scholarly journals Higher-order structure of DNA determines its positioning in cell-size droplets under crowded conditions

PLoS ONE ◽  
2021 ◽  
Vol 16 (12) ◽  
pp. e0261736
Author(s):  
Takashi Nishio ◽  
Yuko Yoshikawa ◽  
Kenichi Yoshikawa

Background It is becoming clearer that living cells use water/water (w/w) phase separation to form membraneless organelles that exhibit various important biological functions. Currently, it is believed that the specific localization of biomacromolecules, including DNA, RNA and proteins in w/w microdroplets is closely related to their bio-activity. Despite the importance of this possible role of micro segregation, our understanding of the underlying physico-chemical mechanism is still unrefined. Further research to unveil the underlying mechanism of the localization of macromolecules in relation to their steric conformation in w/w microdroplets is needed. Principal findings Single-DNA observation of genome-size DNA (T4 GT7 bacteriophage DNA; 166kbp) by fluorescence microscopy revealed that DNAs are spontaneously incorporated into w/w microdroplets generated in a binary aqueous polymer solution with polyethylene glycol (PEG) and dextran (DEX). Interestingly, DNAs with elongated coil and shrunken conformations exhibit Brownian fluctuation inside the droplet. On the other hand, tightly packed compact globules, as well as assemblies of multiple condensed DNAs, tend to be located near the interface in the droplet. Conclusion and significance The specific localization of DNA molecules depending on their higher-order structure occurs in w/w microdroplet phase-separation solution under a binary aqueous polymer solution. Such an aqueous solution with polymers mimics the crowded conditions in living cells, where aqueous macromolecules exist at a level of 30–40 weight %. The specific positioning of DNA depending on its higher-order structure in w/w microdroplets is expected to provide novel insights into the mechanism and function of membraneless organelles and micro-segregated particles in living cells.

2003 ◽  
Vol 29 (1) ◽  
pp. 144-146 ◽  
Author(s):  
Hironobu Imakoma ◽  
Ryo Omori ◽  
Katsuyuki Kubota ◽  
Masamichi Yoshida

2002 ◽  
Vol 28 (4) ◽  
pp. 488-489 ◽  
Author(s):  
Hironobu Imakoma ◽  
Tatsuhiro Nakazawa ◽  
Katsuyuki Kubota ◽  
Masamichi Yoshida

2003 ◽  
Vol 29 (5) ◽  
pp. 695-697 ◽  
Author(s):  
Hironobu Imakoma ◽  
Takeshi Mori ◽  
Katsuyuki Kubota ◽  
Masamichi Yoshida

2006 ◽  
Vol 26 (1) ◽  
pp. 155-168 ◽  
Author(s):  
Jizhou Yan ◽  
Lisha Xu ◽  
Gregory Crawford ◽  
Zenfeng Wang ◽  
Shawn M. Burgess

ABSTRACT All forkhead (Fox) proteins contain a highly conserved DNA binding domain whose structure is remarkably similar to the winged-helix structures of histones H1 and H5. Little is known about Fox protein binding in the context of higher-order chromatin structure in living cells. We created a stable cell line expressing FoxI1-green fluorescent protein (GFP) or FoxI1-V5 fusion proteins under control of the reverse tetracycline-controlled transactivator doxycycline inducible system and found that unlike most transcription factors, FoxI1 remains bound to the condensed chromosomes during mitosis. To isolate DNA fragments directly bound by the FoxI1 protein within living cells, we performed chromatin immunoprecipitation assays (ChIPs) with antibodies to either enhanced GFP or the V5 epitope and subcloned the FoxI1-enriched DNA fragments. Sequence analyses indicated that 88% (106/121) of ChIP sequences contain the consensus binding sites for all Fox proteins. Testing ChIP sequences with a quantitative DNase I hypersensitivity assay showed that FoxI1 created stable DNase I sensitivity changes in condensed chromosomes. The majority of ChIP targets and random targets increased in resistance to DNase I in FoxI1-expressing cells, but a small number of targets became more accessible to DNase I. Consistently, the accessibility of micrococcal nuclease to chromatin was generally inhibited. Micrococcal nuclease partial digestion generated a ladder in which all oligonucleosomes were slightly longer than those observed with the controls. On the basis of these findings, we propose that FoxI1 is capable of remodeling chromatin higher-order structure and can stably create site-specific changes in chromatin to either stably create or remove DNase I hypersensitive sites.


1992 ◽  
Vol 97 (11) ◽  
pp. 8722-8726 ◽  
Author(s):  
Nobuhiro Miura ◽  
Naoki Shinyashiki ◽  
Satoru Mashimo

Author(s):  
V.V. Pukhnachev ◽  
A.G. Petrova ◽  
O.A. Frolovskaya

Mathematical models for the motion of weak solutions of polymers have been studied over the past 50 years. The initial model (Voitkunskii, Amfilokhiev, and Pavlovskii, 1970) contains two key parameters - relaxation viscosity and shear stress relaxation time. In the limiting case, when the last parameter is small, the Pavlovskii model (1971) arises. Its equations are close to second-grade fluid equations (Rivlin and Eriksen, 1955). The paper contains an overview of the works on all three models and new results related to the Pavlovskii model. The solution to the problem of the un-steady layered flow of an aqueous polymer solution in a layer with a free boundary, the boundary condition on which includes the time derivative of the desired function is constructed. We derive the equations that describe the motion of a polymer solution in a laminar boundary layer near a rectilinear plate. The parameter included in equations characterizes the ratio of the thickness of the Prandtl boundary layer to the thickness of the relaxation boundary layer. We study the influence of this parameter on the motion picture by the example of a stationary flow near a critical point.


2019 ◽  
Vol 2019.56 (0) ◽  
pp. E014
Author(s):  
Yu NORIMATSU ◽  
Raden R. SISWORO ◽  
Masato HASEGAWA

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