The role of centromere-binding factor 3 (CBF3) in spindle stability, cytokinesis, and kinetochore attachment

2005 ◽  
Vol 83 (6) ◽  
pp. 696-702 ◽  
Author(s):  
David Bouck ◽  
Kerry Bloom
Keyword(s):  
Essential Role ◽  
Anaphase Onset ◽  
Binding Factor ◽  
Chromosomal Passenger ◽  
Chromosomal Passenger Proteins ◽  
Spindle Midzone ◽  
Spindle Stability ◽  
Passenger Proteins ◽  
Passenger Protein

The spindle midzone is critical for spindle stability and cytokinesis. Chromosomal passenger proteins relocalize from chromosomes to the spindle midzone after anaphase onset. The recent localization of the inner-kinetochore, centromere-binding factor 3 (CBF3) complex to the spindle midzone in budding yeast has led to the discovery of novel functions for this complex in addition to its essential role at kinetochores. In G1/S cells, CBF3 components are detected along dynamic microtubules, where they can "search-and-capture" newly replicated centromeres. During anaphase, CBF3 is transported to the microtubule plus-ends of the spindle midzone. Consistent with this localization, cells containing a mutation in the CBF3 subunit Ndc10p show defects in spindle stability during anaphase. In addition, ndc10-1 cells show defects during cytokinesis, resulting in a defect in cell abscission. These results highlight the importance of midzone-targeted proteins in coordinating mitosis with cell division. Here we discuss these findings and explore the significance of CBF3 transport to microtubule plus-ends at the spindle midzone.Key words: spindle midzone, passenger protein, inner centromere protein (INCENP), microtubule plus-end.

scholarly journals Contractile Ring-independent Localization of DdINCENP, a Protein Important for Spindle Stability and Cytokinesis

2006 ◽  
Vol 17 (2) ◽  
pp. 779-788 ◽  
Author(s):  
Qian Chen ◽  
Hui Li ◽  
Arturo De Lozanne
Keyword(s):  
Myosin Ii ◽  
Cleavage Furrow ◽  
Contractile Ring ◽  
Subsequent Formation ◽  
Daughter Cells ◽  
Chromosomal Passenger ◽  
Spindle Midzone ◽  
Spindle Stability ◽  
Passenger Protein

Dictyostelium DdINCENP is a chromosomal passenger protein associated with centromeres, the spindle midzone, and poles during mitosis and the cleavage furrow during cytokinesis. Disruption of the single DdINCENP gene revealed important roles for this protein in mitosis and cytokinesis. DdINCENP null cells lack a robust spindle midzone and are hypersensitive to microtubule-depolymerizing drugs, suggesting that their spindles may not be stable. Furthermore DdCP224, a protein homologous to the microtubule-stabilizing protein TOGp/XMAP215, was absent from the spindle midzone of DdINCENP null cells. Overexpression of DdCP224 rescued the weak spindle midzone defect of DdINCENP null cells. Although not required for the localization of the myosin II contractile ring and subsequent formation of a cleavage furrow, DdINCENP is important for the abscission of daughter cells at the end of cytokinesis. Finally, we show that the localization of DdINCENP at the cleavage furrow is modulated by myosin II but it occurs by a mechanism different from that controlling the formation of the contractile ring.

scholarly journals Bir1 Is Required for the Tension Checkpoint

2009 ◽  
Vol 20 (3) ◽  
pp. 915-923 ◽  
Author(s):  
Michelle M. Shimogawa ◽  
Per O. Widlund ◽  
Michael Riffle ◽  
Michael Ess ◽  
Trisha N. Davis
Keyword(s):  
Aurora B ◽  
Temperature Sensitive ◽  
Sensitive Mutant ◽  
Checkpoint Response ◽  
Temperature Sensitive Mutant ◽  
The Third ◽  
Chromosomal Passenger ◽  
Chromosomal Passenger Proteins ◽  
Passenger Proteins

The Saccharomyces cerevisiae chromosomal passenger proteins Ipl1 (Aurora B) and Sli15 (INCENP) are required for the tension checkpoint, but the role of the third passenger, Bir1, is controversial. We have isolated a temperature-sensitive mutant (bir1-107) in the essential C-terminal region of Bir1 known to be required for binding to Sli15. This allele reveals a checkpoint function for Bir1. The mutant displays a biorientation defect, a defective checkpoint response to lack of tension, and an inability to detach mutant kinetochores. Ipl1 localizes to aberrant foci when Bir1 localization is disrupted in the bir1-107 mutant. Thus, one checkpoint role of Bir1 is to properly localize Ipl1 and allow detachment of kinetochores. Quantitative analysis indicates that the chromosomal passengers colocalize with kinetochores in G1 but localize between kinetochores that are under tension. Bir1 localization to kinetochores is maintained in an mcd1-1 mutant in the absence of tension. Our results suggest that the establishment of tension removes Ipl1, Bir1, and Sli15, and their kinetochore detachment activity, from the vicinity of kinetochores and allows cells to proceed through the tension checkpoint.

