scholarly journals Human female meiosis revised: new insights into the mechanisms of chromosome segregation and aneuploidies from advanced genomics and time-lapse imaging

2017 ◽  
Vol 23 (6) ◽  
pp. 706-722 ◽  
Author(s):  
Antonio Capalbo ◽  
Eva R Hoffmann ◽  
Danilo Cimadomo ◽  
Filippo Maria Ubaldi ◽  
Laura Rienzi
2015 ◽  
Vol 25 (15) ◽  
pp. R654-R656 ◽  
Author(s):  
Sarah E. Zanders ◽  
Harmit S. Malik

2020 ◽  
Vol 113 (5) ◽  
pp. 943-944
Author(s):  
Elpida Fragouli ◽  
Nicolas Garrido

2008 ◽  
Vol 105 (40) ◽  
pp. 15435-15440 ◽  
Author(s):  
Esteban Toro ◽  
Sun-Hae Hong ◽  
Harley H. McAdams ◽  
Lucy Shapiro

Chromosome segregation in bacteria is rapid and directed, but the mechanisms responsible for this movement are still unclear. We show thatCaulobacter crescentusmakes use of and requires a dedicated mechanism to initiate chromosome segregation.Caulobacterhas a single circular chromosome whose origin of replication is positioned at one cell pole. Upon initiation of replication, an 8-kb region of the chromosome containing both the origin andparSmoves rapidly to the opposite pole. This movement requires the highly conservedParABSlocus that is essential inCaulobacter.We use chromosomal inversions andin vivotime-lapse imaging to show thatparSis theCaulobactersite of force exertion, independent of its position in the chromosome. WhenparSis moved farther from the origin, the cell waits forparSto be replicated before segregation can begin. Also, a mutation in the ATPase domain of ParA halts segregation without affecting replication initiation. Chromosome segregation inCaulobactercannot occur unless a dedicatedparSguiding mechanism initiates movement.


2008 ◽  
Vol 24 (2) ◽  
pp. 86-93 ◽  
Author(s):  
Patricia A. Hunt ◽  
Terry J. Hassold

Cell ◽  
2017 ◽  
Vol 168 (6) ◽  
pp. 977-989.e17 ◽  
Author(s):  
Shunxin Wang ◽  
Terry Hassold ◽  
Patricia Hunt ◽  
Martin A. White ◽  
Denise Zickler ◽  
...  

2001 ◽  
Vol 92 (3-4) ◽  
pp. 342-344 ◽  
Author(s):  
F. Pardo-Manuel de Villena ◽  
C. Sapienza

2007 ◽  
Vol 18 (9) ◽  
pp. 3667-3680 ◽  
Author(s):  
James Edward Sillibourne ◽  
Bénédicte Delaval ◽  
Sambra Redick ◽  
Manisha Sinha ◽  
Stephen John Doxsey

Pericentrin is an integral centrosomal component that anchors regulatory and structural molecules to centrosomes. In a yeast two-hybrid screen with pericentrin we identified chromodomain helicase DNA-binding protein 4 (CHD4/Mi2β). CHD4 is part of the multiprotein nucleosome remodeling deacetylase (NuRD) complex. We show that many NuRD components interacted with pericentrin by coimmunoprecipitation and that they localized to centrosomes and midbodies. Overexpression of the pericentrin-binding domain of CHD4 or another family member (CHD3) dissociated pericentrin from centrosomes. Depletion of CHD3, but not CHD4, by RNA interference dissociated pericentrin and γ-tubulin from centrosomes. Microtubule nucleation/organization, cell morphology, and nuclear centration were disrupted in CHD3-depleted cells. Spindles were disorganized, the majority showing a prometaphase-like configuration. Time-lapse imaging revealed mitotic failure before chromosome segregation and cytokinesis failure. We conclude that pericentrin forms complexes with CHD3 and CHD4, but a distinct CHD3–pericentrin complex is required for centrosomal anchoring of pericentrin/γ-tubulin and for centrosome integrity.


Cell Cycle ◽  
2017 ◽  
Vol 16 (11) ◽  
pp. 1017-1019 ◽  
Author(s):  
Shunxin Wang ◽  
Nancy Kleckner ◽  
Liangran Zhang

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