TY - JOUR
T1 - CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore-microtubule attachment
AU - Itoh, Go
AU - Kanno, Shin Ichiro
AU - Uchida, Kazuhiko S.K.
AU - Chiba, Shuhei
AU - Sugino, Shiro
AU - Watanabe, Kana
AU - Mizuno, Kensaku
AU - Yasui, Akira
AU - Hirota, Toru
AU - Tanaka, Kozo
PY - 2011/1/5
Y1 - 2011/1/5
N2 - Proper attachment of microtubules to kinetochores is essential for accurate chromosome segregation. Here, we report a novel protein involved in kinetochore-microtubule attachment, chromosome alignment-maintaining phosphoprotein (CAMP) (C13orf8, ZNF828). CAMP is a zinc-finger protein containing three characteristic repeat motifs termed the WK, SPE, and FPE motifs. CAMP localizes to chromosomes and the spindle including kinetochores, and undergoes CDK1-dependent phosphorylation at multiple sites during mitosis. CAMP-depleted cells showed severe chromosome misalignment, which was associated with the poor resistance of K-fibres to the tension exerted upon establishment of sister kinetochore bi-orientation. We found that the FPE region, which is responsible for spindle and kinetochore localization, is essential for proper chromosome alignment. The C-terminal region containing the zinc-finger domains negatively regulates chromosome alignment, and phosphorylation in the FPE region counteracts this regulation. Kinetochore localization of CENP-E and CENP-F was affected by CAMP depletion, and by expressing CAMP mutants that cannot functionally rescue CAMP depletion, placing CENP-E and CENP-F as downstream effectors of CAMP. These data suggest that CAMP is required for maintaining kinetochore-microtubule attachment during bi-orientation.
AB - Proper attachment of microtubules to kinetochores is essential for accurate chromosome segregation. Here, we report a novel protein involved in kinetochore-microtubule attachment, chromosome alignment-maintaining phosphoprotein (CAMP) (C13orf8, ZNF828). CAMP is a zinc-finger protein containing three characteristic repeat motifs termed the WK, SPE, and FPE motifs. CAMP localizes to chromosomes and the spindle including kinetochores, and undergoes CDK1-dependent phosphorylation at multiple sites during mitosis. CAMP-depleted cells showed severe chromosome misalignment, which was associated with the poor resistance of K-fibres to the tension exerted upon establishment of sister kinetochore bi-orientation. We found that the FPE region, which is responsible for spindle and kinetochore localization, is essential for proper chromosome alignment. The C-terminal region containing the zinc-finger domains negatively regulates chromosome alignment, and phosphorylation in the FPE region counteracts this regulation. Kinetochore localization of CENP-E and CENP-F was affected by CAMP depletion, and by expressing CAMP mutants that cannot functionally rescue CAMP depletion, placing CENP-E and CENP-F as downstream effectors of CAMP. These data suggest that CAMP is required for maintaining kinetochore-microtubule attachment during bi-orientation.
KW - chromosome
KW - kinetochore
KW - metaphase
KW - microtubule
KW - spindle
UR - http://www.scopus.com/inward/record.url?scp=78650889802&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78650889802&partnerID=8YFLogxK
U2 - 10.1038/emboj.2010.276
DO - 10.1038/emboj.2010.276
M3 - Article
C2 - 21063390
AN - SCOPUS:78650889802
SN - 0261-4189
VL - 30
SP - 130
EP - 144
JO - EMBO Journal
JF - EMBO Journal
IS - 1
ER -