4.8 Article

Arabidopsis Fused kinase and the Kinesin-12 subfamily constitute a signalling module required for phragmoplast expansion

期刊

PLANT JOURNAL
卷 72, 期 2, 页码 308-319

出版社

WILEY
DOI: 10.1111/j.1365-313X.2012.05077.x

关键词

TWO-IN-ONE; Fused kinase; pollen mitosis I; cytokinesis; Kinesin-12 subfamily; phragmoplast expansion

资金

  1. UK Biotechnology and Biological Sciences Research Council (BBSRC) [BB/E001017/1, BB/I011269/1]
  2. National Research Foundation of Korea [2011-0011141]
  3. Rural Development Administration, Republic of Korea (Plant Molecular Breeding Center) [PJ008137]
  4. BBSRC [BB/E001017/1, BB/I011269/1] Funding Source: UKRI
  5. Biotechnology and Biological Sciences Research Council [BB/E001017/1, BB/I011269/1] Funding Source: researchfish
  6. National Research Foundation of Korea [2011-0011141] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The conserved Fused kinase plays vital but divergent roles in many organisms from Hedgehog signalling in Drosophila to polarization and chemotaxis in Dictyostelium. Previously we have shown that Arabidopsis Fused kinase termed TWO-IN-ONE (TIO) is essential for cytokinesis in both sporophytic and gametophytic cell types. Here using in vivo imaging of GFP-tagged microtubules in dividing microspores we show that TIO is required for expansion of the phragmoplast. We identify the phragmoplast-associated kinesins, PAKRP1/Kinesin-12A and PAKRP1L/Kinesin-12B, as TIO-interacting proteins and determine TIO-Kinesin-12 interaction domains and their requirement in male gametophytic cytokinesis. Our results support the role of TIO as a functional protein kinase that interacts with Kinesin-12 subfamily members mainly through the C-terminal ARM repeat domain, but with a contribution from the N-terminal kinase domain. The interaction of TIO with Kinesin proteins and the functional requirement of their interaction domains support the operation of a Fused kinase signalling module in phragmoplast expansion that depends upon conserved structural features in diverse Fused kinases.

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