scholarly journals Regulation of mitotic chromosome architecture and resolution of ultrafine anaphase bridges by PICH

Cell Cycle ◽  
2021 ◽  
pp. 1-14
Author(s):  
Primrose Chanboonyasitt ◽  
Ying Wai Chan
2019 ◽  
Vol 53 (1) ◽  
pp. 445-482 ◽  
Author(s):  
Stanislau Yatskevich ◽  
James Rhodes ◽  
Kim Nasmyth

Structural maintenance of chromosomes (SMC) complexes are key organizers of chromosome architecture in all kingdoms of life. Despite seemingly divergent functions, such as chromosome segregation, chromosome maintenance, sister chromatid cohesion, and mitotic chromosome compaction, it appears that these complexes function via highly conserved mechanisms and that they represent a novel class of DNA translocases.


2018 ◽  
Vol 217 (7) ◽  
pp. 2309-2328 ◽  
Author(s):  
Nike Walther ◽  
M. Julius Hossain ◽  
Antonio Z. Politi ◽  
Birgit Koch ◽  
Moritz Kueblbeck ◽  
...  

The two Condensin complexes in human cells are essential for mitotic chromosome structure. We used homozygous genome editing to fluorescently tag Condensin I and II subunits and mapped their absolute abundance, spacing, and dynamic localization during mitosis by fluorescence correlation spectroscopy (FSC)–calibrated live-cell imaging and superresolution microscopy. Although ∼35,000 Condensin II complexes are stably bound to chromosomes throughout mitosis, ∼195,000 Condensin I complexes dynamically bind in two steps: prometaphase and early anaphase. The two Condensins rarely colocalize at the chromatid axis, where Condensin II is centrally confined, but Condensin I reaches ∼50% of the chromatid diameter from its center. Based on our comprehensive quantitative data, we propose a three-step hierarchical loop model of mitotic chromosome compaction: Condensin II initially fixes loops of a maximum size of ∼450 kb at the chromatid axis, whose size is then reduced by Condensin I binding to ∼90 kb in prometaphase and ∼70 kb in anaphase, achieving maximum chromosome compaction upon sister chromatid segregation.


2016 ◽  
Vol 21 (10) ◽  
pp. 1113-1124 ◽  
Author(s):  
Masatoshi Takagi ◽  
Toyoaki Natsume ◽  
Masato T. Kanemaki ◽  
Naoko Imamoto

Cell ◽  
2003 ◽  
Vol 115 (1) ◽  
pp. 109-121 ◽  
Author(s):  
Takao Ono ◽  
Ana Losada ◽  
Michiko Hirano ◽  
Michael P. Myers ◽  
Andrew F. Neuwald ◽  
...  

2021 ◽  
Author(s):  
John Sedat ◽  
Angus McDonald ◽  
Herbert G Kasler ◽  
Eric Verdin ◽  
Hu Cang ◽  
...  

A molecular architecture is proposed for an example mitotic chromosome, human Chromosome 10. This architecture is built on a previously described interphase chromosome structure based on Cryo-EM cellular tomography (1), thus unifying chromosome structure throughout the complete mitotic cycle. The basic organizational principle, for mitotic chromosomes, is specific coiling of the 11-nm nucleosome fiber into large scale approximately 200 nm structures (a Slinky (2, motif cited in 3) in interphase, and then further modification and subsequent additional coiling for the final structure. The final mitotic chromosome architecture accounts for the dimensional values as well as the well known cytological configurations. In addition, proof is experimentally provided, by digital PCR technology, that G1 T-cell nuclei are diploid, thus one DNA molecule per chromosome. Many nucleosome linker DNA sequences, the promotors and enhancers, are suggestive of optimal exposure on the surfaces of the large-scale coils.


2018 ◽  
Author(s):  
Nike Walther ◽  
M. Julius Hossain ◽  
Antonio Z. Politi ◽  
Birgit Koch ◽  
Moritz Kueblbeck ◽  
...  

AbstractThe two Condensin complexes in human cells are essential for mitotic chromosome structure. We used homozygous genome editing to fluorescently tag Condensin I and II subunits and mapped their absolute abundance, spacing and dynamic localization during mitosis by fluorescence correlation spectroscopy-calibrated live cell imaging and super-resolution microscopy. While ∼35,000 Condensin II complexes are stably bound to chromosomes throughout mitosis, ∼195,000 Condensin I complexes dynamically bind in two steps, in prometaphase and early anaphase. The two Condensins rarely co-localize at the chromatid axis, where Condensin II is centrally confined but Condensin I reaches ∼50% of the chromatid diameter from its center. Based on our comprehensive quantitative data, we propose a three-step hierarchical loop model of mitotic chromosome compaction: Condensin II initially fixes loops of a maximum size of ∼450 kb at the chromatid axis whose size is then reduced by Condensin I binding to ∼90 kb in prometaphase and ∼70 kb in anaphase, achieving maximum chromosome compaction upon sister chromatid segregation.


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