scholarly journals The Mitotic Exit Network Mob1p-Dbf2p Kinase Complex Localizes to the Nucleus and Regulates Passenger Protein Localization

2005 ◽  
Vol 16 (12) ◽  
pp. 5465-5479 ◽  
Author(s):  
Jan Stoepel ◽  
Michelle A. Ottey ◽  
Cornelia Kurischko ◽  
Philip Hieter ◽  
Francis C. Luca
Keyword(s):  
Chromatin Immunoprecipitation ◽  
Protein Localization ◽  
Mitotic Exit ◽  
Mitotic Exit Network ◽  
Chromosomal Passenger ◽  
Early Anaphase ◽  
Chromosomal Passenger Proteins ◽  
Kinetochore Region ◽  
Passenger Proteins ◽  
Passenger Protein

The Saccharomyces cerevisiae mitotic exit network (MEN) is a conserved signaling network that coordinates CDK inactivation, cytokinesis and G1 gene transcription. The MEN Cdc14p phosphatase is sequestered in the nucleolus and transiently released in early anaphase and telophase. Cdc14p mediates mitotic exit by dephosphorylating Cdk1p substrates and promoting Cdk1p inactivation. Cdc14p also regulates the localization of chromosomal passenger proteins, which redistribute from kinetochores to the mitotic spindle during anaphase. Here we present evidence that the MEN protein kinase complex Mob1p-Dbf2p localizes to mitotic nuclei and partially colocalizes with Cdc14p and kinetochore proteins. Chromatin immunoprecipitation (ChIP) experiments reveal that Mob1p, Dbf2p, and Cdc14p associate with centromere DNA and require the centromere binding protein Ndc10p for this association. We establish that Mob1p is essential for maintaining the localization of Aurora, INCENP, and Survivin chromosomal passenger proteins on anaphase spindles, whereas Cdc14p and the Mob1p-Dbf2p-activating kinase Cdc15p are required for establishing passenger protein localization on the spindle. Moreover, Mob1p, but not Cdc15p, is required for dissociating Aurora from the kinetochore region. These findings reveal kinetochores as sites for MEN signaling and implicate MEN in coordinating chromosome segregation and/or spindle integrity with mitotic exit and cytokinesis via regulation of chromosome passenger proteins.

Aurora-B Kinase Translocates to the Midzone in Endomitotic Megakaryocytes.

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 1263-1263
Author(s):  
Amy E. Geddis ◽  
Kenneth Kaushansky
Keyword(s):  
Actin Dynamics ◽  
Aurora B ◽  
Cleavage Furrow ◽  
Aurora B Kinase ◽  
Metaphase Chromosomes ◽  
Late Anaphase ◽  
Chromosomal Passenger ◽  
Chromosomal Passenger Proteins ◽  
Spindle Midzone ◽  
Passenger Proteins

Abstract Megakaryocyte (MK) differentiation is marked by the development of progressive polyploidy, facilitating platelet production by the creation of a large cytoplasmic volume. MKs become polyploid through repeated cycles of endomitosis (EnM), in which mitosis is initiated but subsequently aborted in late anaphase with failure to complete karyokinesis and cytokinesis. However, the mechanisms underlying EnM remain poorly understood. Recent hypotheses explored in the literature have focused on the possible absence or mislocalization of the chromosomal passenger protein Aurora-B kinase, as it has a pivotal role in many aspects of cytokinesis. Along with the other passenger proteins, Aurora-B kinase transits from the centromeres of metaphase chromosomes to the bundled microtubules of the spindle midzone and overlying cortex between separating chromosomes in anaphase. The midzone and its associated proteins, are thought to be critical for determining the position of the cleavage furrow. One of these proteins, the kinesin MKLP-2, is required for the translocation of Aurora-B kinase to the midzone, where it co-localizes with the GTPase MgcRacGAP and stimulates its activity towards RhoA, potentially regulating actin dynamics at the cleavage furrow. We have previously demonstrated that several chromosomal passenger proteins including Aurora-B kinase are normally expressed and localized to centromeres in EnM MKs. In this work, we use deconvolution microscopy in primary murine and human MKs to extend those findings and demonstrate that EnM MKs form midzone structures that are characteristic of late anaphase; in addition, Aurora-B kinase is clearly present on the spindle midzone, as are MKLP-2 and MgcRacGAP. Although we found images suggestive of initial cleavage furrow formation with cortical localization of Aurora-B kinase in late phase cells, we were unable to demonstrate enhanced localization of actin or anillin to the furrow in EnM cells, despite their normal localization in diploid control cells. Therefore, many of the components of the central spindle are intact during MK EnM, but the formation of the cleavage furrow appears to be incomplete. These data add to our understanding of the possible mechanisms underlying EnM and offer an alternative hypothesis to that of failed expression or localization of the chromosomal passenger proteins. Ongoing studies will focus on the assembly and function of the cleavage furrow in this enigmatic process.

