(s):  
R. J. L. Paulton

Synchronously dividing cultures of Bacillus subtilis were obtained by harvesting cells from the stationary phase and reincubating them in fresh medium. It was discovered that the first division period was not necessarily synchronous, but when the first synchronous division occurred it involved a reduction in septation. These findings suggested that cell synthesis was directed to more than the forthcoming division, and that synchronization involved a subsequent division and a change in the cell division control mechanism.


1993 ◽  
Vol 90 (24) ◽  
pp. 12030-12034 ◽  
Author(s):  
R. G. Faragher ◽  
I. R. Kill ◽  
J. A. Hunter ◽  
F. M. Pope ◽  
C. Tannock ◽  
...  
Keyword(s):  

2014 ◽  
Vol 19 (5) ◽  
pp. 405-418 ◽  
Author(s):  
Tomohiro Shimada ◽  
Kaori Shimada ◽  
Makoto Matsui ◽  
Yuichi Kitai ◽  
Jun Igarashi ◽  
...  

2012 ◽  
Vol 490-495 ◽  
pp. 594-597
Author(s):  
Cheng Qun Li ◽  
Liang Gao

This paper introduces a new type of automatic steel bundling machine for bundling process, which includes a pneumatic action process, mainly do some researches on the pneumatic control system. The system chooses PLC as the core control component, puts forward the hardware of control system and control flow. Eventually we have been designed the control program.


1989 ◽  
Vol 139 (2) ◽  
pp. 269-274 ◽  
Author(s):  
Heideh Fattaey ◽  
Terry C. Johnson ◽  
Hsin-Hwei Chou

2010 ◽  
Vol 2010 ◽  
pp. 1-13 ◽  
Author(s):  
Fei Xue ◽  
Deanna M. Janzen ◽  
David A. Knecht

Numerous F-actin containing structures are involved in regulating protrusion of membrane at the leading edge of motile cells. We have investigated the structure and dynamics of filopodia as they relate to events at the leading edge and the function of the trailing actin networks. We have found that although filopodia contain parallel bundles of actin, they contain a surprisingly nonuniform spatial and temporal distribution of actin binding proteins. Along the length of the actin filaments in a single filopodium, the most distal portion contains primarily T-plastin, while the proximal portion is primarily bound byα-actinin and coronin. Some filopodia are stationary, but lateral filopodia move with respect to the leading edge. They appear to form a mechanical link between the actin polymerization network at the front of the cell and the myosin motor activity in the cell body. The direction of lateral filopodial movement is associated with the direction of cell migration. When lateral filopodia initiate from and move toward only one side of a cell, the cell will turn opposite to the direction of filopodial flow. Therefore, this filopodia-myosin II system allows actin polymerization driven protrusion forces and myosin II mediated contractile force to be mechanically coordinated.


1991 ◽  
Vol 11 (10) ◽  
pp. 5301-5311
Author(s):  
J A Brown ◽  
S G Holmes ◽  
M M Smith

The chromatin structures of two well-characterized autonomously replicating sequence (ARS) elements were examined at their chromosomal sites during the cell division cycle in Saccharomyces cerevisiae. The H4 ARS is located near one of the duplicate nonallelic histone H4 genes, while ARS1 is present near the TRP1 gene. Cells blocked in G1 either by alpha-factor arrest or by nitrogen starvation had two DNase I-hypersensitive sites of about equal intensity in the ARS element. This pattern of DNase I-hypersensitive sites was altered in synchronous cultures allowed to proceed into S phase. In addition to a general increase in DNase I sensitivity around the core consensus sequence, the DNase I-hypersensitive site closest to the core consensus became more nuclease sensitive than the distal site. This change in chromatin structure was restricted to the ARS region and depended on replication since cdc7 cells blocked near the time of replication initiation did not undergo the transition. Subsequent release of arrested cdc7 cells restored entry into S phase and was accompanied by the characteristic change in ARS chromatin structure.


2017 ◽  
Vol 95 (3) ◽  
Author(s):  
Jacopo Grilli ◽  
Matteo Osella ◽  
Andrew S. Kennard ◽  
Marco Cosentino Lagomarsino

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