Abstract

Gradients are used in a number of biological systems to transmit spatial information over a range of distances. The best studied are morphogen gradients where information is transmitted over many cell lengths. Smaller mitotic gradients reflect the need to organize several distinct events along the length of the mitotic spindle. The intracellular gradients that characterize mitosis are emerging as important regulatory paradigms. Intracellular gradients utilize intrinsic auto-regulatory feedback loops and diffusion to establish stable regions of activity within the mitotic cytosol. We review three recently described intracellular mitotic gradients. The Ran GTP gradient with its elaborate cascade of nuclear transport receptors and cargoes is the best characterized, yet the dynamics underlying the robust gradient of Ran-GTP have received little attention. Gradients of phosphorylation have been observed on Aurora B kinase substrates both before and after anaphase onset. In both instances the phosphorylation gradient appears to result from a soluble gradient of Aurora B kinase activity. Regulatory properties that support gradient formation are highlighted. Intracellular activity gradients that regulate localized mitotic events bare several hallmarks of self-organizing biologic systems that designate spatial information during pattern formation. Intracellular pattern formation represents a new paradigm in mitotic regulation.

Highlights

  • Spatial regulation during mitosis makes possible the equitable distribution of genetic material among daughter cells

  • Recent observations suggest that cells utilize intracellular gradients as the basis for the spatial regulation of mitotic events [1,2,3,4,5,6,7]

  • Intracellular gradients of phosphorylated stathmin [1], Ran-GTP [2], and most recently Aurora B kinase activity [3] act as spatial organizers by eliciting the discretely localized patterns of spindle, chromosome and cell membrane dynamics required for cell division [3,17,18]

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Summary

Introduction

Spatial regulation during mitosis makes possible the equitable distribution of genetic material among daughter cells. Intracellular gradients of phosphorylated stathmin [1], Ran-GTP [2], and most recently Aurora B kinase activity [3] act as spatial organizers by eliciting the discretely localized patterns of spindle, chromosome and cell membrane dynamics required for cell division [3,17,18]. These results are consistent with earlier data demonstrating that production of the RanGDP-RCC1 ternary complex is coupled to chromatin binding [55] This mechanism of Ran-GDP dependant targeting of RCC1 illustrates how catalytic production of an activator can reinforce the geographic localization of a gradient’s origin, underscoring the self-organizing nature of intracellular mitotic gradients as engines of positional information. This property, taken together with demonstrations of the self-organizing nature of the signal directing cytokinesis and its dependence on Aurora B activity, support the notion that the gradient of Aurora B activity might be the midzone signal responsible for directing the position of the cytokinetic furrow

Conclusion
24. Turing AM
26. Murray JD
34. Lewis J
41. Carlier MF
68. Uhlmann F
74. Glotzer M
Findings
79. Bringmann H
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