scholarly journals Noninvasive Measurement of Interphase Chromatin Rheology In Vivo

2021 ◽  
Vol 120 (3) ◽  
pp. 318a
Author(s):  
Iraj Eshghi ◽  
Jonah Eaton ◽  
Alexandra Zidovska
1994 ◽  
Vol 59 (3) ◽  
pp. 309-313 ◽  
Author(s):  
David A. Russell ◽  
Roy H. Pottier ◽  
Dennis P. Valenzeno

2021 ◽  
Author(s):  
Veer I. P. Keizer ◽  
Simon Grosse-Holz ◽  
Maxime Woringer ◽  
Laura Zambon ◽  
Koceila Aizel ◽  
...  

AbstractOur understanding of the physical principles organizing the genome in the nucleus is limited by the lack of tools to directly exert and measure forces on interphase chromosomes in vivo and probe their material nature. Here, we present a novel approach to actively manipulate a genomic locus using controlled magnetic forces inside the nucleus of a living human cell. We observe viscoelastic displacements over microns within minutes in response to near-picoNewton forces, which are well captured by a Rouse polymer model. Our results highlight the fluidity of chromatin, with a moderate contribution of the surrounding material, revealing the minor role of crosslinks and topological effects and challenging the view that interphase chromatin is a gel-like material. Our new technology opens avenues for future research, from chromosome mechanics to genome functions.


2005 ◽  
Author(s):  
Olusola Soyemi ◽  
Michael Shear ◽  
Michelle Landry ◽  
Dulce Anunciacion ◽  
Babs Soller

2014 ◽  
Vol 255 (1) ◽  
pp. 42-48 ◽  
Author(s):  
N. AKBAR ◽  
S. SOKOLOVSKI ◽  
A. DUNAEV ◽  
J.J.F. BELCH ◽  
E. RAFAILOV ◽  
...  

1979 ◽  
Vol 81 (2) ◽  
pp. 453-457 ◽  
Author(s):  
J B Rattner ◽  
B A Hamkalo

Higher-order chromatin fibers (200--300 A in diameter) are reproducibly released from nuclei after lysis in the absence of formalin and/or detergent. Electron microscope analysis of these fibers shows that they are composed of a continuous array of closely apposed nucleosomes which display several distinct packing patterns. Analysis of the organization of nucleosomes within these arrays and their distribution along long stretches of chromatin suggest that the basic 100-A chromatin fiber is not packed into discrete superbeads and is not folded into a uniform solenoid within the native 250-A fiber. Furthermore, because similar higher-order fibers have been visualized in metaphase chromosomes, the existence of this fiber class appears to be independent of the degree of in vivo chromatin condensation.


1993 ◽  
Vol 106 (1) ◽  
pp. 189-199 ◽  
Author(s):  
P. Buchenau ◽  
D.J. Arndt-Jovin ◽  
H. Saumweber

The spatial distribution of no-on transient A (NONA), a protein associated with specific puffs on polytene chromosomes, was followed in nuclei of living Drosophila embryos by microinjection of fluorescently labeled monoclonal antibody to NONA. The injected antibodies remained active until the larval stage, revealing the distribution of the NONA protein throughout embryogenesis. Most injected animals completed embryonic development and hatched as normal larvae. NONA was restricted to the cytoplasm until the end of cycle 11. We document an active uptake of the NONA-antibody complex into early interphase nuclei from nuclear cycle 14 onwards, following each mitosis. Significant differences in the distribution of the protein between fixed and living embryos were apparent, particularly at high resolution. The NONA protein was localized in the nuclei of living embryos at discrete sites, most of which lay at the periphery and some of which were tightly clustered. The constellation of sites changed with time; in some nuclei these changes were fast whereas in other nuclei the pattern was quite stable. These data suggest that specific protein complexes associated with active interphase chromatin, and possibly chromatin in general, are mobile in the living organism.


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