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The highly abundant AAA-ATPase p97 is required for diverse cellular processes, of which ER-associated protein degradation (ERAD) is understood best. Previously, a new role of p97 in spindle disassembly at the end of mitosis has been reported. However, we show that neither addition of dominant-negative p97 mutants nor depletion of crucial p97 adaptors impairs transition of meiotic spindles into interphase arrays of microtubules. The dominant-negative approach is validated by inhibition of ERAD, which we reconstitute for the first time in the powerful biochemical system of Xenopus egg extracts. The role of p97 in spindle disassembly during meiotic exit should therefore be reconsidered.
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JCS ePress
online publication date 20 Mar 2007
doi: 10.1242/jcs.006924
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120/8/1325
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The AAA-ATPase p97-Ufd1-Npl4 is required for ERAD but not for spindle disassembly in Xenopus egg extracts
* Author for correspondence (e-mail: stemmann{at}biochem.mpg.de)
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J. Mouysset, A. Deichsel, S. Moser, C. Hoege, A. A. Hyman, A. Gartner, and T. Hoppe
Cell cycle progression requires the CDC-48UFD-1/NPL-4 complex for efficient DNA replication
PNAS,
September 2, 2008;
105(35):
12879 - 12884.
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© The Company of Biologists Ltd 2007