scholarly journals Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly

2018 ◽  
Vol 217 (5) ◽  
pp. 1687-1700 ◽  
Author(s):  
Itziar Ibarlucea-Benitez ◽  
Luke S. Ferro ◽  
David G. Drubin ◽  
Georjana Barnes
Keyword(s):  
Single Molecule ◽  
Molecular Mechanisms ◽  
Chromosomal Passenger Complex ◽  
Late Anaphase ◽  
Chromosomal Passenger ◽  
Spindle Disassembly ◽  
Spindle Midzone ◽  
Chromosome Separation

Mitotic spindle disassembly after chromosome separation is as important as spindle assembly, yet the molecular mechanisms for spindle disassembly are unclear. In this study, we investigated how the chromosomal passenger complex (CPC), which contains the Aurora B kinase Ipl1, swiftly concentrates at the spindle midzone in late anaphase, and we researched the role of this dramatic relocalization during spindle disassembly. We showed that the kinesins Kip1 and Kip3 are essential for CPC relocalization. In cells lacking Kip1 and Kip3, spindle disassembly is severely delayed until after contraction of the cytokinetic ring. Purified Kip1 and Kip3 interact directly with the CPC and recruit it to microtubules in vitro, and single-molecule experiments showed that the CPC diffuses dynamically on microtubules but that diffusion stops when the CPC encounters a Kip1 molecule. We propose that Kip1 and Kip3 trap the CPC at the spindle midzone in late anaphase to ensure timely spindle disassembly.

scholarly journals Use of DT40 conditional-knockout cell lines to study chromosomal passenger protein function

2010 ◽  
Vol 38 (6) ◽  
pp. 1655-1659 ◽  
Author(s):  
Xavier Fant ◽  
Kumiko Samejima ◽  
Ana Carvalho ◽  
Hiromi Ogawa ◽  
Zhenjie Xu ◽  
...  
Keyword(s):  
Cell Lines ◽  
Protein Function ◽  
Kinase Activity ◽  
Current Knowledge ◽  
Conditional Knockout ◽  
Aurora B ◽  
Aurora B Kinase ◽  
Chromosomal Passenger ◽  
Passenger Protein

The CPC [chromosomal passenger complex; INCENP (inner centromere protein), Aurora B kinase, survivin and borealin] is implicated in many mitotic processes. In the present paper we describe how we generated DT40 conditional-knockout cell lines for incenp1 and survivin1 to better understand the role of these CPC subunits in the control of Aurora B kinase activity. These lines enabled us to reassess current knowledge of survivin function and to show that INCENP acts as a rheostat for Aurora B activity.

scholarly journals Both midzone and astral microtubules are involved in the delivery of cytokinesis signals

2002 ◽  
Vol 159 (1) ◽  
pp. 45-53 ◽  
Author(s):  
Maki Murata-Hori ◽  
Yu-li Wang
Keyword(s):  
Signaling Pathway ◽  
Cultured Cells ◽  
Aurora B ◽  
Anaphase Onset ◽  
Cytoplasmic Proteins ◽  
Chromosomal Passenger ◽  
Dynamic Exchange ◽  
Passenger Protein

To address the mechanism that coordinates cytokinesis with mitosis, we have studied the dynamics of aurora B, a chromosomal passenger protein involved in signaling cytokinesis. Photobleaching analyses indicated dynamic exchange of aurora B between a centromeric and a cytoplasmic pool before anaphase onset, and stable associations with microtubules after anaphase onset. Bleaching near centromeres upon anaphase onset affected the subsequent appearance of fluorescence along midzone microtubules, but not that near the lateral equatorial cortex, suggesting that there were centromeric-dependent and -independent pathways that transported aurora B to the equator. The former delivered centromeric aurora B along midzone microtubules, whereas the latter delivered cytoplasmic aurora B along astral microtubules. We suggest that cultured cells use midzone microtubules as the primary signaling pathway for cytokinesis, whereas embryos, with their stockpile of cytoplasmic proteins and large sizes, rely primarily on astral microtubules.

