Abstract
Higher plants represent a large group of eukaryotes where centrosomes are absent. The functions of γ-tubulin small complexes (γ-TuSCs) and γ-tubulin ring complexes (γ-TuRCs) in metazoans and fungi in microtubule nucleation are well established and the majority of components found in the complexes are present in plants. However, plant microtubules are also nucleated in a γ-tubulin-dependent but γ-TuRC-independent manner. There is growing evidence that γ-tubulin is a microtubule nucleator without being complexed in γ-TuRC. Fibrillar arrays of γ-tubulin were demonstrated in plant and animal cells and the ability of γ-tubulin to assemble into linear oligomers/polymers was confirmed in vitro for both native and recombinant γ-tubulin. The functions of γ-tubulin as a template for microtubule nucleation or in promoting spontaneous nucleation is outlined. Higher plants represent an excellent model for studies on the role of γ-tubulin in nucleation due to their acentrosomal nature and high abundancy and conservation of γ-tubulin including its intrinsic ability to assemble filaments. The defining scaffolding or sequestration functions of plant γ-tubulin in microtubule organization or in nuclear processes will help our understanding of its cellular roles in eukaryotes.
Highlights
Microtubules are dynamic tubular polymers composed of α,β-tubulin heterodimers with diverse functions in cell division, cell transport processes, organelle positioning and many other cellular functions
It is known that γ-tubulin is essential for the nucleation of phragmoplast microtubules [12,13]. γ-Tubulin associates with microtubules in cells with an impaired function of γ-tubulin ring complexes (γ-TuRCs) and nucleation of specific microtubular arrays of plants may be promoted by γ-tubulin which is not complexed with GCPs [57]
Arabidopsis and human γ-tubulin are conserved on the sequence and structural levels
Summary
Microtubules are dynamic tubular polymers composed of α,β-tubulin heterodimers with diverse functions in cell division, cell transport processes, organelle positioning and many other cellular functions. The spatio–temporal control of microtubule formation is a prerequisite for the assembly of specific microtubular arrays and for the proper functioning of the microtubular cytoskeleton. Microtubules are nucleated and organized from microtubule-organizing centers (MTOCs) such as centrosomes in metazoans or spindle pole bodies in fungi. Centrosome equivalents are still present in ancient land plants like ferns, mosses and liverworts [1], while higher plants represent a large group of eukaryotes that lack centrosomes in all somatic and gametic cells
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