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Determinants for activation of the atypical AGC kinase Greatwall during M phase entry.


ABSTRACT: The atypical AGC kinase Greatwall (Gwl) mediates a pathway that prevents the precocious removal of phosphorylations added to target proteins by M phase-promoting factor (MPF); Gwl is thus essential for M phase entry and maintenance. Gwl itself is activated by M phase-specific phosphorylations that are investigated here. Many phosphorylations are nonessential, being located within a long nonconserved region, any part of which can be deleted without effect. Using mass spectrometry and mutagenesis, we have identified 3 phosphorylation sites (phosphosites) critical to Gwl activation (pT193, pT206, and pS883 in Xenopus laevis) located in evolutionarily conserved domains that differentiate Gwl from related kinases. We propose a model in which the initiating event for Gwl activation is phosphorylation by MPF of the proline-directed sites T193 and T206 in the presumptive activation loop. After this priming step, Gwl can intramolecularly phosphorylate its C-terminal tail at pS883; this site probably plays a role similar to that of the tail/Z motif of other AGC kinases. These events largely (but not completely) explain the full activation of Gwl at M phase.

SUBMITTER: Blake-Hodek KA 

PROVIDER: S-EPMC3318580 | biostudies-literature | 2012 Apr

REPOSITORIES: biostudies-literature

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Determinants for activation of the atypical AGC kinase Greatwall during M phase entry.

Blake-Hodek Kristina A KA   Williams Byron C BC   Zhao Yong Y   Castilho Priscila V PV   Chen Wei W   Mao Yuxin Y   Yamamoto Tomomi M TM   Goldberg Michael L ML  

Molecular and cellular biology 20120221 8


The atypical AGC kinase Greatwall (Gwl) mediates a pathway that prevents the precocious removal of phosphorylations added to target proteins by M phase-promoting factor (MPF); Gwl is thus essential for M phase entry and maintenance. Gwl itself is activated by M phase-specific phosphorylations that are investigated here. Many phosphorylations are nonessential, being located within a long nonconserved region, any part of which can be deleted without effect. Using mass spectrometry and mutagenesis  ...[more]

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