scholarly journals Shugoshin 2 Regulates Localization of the Chromosomal Passenger Proteins in Fission Yeast Mitosis

2007 ◽  
Vol 18 (5) ◽  
pp. 1657-1669 ◽  
Author(s):  
Vincent Vanoosthuyse ◽  
Sergey Prykhozhij ◽  
Kevin G. Hardwick
Keyword(s):  
Fission Yeast ◽  
Spindle Checkpoint ◽  
Aurora B ◽  
Checkpoint Activation ◽  
C Terminus ◽  
Chromosomal Passenger ◽  
Chromosomal Passenger Proteins ◽  
Passenger Proteins ◽  
Meiosis I ◽  
Mitotic Cells

Fission yeast has two members of the Shugoshin family, Sgo1 and Sgo2. Although Sgo1 has clearly been established as a protector of centromere cohesion in meiosis I, the roles of Sgo2 remain elusive. Here we show that Sgo2 is required to ensure proper chromosome biorientation upon recovery from a prolonged spindle checkpoint arrest. Consistent with this, Sgo2 is essential for maintaining the Passenger proteins on centromeres upon checkpoint activation. Interestingly, lack of Sgo2 has a more penetrant effect on the localization of Survivin than on the two other Passenger proteins INCENP and Aurora B, and the Survivin-INCENP complex but not the INCENP-Aurora B complex is destabilized in the absence of Sgo2. Finally we show that the conserved C-terminus of Sgo2 is crucial to maintain Sgo2 and Passenger proteins localization on centromeres upon prolonged checkpoint activation. Taken together, our results demonstrate that Sgo2 is important for chromosome biorientation and that it controls docking of the Passenger proteins on chromosomes in early mitotic cells.

Analysis of the distribution of the INCENPs throughout mitosis reveals the existence of a pathway of structural changes in the chromosomes during metaphase and early events in cleavage furrow formation

1991 ◽  
Vol 98 (4) ◽  
pp. 443-461 ◽  
Author(s):  
W.C. Earnshaw ◽  
C.A. Cooke
Keyword(s):  
Structural Changes ◽  
Metaphase Plate ◽  
Maximum Diameter ◽  
Cell Cortex ◽  
Cleavage Furrow ◽  
Intracellular Location ◽  
Chromosomal Passenger ◽  
Early Anaphase ◽  
Chromosomal Passenger Proteins ◽  
Passenger Proteins

The INCENPs are two polypeptides of 135 × 10(3) and 150 × 10(3) Mr that enter mitosis as tightly bound chromosomal proteins, but subsequently leave the chromosomes altogether and become associated with the central spindle and cell cortex at the contractile ring. In the experiments reported here we have used confocal microscopy and immunoelectron microscopy to provide a detailed picture of the intracellular location of these proteins during mitosis. The experiments have not only revealed a number of new details concerning the properties of the INCENPs in mitosis, but have revealed a number of novel aspects of the mitotic process itself. The first of these is the existence of a sequential pathway of structural changes in the chromosomes that occurs during metaphase. This pathway is revealed by the existence of four distinct INCENP staining patterns in mitotic cells. In ‘early’ and ‘early/mid’ metaphase, the INCENPs gradually become concentrated at the centromeres, forming a ring at the center of the metaphase plate. During ‘mid/late’ metaphase they exit from the chromosomes, so that by late metaphase they are found solely in streaks that traverse the plate parallel to the spindle axis. The streaks probably correspond to INCENPs closely associated with microtubule bundles, perhaps as part of the stem body material. Examination of transverse optical sections of the spindle interzone during early anaphase reveals an unexpectedly high degree of order. The INCENP antigens are localized on fibers that are organized into a hollow ring 8 microns in diameter and approximately 4 microns beneath the cell cortex. Measurement of cellular dimensions in the confocal microscope reveals that the maximum diameter of early anaphase cells lies across the spindle equator, so that when the cleavage furrow forms, it does so around the maximum circumference of the cell. During anaphase, a subpopulation of the INCENP antigen becomes localized to the cortex where the furrow will subsequently form. This occurs prior to any other evidence of furrowing. Thus, binding of the INCENPs to this region may represent an early step in furrow formation. Together, these results suggest that the INCENPs may represent a new class of ‘chromosomal passenger’ proteins that are carried to the spindle equator by the chromosomes and subsequently perform a cytoskeletal role following their release from the chromosomes at the metaphase:anaphase transition.

Sign in / Sign up

Export Citation Format

Share Document