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???displayArticle.abstract??? MELK has been implicated in a large variety of functions. Because its level is elevated in cancer tissues and it is involved in cell proliferation, MELK is considered as a potential therapeutic target for cancers. In a recent, study we have shown that MELK is involved in cytokinesis in early Xenopus laevis embryos. MELK dynamically accumulates at the cell cortex including a narrow band corresponding to the presumptive division furrow shortly before cytokinesis onset. MELK co-localizes and interacts with anillin an important regulator of cytokinesis. In addition, MELK overexpression interferes with accumulation at the cleavage furrow of activated Rho GTPase another crucial regulator of cytokinesis. Interestingly, our study also revealed that a transition implying a change in the direction of asymmetric furrow ingression occurs during early development. After this transition, MELK, as well as other proteins involved in cytokinesis, do not localize anymore as a band at the equatorial cortex but still localizes at the cell cortex. Our results indicate that cortical localization is an important feature of MELK in X. laevis embryos.
Figure 1. ME LK localization in epithelial cells of Xenopus gastrula embryos. (A) Indirect immunofluorescence with anti-MELK antibodies. Endogenous
MELK is detected at the cell cortex in interphase cell (arrowhead) and further accumulates at the cell cortex at the metaphase to anaphase transition
(m: metaphase, a: anaphase). The yellow line on the scheme at the bottom indicates the position of the confocal plane relative to the cell surface. DN A
(blue) which is situated more profoundly in the cells was merged with overlaying ME LK signal. (B and C) The mRNA coding for GFP tagged ME LK inactive
mutant (GFP-MELK K/R) which does not induce cytokinesis failure was microinjected in an embryo at the two cell stage and GFP-MELK K/R was
followed in a live gastrulaembryo. Two confocal planes taken at the same time are shown. GFP-MELK K/R is localized at the cell cortex of interphase
cells (i: interphase cell, arrowhead in b and c) and further accumulates at the cell cortex in cytokinetic cell (cyt). Note that the apical domain of the
cytokinetic cell is beginning its division whereas its baso-lateral membrane is already divided. * and ** indicate the two forming daughter cells to
facilitate analysis of the original figure and the related scheme at the bottom.
Audhya,
A complex containing the Sm protein CAR-1 and the RNA helicase CGH-1 is required for embryonic cytokinesis in Caenorhabditis elegans.
2005, Pubmed
Audhya,
A complex containing the Sm protein CAR-1 and the RNA helicase CGH-1 is required for embryonic cytokinesis in Caenorhabditis elegans.
2005,
Pubmed
Badouel,
Maternal embryonic leucine zipper kinase is stabilized in mitosis by phosphorylation and is partially degraded upon mitotic exit.
2010,
Pubmed
,
Xenbase
Badouel,
M-phase MELK activity is regulated by MPF and MAPK.
2006,
Pubmed
,
Xenbase
Bement,
A microtubule-dependent zone of active RhoA during cleavage plane specification.
2005,
Pubmed
,
Xenbase
Blot,
Cell cycle regulation of pEg3, a new Xenopus protein kinase of the KIN1/PAR-1/MARK family.
2002,
Pubmed
,
Xenbase
Chartrain,
Cell-cycle-dependent cortical localization of pEg3 protein kinase in Xenopus and human cells.
2006,
Pubmed
,
Xenbase
Cordes,
The C. elegans MELK ortholog PIG-1 regulates cell size asymmetry and daughter cell fate in asymmetric neuroblast divisions.
2006,
Pubmed
Daub,
Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.
2008,
Pubmed
Davezac,
Human pEg3 kinase associates with and phosphorylates CDC25B phosphatase: a potential role for pEg3 in cell cycle regulation.
2002,
Pubmed
,
Xenbase
Dephoure,
A quantitative atlas of mitotic phosphorylation.
2008,
Pubmed
Gray,
Maternal embryonic leucine zipper kinase/murine protein serine-threonine kinase 38 is a promising therapeutic target for multiple cancers.
2005,
Pubmed
Hebbard,
Maternal embryonic leucine zipper kinase is upregulated and required in mammary tumor-initiating cells in vivo.
2010,
Pubmed
Heyer,
New member of the Snf1/AMPK kinase family, Melk, is expressed in the mouse egg and preimplantation embryo.
1997,
Pubmed
Le Page,
A functional analysis of MELK in cell division reveals a transition in the mode of cytokinesis during Xenopus development.
2011,
Pubmed
,
Xenbase
Lin,
Involvement of maternal embryonic leucine zipper kinase (MELK) in mammary carcinogenesis through interaction with Bcl-G, a pro-apoptotic member of the Bcl-2 family.
2007,
Pubmed
Maddox,
Anillin and the septins promote asymmetric ingression of the cytokinetic furrow.
2007,
Pubmed
Marie,
Maternal embryonic leucine zipper kinase transcript abundance correlates with malignancy grade in human astrocytomas.
2008,
Pubmed
Mirey,
CDC25B phosphorylated by pEg3 localizes to the centrosome and the spindle poles at mitosis.
2005,
Pubmed
Nakano,
Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation.
2005,
Pubmed
Nakano,
Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells.
2008,
Pubmed
Paris,
Poly(A) metabolism and polysomal recruitment of maternal mRNAs during early Xenopus development.
1990,
Pubmed
,
Xenbase
Pickard,
Dysregulated expression of Fau and MELK is associated with poor prognosis in breast cancer.
2009,
Pubmed
Prodon,
Dual mechanism controls asymmetric spindle position in ascidian germ cell precursors.
2010,
Pubmed
Reinsch,
Orientation of spindle axis and distribution of plasma membrane proteins during cell division in polarized MDCKII cells.
1994,
Pubmed
Saito,
Melk-like kinase plays a role in hematopoiesis in the zebra fish.
2005,
Pubmed
Vulsteke,
Inhibition of spliceosome assembly by the cell cycle-regulated protein kinase MELK and involvement of splicing factor NIPP1.
2004,
Pubmed
Whitfield,
Identification of genes periodically expressed in the human cell cycle and their expression in tumors.
2002,
Pubmed