Bulk Cytoplasmic Actin and Its Functions in Meiosis and Mitosis

Slides:



Advertisements
Similar presentations
Cell Division (Mitosis)
Advertisements

Mechanisms and Molecules of the Mitotic Spindle
Carly I. Dix, Jordan W. Raff  Current Biology 
Organelle Transport: A Park-and-Ride System for Melanosomes
Volume 16, Issue 2, Pages (January 2006)
Plant Growth: Jogging the Cell Cycle with JAG
Mitosis: New Roles for Myosin-X and Actin at the Spindle
Evidence for an Upper Limit to Mitotic Spindle Length
Nuclear Envelope Breakdown: Actin’ Quick to Tear Down the Wall
Bacterial Size: Can’t Escape the Long Arm of the Law
Sensory-Motor Integration: More Variability Reduces Individuality
Nanosecond-scale kinetics of nematocyst discharge
Visual Development: Learning Not to See
Cargo Transport: Two Motors Are Sometimes Better Than One
Cell Division: Experiments and Modelling Unite to Resolve the Middle
Microtubule Flux: What Is It Good for?
Meiosis: Organizing Microtubule Organizers
Spindle Pole Regulation by a Discrete Eg5-Interacting Domain in TPX2
Volume 25, Issue 24, Pages R1156-R1158 (December 2015)
Volume 20, Issue 22, Pages (November 2010)
Xenopus Current Biology
Spindle Positioning: Actin Mediates Pushing and Pulling
And the Dead Shall Rise: Actin and Myosin Return to the Spindle
Number of Nuclear Divisions in the Drosophila Blastoderm Controlled by Onset of Zygotic Transcription  Hung-wei Sung, Saskia Spangenberg, Nina Vogt, Jörg.
Volume 18, Issue 19, Pages (October 2008)
Asymmetric Positioning and Organization of the Meiotic Spindle of Mouse Oocytes Requires CDC42 Function  Jie Na, Magdalena Zernicka-Goetz  Current Biology 
Live Imaging of Endogenous RNA Reveals a Diffusion and Entrapment Mechanism for nanos mRNA Localization in Drosophila  Kevin M. Forrest, Elizabeth R.
Zhang-Yi Liang, Mark Andrew Hallen, Sharyn Anne Endow  Current Biology 
Spindle Pole Regulation by a Discrete Eg5-Interacting Domain in TPX2
Guillaume Halet, John Carroll  Developmental Cell 
Naoyuki Fuse, Kanako Hisata, Alisa L. Katzen, Fumio Matsuzaki 
Volume 17, Issue 6, Pages (March 2007)
Cryptosporidium Current Biology
Kai Yuan, Antony W. Shermoen, Patrick H. O’Farrell  Current Biology 
The Timing of Midzone Stabilization during Cytokinesis Depends on Myosin II Activity and an Interaction between INCENP and Actin  Jennifer Landino, Ryoma.
A Comparative Analysis of Spindle Morphometrics across Metazoans
Sophie Louvet-Vallée, Stéphanie Vinot, Bernard Maro  Current Biology 
Functional Comparison of H1 Histones in Xenopus Reveals Isoform-Specific Regulation by Cdk1 and RanGTP  Benjamin S. Freedman, Rebecca Heald  Current Biology 
P granules Current Biology
Visual Development: Learning Not to See
Meiosis: Checking Chromosomes Pair up Properly
Centrosome Size: Scaling Without Measuring
S. Chodagam, A. Royou, W. Whitfield, R. Karess, J.W. Raff 
Justin Crest, Kirsten Concha-Moore, William Sullivan  Current Biology 
Regulation of MBK-2/Dyrk Kinase by Dynamic Cortical Anchoring during the Oocyte-to- Zygote Transition  Michael L. Stitzel, Ken Chih-Chien Cheng, Geraldine.
Volume 19, Issue 21, Pages (November 2009)
A New Model for Asymmetric Spindle Positioning in Mouse Oocytes
Volume 16, Issue 6, Pages (March 2006)
Victoria Stevenson, Andrew Hudson, Lynn Cooley, William E Theurkauf 
Anaphase B Precedes Anaphase A in the Mouse Egg
Volume 18, Issue 15, Pages R641-R645 (August 2008)
HURP Is Part of a Ran-Dependent Complex Involved in Spindle Formation
Mi Hye Song, L. Aravind, Thomas Müller-Reichert, Kevin F. O'Connell 
Volume 20, Issue 22, Pages (November 2010)
Anna Marie Sokac, Eric Wieschaus  Developmental Cell 
The Origin of Centrosomes in Parthenogenetic Hymenopteran Insects
Transcriptional and Developmental Functions of the H3
Plant Development: Lessons from Getting It Twisted
Julie C Canman, David B Hoffman, E.D Salmon  Current Biology 
Intracellular Transport: How Do Motors Work Together?
Anisotropic Diffusion of Macromolecules in the Contiguous Nucleocytoplasmic Fluid during Eukaryotic Cell Division  Nisha Pawar, Claudia Donth, Matthias.
Closed Mitosis: A Timely Move before Separation
Volume 21, Issue 11, Pages (June 2011)
Volume 18, Issue 18, Pages (September 2008)
Mitotic Spindle Assembly and Chromosome Segregation
Volume 15, Issue 19, Pages (October 2005)
Volume 18, Issue 5, Pages R198-R202 (March 2008)
Meiotic sex chromosome inactivation
Volume 21, Issue 7, Pages (April 2011)
The Drosophila Microtubule-Associated Protein Mini Spindles Is Required for Cytoplasmic Microtubules in Oogenesis  Woongjoon Moon, Tulle Hazelrigg  Current.
Presentation transcript:

