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TPX2-LIKE PROTEIN3 Is the Primary Activator of α-Aurora Kinases and Is Essential for Embryogenesis
J. Boruc, X. Deng, E. Mylle, N. Besbrugge, M. Van Durme, D. Demidov, ED. Tomaštíková, TC. Tan, M. Vandorpe, D. Eeckhout, T. Beeckman, MK. Nowack, G. De Jaeger, H. Lin, B. Liu, D. Van Damme,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S.
NLK
Free Medical Journals
od 1926 do Před 1 rokem
Open Access Digital Library
od 1926-01-01
PubMed
31097675
DOI
10.1104/pp.18.01515
Knihovny.cz E-zdroje
- MeSH
- aktivace enzymů genetika MeSH
- Arabidopsis embryologie genetika metabolismus MeSH
- geneticky modifikované rostliny MeSH
- konfokální mikroskopie MeSH
- protein-serin-threoninkinasy genetika metabolismus MeSH
- proteiny asociované s mikrotubuly genetika metabolismus MeSH
- proteiny buněčného cyklu genetika metabolismus MeSH
- proteiny huseníčku genetika metabolismus MeSH
- proteomika metody MeSH
- regulace genové exprese u rostlin MeSH
- sekvence aminokyselin MeSH
- sekvenční homologie aminokyselin MeSH
- semena rostlinná embryologie genetika metabolismus MeSH
- vazba proteinů MeSH
- vývojová regulace genové exprese MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
Aurora kinases are key regulators of mitosis. Multicellular eukaryotes generally possess two functionally diverged types of Aurora kinases. In plants, including Arabidopsis (Arabidopsis thaliana), these are termed α- and β-Auroras. As the functional specification of Aurora kinases is determined by their specific interaction partners, we initiated interactomics analyses using both Arabidopsis α-Aurora kinases (AUR1 and AUR2). Proteomics results revealed that TPX2-LIKE PROTEINS2 and 3 (TPXL2/3) prominently associated with α-Auroras, as did the conserved TPX2 to a lower degree. Like TPX2, TPXL2 and TPXL3 strongly activated the AUR1 kinase but exhibited cell-cycle-dependent localization differences on microtubule arrays. The separate functions of TPX2 and TPXL2/3 were also suggested by their different influences on AUR1 localization upon ectopic expressions. Furthermore, genetic analyses showed that TPXL3, but not TPX2 and TPXL2, acts nonredundantly to enable proper embryo development. In contrast to vertebrates, plants have an expanded TPX2 family and these family members have both redundant and unique functions. Moreover, as neither TPXL2 nor TPXL3 contains the C-terminal Kinesin-5 binding domain present in the canonical TPX2, the targeting and activity of this kinesin must be organized differently in plants.
Citace poskytuje Crossref.org
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