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The DASH complex and Klp5/Klp6 kinesin coordinate bipolar chromosome attachment in fission yeast
Author(s) -
SanchezPerez Isabel,
Renwick Steven J,
Crawley Karen,
Karig Inga,
Buck Vicky,
Meadows John C,
FrancoSanchez Alejandro,
Fleig Ursula,
Toda Takashi,
Millar Jonathan B A
Publication year - 2005
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7600761
Subject(s) - obituary , library science , biology , political science , law , computer science
We identified a truncated allele of dam1 as a multicopy suppressor of the sensitivity of cdc13‐117 (cyclin B) and mal3‐1 (EB‐1) cells to thiabendazole, a microtubule poison. We find that Dam1 binds to the plus end of spindle microtubules and kinetochores as cells enter mitosis and this is dependent on other components of the fission yeast DASH complex, including Ask1, Duo1, Spc34 and Dad1. By contrast, Dad1 remains bound to kinetochores throughout the cell cycle and its association is dependent on the Mis6 and Mal2, but not Mis12, Nuf2 or Cnp1, kinetochore proteins. In cells lacking Dam1, or other components of the DASH complex, anaphase is delayed due to activation of the spindle assembly checkpoint and lagging sister chromatids are frequently observed and occasionally sister chromatid pairs segregate to the same spindle pole. We find that the mitotic centromere‐associated Klp5/Klp6 kinesin complex is essential in cells lacking components of the DASH complex. Cells lacking both Dam1 and Klp5 undergo a first cell cycle arrest in mitosis due to a failure to establish bipolar chromosome attachment.