scholarly journals NACK Kinesin Is Required for Metaphase Chromosome Alignment and Cytokinesis in the Moss Physcomitrella Patens

2015 ◽  
Vol 40 (1) ◽  
pp. 31-41 ◽  
Author(s):  
Haruko Naito ◽  
Gohta Goshima
2011 ◽  
Vol 20 (3) ◽  
pp. 342-352 ◽  
Author(s):  
Lina Cheng ◽  
Jiayin Zhang ◽  
Sana Ahmad ◽  
Lorene Rozier ◽  
Haiqian Yu ◽  
...  

2007 ◽  
Vol 179 (2) ◽  
pp. 357-357
Author(s):  
Jiayin Zhang ◽  
Sana Ahmad ◽  
Yinghui Mao

2000 ◽  
Vol 150 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Jennifer K. Yucel ◽  
Janet D. Marszalek ◽  
J. Richard McIntosh ◽  
Lawrence S.B. Goldstein ◽  
Don W. Cleveland ◽  
...  

CENP-meta has been identified as an essential, kinesin-like motor protein in Drosophila. The 257-kD CENP-meta protein is most similar to the vertebrate kinetochore-associated kinesin-like protein CENP-E, and like CENP-E, is shown to be a component of centromeric/kinetochore regions of Drosophila chromosomes. However, unlike CENP-E, which leaves the centromere/kinetochore region at the end of anaphase A, the CENP-meta protein remains associated with the centromeric/kinetochore region of the chromosome during all stages of the Drosophila cell cycle. P-element–mediated disruption of the CENP-meta gene leads to late larval/pupal stage lethality with incomplete chromosome alignment at metaphase. Complete removal of CENP-meta from the female germline leads to lethality in early embryos resulting from defects in metaphase chromosome alignment. Real-time imaging of these mutants with GFP-labeled chromosomes demonstrates that CENP-meta is required for the maintenance of chromosomes at the metaphase plate, demonstrating that the functions required to establish and maintain chromosome congression have distinguishable requirements.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Mihaela Jagrić ◽  
Patrik Risteski ◽  
Jelena Martinčić ◽  
Ana Milas ◽  
Iva M Tolić

During metaphase, chromosome position at the spindle equator is regulated by the forces exerted by kinetochore microtubules and polar ejection forces. However, the role of forces arising from mechanical coupling of sister kinetochore fibers with bridging fibers in chromosome alignment is unknown. Here we develop an optogenetic approach for acute removal of PRC1 to partially disassemble bridging fibers and show that they promote chromosome alignment. Tracking of the plus-end protein EB3 revealed longer antiparallel overlaps of bridging microtubules upon PRC1 removal, which was accompanied by misaligned and lagging kinetochores. Kif4A/kinesin-4 and Kif18A/kinesin-8 were found within the bridging fiber and largely lost upon PRC1 removal, suggesting that these proteins regulate the overlap length of bridging microtubules. We propose that PRC1-mediated crosslinking of bridging microtubules and recruitment of kinesins to the bridging fiber promotes chromosome alignment by overlap length-dependent forces transmitted to the associated kinetochore fibers.


Cell Cycle ◽  
2005 ◽  
Vol 4 (5) ◽  
pp. 665-668 ◽  
Author(s):  
Jun Dai ◽  
Jonathan M.G. Higgins

2009 ◽  
Vol 187 (6) ◽  
pp. 754-755
Author(s):  
Caitlin Sedwick

Kapoor uses small molecule inhibitors and high-resolution microscopy to explore metaphase chromosome alignment.


2013 ◽  
Vol 49 (6) ◽  
pp. 1097-1107 ◽  
Author(s):  
Lorene Rozier ◽  
Yige Guo ◽  
Shaun Peterson ◽  
Mai Sato ◽  
Richard Baer ◽  
...  

2012 ◽  
Vol 199 (2) ◽  
pp. 251-268 ◽  
Author(s):  
Fangwei Wang ◽  
Natalia P. Ulyanova ◽  
John R. Daum ◽  
Debasis Patnaik ◽  
Anna V. Kateneva ◽  
...  

Haspin phosphorylates histone H3 at threonine-3 (H3T3ph), providing a docking site for the Aurora B complex at centromeres. Aurora B functions to correct improper kinetochore–microtubule attachments and alert the spindle checkpoint to the presence of misaligned chromosomes. We show that Haspin inhibitors decreased H3T3ph, resulting in loss of centromeric Aurora B and reduced phosphorylation of centromere and kinetochore Aurora B substrates. Consequently, metaphase chromosome alignment and spindle checkpoint signaling were compromised. These effects were phenocopied by microinjection of anti-H3T3ph antibodies. Retargeting Aurora B to centromeres partially restored checkpoint signaling and Aurora B–dependent phosphorylation at centromeres and kinetochores, bypassing the need for Haspin activity. Haspin inhibitors did not obviously affect phosphorylation of histone H3 at serine-10 (H3S10ph) by Aurora B on chromosome arms but, in Aurora B reactivation assays, recovery of H3S10ph was delayed. Haspin inhibitors did not block Aurora B localization to the spindle midzone in anaphase or Aurora B function in cytokinesis. Thus, Haspin inhibitors reveal centromeric roles of Aurora B in chromosome movement and spindle checkpoint signaling.


Sign in / Sign up

Export Citation Format

Share Document