Bulk Cytoplasmic Actin and Its Functions in Meiosis and Mitosis Christine M. Field, Péter Lénárt  Current Biology  Volume 21, Issue 19, Pages R825-R830 (October 2011) DOI: 10.1016/j.cub.2011.07.043 Copyright © 2011 Elsevier Ltd Terms and Conditions

Figure 1 Known cellular functions of bulk cytoplasmic actin. (A) In meiotic starfish oocytes, chromosomes (red dots) scattered in the large nuclear volume are transported to the cell cortex by a contractile F-actin mesh (green). The F-actin meshwork contracts homogeneously; directionality is provided by anchoring to the cell cortex. Chromosomes are larger than the mesh size of the network and thus captured and transported by the network by passive sieving. (B) In the meiotic mouse oocyte, the spindle with chromosomes (red) needs to be transported to the cell cortex to ensure the asymmetry of division. Here, the F-actin mesh (green) serves as a substrate that provides tracks for transport driven by myosin motors or actin polymerization. (C) Microtubule-driven cytoplasmic streaming is prevented by an F-actin mesh (green) during oogenesis in Drosophila. A simple explanation could be that the F-actin mesh acts passively as a sieve to prevent the motion of cellular components (e.g. vesicles). Current Biology 2011 21, R825-R830DOI: (10.1016/j.cub.2011.07.043) Copyright © 2011 Elsevier Ltd Terms and Conditions

Figure 2 M-phase microtubules are relatively short in large cells and are insufficient to connect to the cell cortex or capture chromosomes scattered in the cytoplasm. (A) A representative somatic cell (HeLa) in metaphase (image courtesy of Mayumi Isokane). (B) The first meiotic spindle in a mouse oocyte (image courtesy of Melina Schuh). (C) The first cleavage division of a Xenopus egg (image courtesy of Martin Wühr). For all images, cells were fixed and stained with an anti-tubulin antibody (yellow) and for DNA (red). The red dashed circle indicates the cell outline. The numbers at the bottom indicate the cell diameter (‘Cell') and the length of the long spindle axis (‘Spindle'). Current Biology 2011 21, R825-R830DOI: (10.1016/j.cub.2011.07.043) Copyright © 2011 Elsevier Ltd Terms and Conditions

Figure 3 Bulk cytoplasmic actin is regulated by the cell cycle. (A) Xenopus egg extracts prepared without cytochalasin contract if in M phase, but spread out in interphase. (B) In early sand dollar embryos, the amount of bulk cytoplasmic actin polymer is dramatically increased in M phase. F-actin is concentrated at the cortex in all stages. Embryos were fixed at different stages of the cell cycle and stained with phalloidin (red) and anti-tubulin antibody (green). Images are courtesy of George von Dassow and Victoria Foe. Current Biology 2011 21, R825-R830DOI: (10.1016/j.cub.2011.07.043) Copyright © 2011 Elsevier Ltd Terms and Conditions