TY - JOUR
T1 - Heterochromatin networks
T2 - Topology, dynamics, and function (a working hypothesis)
AU - Erenpreisa, Jekaterina
AU - Krigerts, Jekabs
AU - Salmina, Kristine
AU - Gerashchenko, Bogdan I.
AU - Freivalds, Talivaldis
AU - Kurg, Reet
AU - Winter, Ruth
AU - Krufczik, Matthias
AU - Zayakin, Pawel
AU - Hausmann, Michael
AU - Giuliani, Alessandro
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/7
Y1 - 2021/7
N2 - Open systems can only exist by self‐organization as pulsing structures exchanging matter and energy with the outer world. This review is an attempt to reveal the organizational principles of the heterochromatin supra‐intra‐chromosomal network in terms of nonlinear thermodynamics. The accessibility of the linear information of the genetic code is regulated by constitutive hetero-chromatin (CHR) creating the positional information in a system of coordinates. These features in-clude scale‐free splitting‐fusing of CHR with the boundary constraints of the nucleolus and nuclear envelope. The analysis of both the literature and our own data suggests a radial‐concentric network as the main structural organization principle of CHR regulating transcriptional pulsing. The dynamic CHR network is likely created together with nucleolus‐associated chromatin domains, while the alveoli of this network, including springy splicing speckles, are the pulsing transcription hubs. CHR contributes to this regulation due to the silencing position variegation effect, stickiness, and flexible rigidity determined by the positioning of nucleosomes. The whole system acts in concert with the elastic nuclear actomyosin network which also emerges by self‐organization during the transcriptional pulsing process. We hypothesize that the the transcriptional pulsing, in turn, adjusts its frequency/amplitudes specified by topologically associating domains to the replication timing code that determines epigenetic differentiation memory.
AB - Open systems can only exist by self‐organization as pulsing structures exchanging matter and energy with the outer world. This review is an attempt to reveal the organizational principles of the heterochromatin supra‐intra‐chromosomal network in terms of nonlinear thermodynamics. The accessibility of the linear information of the genetic code is regulated by constitutive hetero-chromatin (CHR) creating the positional information in a system of coordinates. These features in-clude scale‐free splitting‐fusing of CHR with the boundary constraints of the nucleolus and nuclear envelope. The analysis of both the literature and our own data suggests a radial‐concentric network as the main structural organization principle of CHR regulating transcriptional pulsing. The dynamic CHR network is likely created together with nucleolus‐associated chromatin domains, while the alveoli of this network, including springy splicing speckles, are the pulsing transcription hubs. CHR contributes to this regulation due to the silencing position variegation effect, stickiness, and flexible rigidity determined by the positioning of nucleosomes. The whole system acts in concert with the elastic nuclear actomyosin network which also emerges by self‐organization during the transcriptional pulsing process. We hypothesize that the the transcriptional pulsing, in turn, adjusts its frequency/amplitudes specified by topologically associating domains to the replication timing code that determines epigenetic differentiation memory.
KW - Chromatin organization
KW - Cytoskeleton
KW - Heterochromatin
KW - Networks
KW - Nucleolar boundary
KW - Physics of life
KW - Positional information
KW - Scale‐free oscillations
KW - Transcriptional pulsing
UR - https://www.scopus.com/pages/publications/85110321177
U2 - 10.3390/cells10071582
DO - 10.3390/cells10071582
M3 - Review article
C2 - 34201566
AN - SCOPUS:85110321177
SN - 2073-4409
VL - 10
JO - Cells
JF - Cells
IS - 7
M1 - 1582
ER -