CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore-microtubule attachment

被引:52
作者
Itoh, Go
Kanno, Shin-ichiro [2 ]
Uchida, Kazuhiko S. K. [3 ]
Chiba, Shuhei [4 ]
Sugino, Shiro
Watanabe, Kana
Mizuno, Kensaku [4 ]
Yasui, Akira [2 ]
Hirota, Toru [3 ]
Tanaka, Kozo [1 ]
机构
[1] Tohoku Univ, Inst Dev Aging & Canc, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Inst Dev Aging & Canc, Div Dynam Proteome Aging & Canc, Sendai, Miyagi 9808575, Japan
[3] Japanese Fdn Canc Res, Inst Canc, Div Expt Pathol, Tokyo 170, Japan
[4] Tohoku Univ, Grad Sch Life Sci, Dept Biomol Sci, Sendai, Miyagi 9808575, Japan
基金
日本科学技术振兴机构;
关键词
chromosome; kinetochore; metaphase; microtubule; spindle; CENP-F; CHROMOSOME ALIGNMENT; FIBERS CONTRIBUTES; MITOTIC CHECKPOINT; SPINDLE DYNAMICS; ANAPHASE ONSET; SKA COMPLEX; PROTEIN; CAPTURE; PROGRESSION;
D O I
10.1038/emboj.2010.276
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proper attachment of microtubules to kinetochores is essential for accurate chromosome segregation. Here, we report a novel protein involved in kinetochore-tnicrotubule 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. The EMBO Journal (2011) 30, 130-144. doi:10.1038/emboj.2010.276; Published online 9 November 2010
引用
收藏
页码:130 / 144
页数:15
相关论文
共 70 条
[1]   The Dam1 kinetochore complex harnesses microtubule dynamics to produce force and movement [J].
Asbury, Charles L. ;
Gestaut, Daniel R. ;
Powers, Andrew F. ;
Franck, Andrew D. ;
Davis, Trisha N. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (26) :9873-9878
[2]   Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules [J].
Ashar, HR ;
James, L ;
Gray, K ;
Carr, D ;
Black, S ;
Armstrong, L ;
Bishop, WR ;
Kirschmeier, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) :30451-30457
[3]   Mitotic regulation of the anaphase-promoting complex [J].
Baker, D. J. ;
Dawlaty, M. M. ;
Galardy, P. ;
van Deursen, J. M. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (05) :589-600
[4]   Unstable microtubule capture at kinetochores depleted of the centromere-associated protein CENP-F [J].
Bomont, P ;
Maddox, P ;
Shah, JV ;
Desai, AB ;
Cleveland, DW .
EMBO JOURNAL, 2005, 24 (22) :3927-3939
[5]   Characterization of MAD2B and other mitotic spindle checkpoint genes [J].
Cahill, DP ;
da Costa, LT ;
Carson-Walter, EB ;
Kinzler, KW ;
Vogelstein, B ;
Lengauer, C .
GENOMICS, 1999, 58 (02) :181-187
[6]   TOGp, the human homolog of XMAP215/Dis1, is required for centrosome integrity, spindle pole organization, and bipolar spindle assembly [J].
Cassimeris, L ;
Morabito, J .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (04) :1580-1590
[7]   Characterization of the kinetochore binding domain of CENP-E reveals interactions with the kinetochore proteins CENP-F and hBUBR1 [J].
Chan, GKT ;
Schaar, BT ;
Yen, TJ .
JOURNAL OF CELL BIOLOGY, 1998, 143 (01) :49-63
[8]   Molecular architecture of the kinetochore-microtubule interface [J].
Cheeseman, Iain M. ;
Desai, Arshad .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (01) :33-46
[9]   The conserved KMN network constitutes the core microtubule-binding site of the kinetochore [J].
Cheeseman, Iain M. ;
Chappie, Joshua S. ;
Wilson-Kubalek, Elizabeth M. ;
Desai, Arshad .
CELL, 2006, 127 (05) :983-997
[10]   MAD2B is an inhibitor of the anaphase-promoting complex [J].
Chen, J ;
Fang, GW .
GENES & DEVELOPMENT, 2001, 15 (14) :1765-1770