<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Hergovich A</dc:creator>
  <dc:creator>Lamla S</dc:creator>
  <dc:creator>Nigg EA</dc:creator>
  <dc:creator>Hemmings BA</dc:creator>
  <dc:date>2007</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Human NDR kinases are upregulated in some cancer types, yet their functions still remain undefined. Here, we report the first known function of a mammalian NDR kinase by demonstrating that human NDR directly contributes to centrosome duplication. A subpopulation of endogenous NDR localizes to centrosomes in a cell-cycle-dependent manner. Overexpression of NDR resulted in centrosome overduplication in a kinase-activity-dependent manner, while expression of kinase-dead NDR or depletion of NDR by small interfering RNA (siRNA) negatively affected centrosome duplication. By targeting NDR to the centrosome, we show that the centrosomal pool of NDR is sufficient to generate supernumerary centrosomes. Furthermore, our data indicate that NDR-driven centrosome duplication requires Cdk2 activity and that Cdk2-induced centrosome amplification is affected upon reduction of NDR activity. Overall, considering that centrosome overduplication is linked to cellular transformation, our observations may also provide a molecular link between mammalian NDR kinases and cancer.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/205482</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molcel.2007.01.020</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/17317633</dc:relation>
  <dc:source>Molecular cell. - 2007</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">CHO Cells</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">COS Cells</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Centrosome</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Chlorocebus aethiops</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Cricetinae</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Cricetulus</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Cyclin-Dependent Kinase 2</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Gene Expression</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">HCT116 Cells</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">HeLa Cells</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">NIH 3T3 Cells</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Protein Binding</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Protein Transport</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Protein-Serine-Threonine Kinases</dc:subject>
  <dc:title xmlns:ns18="xml" ns18:lang="en">Centrosome-associated NDR kinase regulates centrosome duplication.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
