The Arabidopsis thaliana Kinesin-5 AtKRP125b Is a Processive, Microtubule-Sliding Motor Protein with Putative Plant-Specific Functions

• Published in: International journal of molecular sciences 2021-10, Vol.22 (21), p.11361
• Main Authors: Strauß, Tobias, Schattner, Saskia, Hoth, Stefan, Walter, Wilhelm J
• Format: Article
• Language: English
• Subjects: Antibodies; Arabidopsis - metabolism; Arabidopsis Proteins - metabolism; Arabidopsis thaliana; Cell division; Confocal microscopy; Cotyledons; Crosslinking; Cytoplasm; Dyneins - metabolism; Epidermis; Genes; Interphase; Kinesin; Kinesins - genetics; Kinesins - metabolism; Microtubules; Microtubules - metabolism; Mitosis; Molecular Motor Proteins - metabolism; Molecular motors; Myosins - metabolism; Nuclei (cytology); Proteins; Protoplasts; Roots; Spindle Apparatus - metabolism; Spindles; Vascular tissue; Velocity; Vertebrates
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms222111361

The formation and maintenance of the mitotic spindle during cell division requires several microtubule-interacting motor proteins. Members of the kinesin-5 family play an essential role in the bipolar organization of the spindle. These highly conserved, homotetrameric proteins cross-link anti-parallel microtubules and slide them apart to elongate the spindle during the equal separation of chromosomes. Whereas vertebrate kinesin-5 proteins are well studied, knowledge about the biochemical properties and the function of plant kinesin-5 proteins is still limited. Here, we characterized the properties of AtKRP125b, one of four kinesin-5 proteins in . In in vitro motility assays, AtKRP125b displayed the archetypal characteristics of a kinesin-5 protein, a low velocity of about 20 nm·s , and a plus end-directed, processive movement. Moreover, AtKRP125b was able to cross-link microtubules and to slide them apart, as required for developing and maintaining the mitotic spindle. In line with such a function, GFP-AtKRP125b fusion proteins were predominantly detected in the nucleus when expressed in leaf protoplasts or epidermis cells and analyzed by confocal microscopy. However, we also detected GFP signals in the cytoplasm, suggesting additional functions. By generating and analyzing promoter-reporter lines, we showed that the promoter was active in the vascular tissue of roots, lateral roots, cotyledons, and true leaves. Remarkably, we could not detect promoter activity in meristematic tissues. Taken together, our biochemical data support a role of AtKRP125b in mitosis, but it may also have additional functions outside the nucleus and during interphase.