z-logo
open-access-imgOpen Access
Size Scaling of Microtubule Assemblies in EarlyXenopusEmbryos
Author(s) -
Timothy J. Mitchison,
Keisuke Ishihara,
Phuong Nguyen,
Martin Wühr
Publication year - 2015
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a019182
Subject(s) - biology , advanced spaceborne thermal emission and reflection radiometer , xenopus , mitosis , interphase , spindle apparatus , microbiology and biotechnology , cleavage (geology) , microtubule , blastomere , zygote , cytokinesis , cell division , embryo , microtubule organizing center , biophysics , cell , centrosome , cell cycle , genetics , embryogenesis , physics , gene , paleontology , satellite , astronomy , fracture (geology)
The first 12 cleavage divisions in Xenopus embryos provide a natural experiment in size scaling, as cell radius decreases ∼16-fold with little change in biochemistry. Analyzing both natural cleavage and egg extract partitioned into droplets revealed that mitotic spindle size scales with cell size, with an upper limit in very large cells. We discuss spindle-size scaling in the small- and large-cell regimes with a focus on the "limiting-component" hypotheses. Zygotes and early blastomeres show a scaling mismatch between spindle and cell size. This problem is solved, we argue, by interphase asters that act to position the spindle and transport chromosomes to the center of daughter cells. These tasks are executed by the spindle in smaller cells. We end by discussing possible mechanisms that limit mitotic aster size and promote interphase aster growth to cell-spanning dimensions.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom