TY - JOUR
T1 - Uncoupling the central spindle-associated function of the chromosomal passenger complex from its role at centromeres
AU - Lens, Susanne M A
AU - Rodriguez, Jose A
AU - Vader, Gerben
AU - Span, Simone W
AU - Giaccone, Giuseppe
AU - Medema, René H
PY - 2006/4
Y1 - 2006/4
N2 - Survivin is a component of the chromosomal passenger complex (CPC) that plays a role in maintenance of an active spindle checkpoint and in cytokinesis. To study whether these different functions can be attributed to distinct domains within the Survivin protein, we complemented Survivin-depleted cells with a variety of point- and deletion-mutants of Survivin. We show that an intact baculovirus IAP repeat (BIR) domain is required for proper spindle checkpoint functioning, but dispensable for cytokinesis. In line with this, mutants lacking an intact BIR domain localized normally to the central spindle, but their localization to inner centromeres was severely perturbed. Consequently, these mutants failed to recruit Aurora B, Borealin/Dasra B, and BubR1 to centromeres and kinetochores, but they had retained the ability to recruit Aurora B and Borealin/Dasra B to the midzone and midbody. Thus, the C terminus of Survivin is sufficient for central spindle localization and execution of cytokinesis, but the additional presence of a functional BIR domain is essential for centromere targeting and spindle checkpoint function. Importantly, our data show that the function of the CPC at the centromere can be separated from its function at the central spindle and that execution of cytokinesis does not require prior concentration of the CPC at centromeres.
AB - Survivin is a component of the chromosomal passenger complex (CPC) that plays a role in maintenance of an active spindle checkpoint and in cytokinesis. To study whether these different functions can be attributed to distinct domains within the Survivin protein, we complemented Survivin-depleted cells with a variety of point- and deletion-mutants of Survivin. We show that an intact baculovirus IAP repeat (BIR) domain is required for proper spindle checkpoint functioning, but dispensable for cytokinesis. In line with this, mutants lacking an intact BIR domain localized normally to the central spindle, but their localization to inner centromeres was severely perturbed. Consequently, these mutants failed to recruit Aurora B, Borealin/Dasra B, and BubR1 to centromeres and kinetochores, but they had retained the ability to recruit Aurora B and Borealin/Dasra B to the midzone and midbody. Thus, the C terminus of Survivin is sufficient for central spindle localization and execution of cytokinesis, but the additional presence of a functional BIR domain is essential for centromere targeting and spindle checkpoint function. Importantly, our data show that the function of the CPC at the centromere can be separated from its function at the central spindle and that execution of cytokinesis does not require prior concentration of the CPC at centromeres.
KW - Aurora Kinase B
KW - Aurora Kinases
KW - Cell Cycle Proteins/metabolism
KW - Centromere/chemistry
KW - Chromosomal Proteins, Non-Histone/analysis
KW - Chromosomes, Human/metabolism
KW - Cytokinesis/genetics
KW - DNA Mutational Analysis
KW - Humans
KW - Inhibitor of Apoptosis Proteins
KW - Kinetochores/metabolism
KW - Microtubule-Associated Proteins/analysis
KW - Neoplasm Proteins/analysis
KW - Point Mutation
KW - Protein Kinases/metabolism
KW - Protein Serine-Threonine Kinases/analysis
KW - Protein Structure, Tertiary/genetics
KW - RNA, Small Interfering/genetics
KW - Sequence Deletion
KW - Spindle Apparatus/chemistry
KW - Survivin
U2 - 10.1091/mbc.e05-08-0727
DO - 10.1091/mbc.e05-08-0727
M3 - Article
C2 - 16436504
SN - 1059-1524
VL - 17
SP - 1897
EP - 1909
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 4
ER -