scholarly journals Exploring Secrets of Nuclear Actin Involvement in the Regulation of Gene Transcription and Genome Organization

Author(s):  
Yong Zhong ◽  
Cynthia Kanagaratham ◽  
Danuta Radzioch

2020 ◽  
Vol 102 ◽  
pp. 105-112 ◽  
Author(s):  
Salla Kyheröinen ◽  
Maria K. Vartiainen


2007 ◽  
Vol 102 (2) ◽  
pp. 403-411 ◽  
Author(s):  
Zhaoxia Song ◽  
Min Wang ◽  
Xiaoguang Wang ◽  
Xuefang Pan ◽  
Wenguang Liu ◽  
...  


2021 ◽  
Author(s):  
Gang Cao ◽  
Da Lin ◽  
Weize Xu ◽  
Ping Hong ◽  
Chengchao Wu ◽  
...  

Abstract The highly organized three-dimensional genome is crucial for gene transcription. However, it remains elusive how the order of the genome architecture related to its function. Here, we developed a single-cell Hi-C method and proposed TAD “degree of disorder” as a measure of genome organizational patterns, which is correlated with the chromatin epigenetic states, gene expression and co-regulation, and chromatin structure variability in individual cells. Upon Mycobacterium tuberculosis infection, NF-κB enters into the nucleus, binds to the target genome regions and initiates systematic chromatin conformation reorganization. Furthermore, we identified a remote NF-κB enriched enhancer promotes the expression of PD-L1 through chromatin loop, which could be a potential anti-tuberculosis and even anti-tumor therapeutic target. The integrated Hi-C, eQTL, and GWAS analysis depicted the atlas of the long-range target genes of tuberculosis susceptible loci. Among which SNP rs1873613 is located in the anchor of a dynamic chromatin loop with LRRK2, whose inhibitor AdoCbl could be an anti-tuberculosis drug candidate. Our study provides comprehensive resources for the 4D genome of immunocytes and sheds insights into the genome organization order and the coordinated gene transcription.





Traffic ◽  
2005 ◽  
Vol 6 (10) ◽  
pp. 847-857 ◽  
Author(s):  
Jan Gettemans ◽  
Katrien Van Impe ◽  
Veerle Delanote ◽  
Thomas Hubert ◽  
Joël Vandekerckhove ◽  
...  


2005 ◽  
Vol 16 (11) ◽  
pp. 5055-5060 ◽  
Author(s):  
Thoru Pederson ◽  
Ueli Aebi

Within the past two years, actin has been implicated in eukaryotic gene transcription by all three classes of RNA polymerase. Moreover, within just the past year, actin has been identified as a constituent of filaments attached to the nuclear pore complexes and extending into the nucleus. This review summarizes these and other very recent advances in the nuclear actin field and emphasizes the key present issues. On the one hand, we are confronted with a body of evidence for a role of actin in gene transcription but with no known structural basis; on the other hand, there is now evidence for polymeric actin—not likely in the classical F-actin conformation—in the nuclear periphery with no known function. In addition, numerous proteins that interact with either G- or F-actin are increasingly being detected in the nucleus, suggesting that both monomeric and oligomeric or polymeric forms of actin are at play and raising the possibility that the equilibrium between them, perhaps differentially regulated at various intranuclear sites, may be a major determinant of nuclear function.



2009 ◽  
Vol 29 (14) ◽  
pp. 4512-4518 ◽  
Author(s):  
S. Stern ◽  
E. Debre ◽  
C. Stritt ◽  
J. Berger ◽  
G. Posern ◽  
...  


2020 ◽  
Author(s):  
Christine R. Keenan ◽  
Hannah D. Coughlan ◽  
Nadia Iannarella ◽  
Timothy M. Johanson ◽  
Wing Fuk Chan ◽  
...  

SummaryH3K9me3-dependent heterochromatin is critical for the silencing of repeat-rich pericentromeric regions and also has key roles in repressing lineage-inappropriate protein-coding genes in differentiation and development. Here, we investigate the molecular consequences of heterochromatin loss in cells deficient in both Suv39h1 and Suv39h2 (Suv39DKO), the major mammalian histone methyltransferase enzymes that catalyse heterochromatic H3K9me3 deposition. Unexpectedly, we reveal a predominant repression of protein-coding genes in Suv39DKO cells, with these differentially expressed genes principally in euchromatic (DNaseI-accessible, H3K27ac-marked) rather than heterochromatic (H3K9me3-marked) regions. Examination of the 3D nucleome reveals that transcriptomic dysregulation occurs in euchromatic regions close to the nuclear periphery in 3-dimensional space. Moreover, this transcriptomic dysregulation is highly correlated with altered 3-dimensional genome organization in Suv39DKO cells. Together, our results suggest that the nuclear lamina-tethering of Suv39-dependent H3K9me3 domains provides an essential scaffold to support euchromatic genome organisation and the maintenance of gene transcription for healthy cellular function.



2001 ◽  
Vol 268 (6) ◽  
pp. 1802-1810
Author(s):  
Danielle Naville ◽  
Estelle Bordet ◽  
Marie-Claude Berthelon ◽  
Philippe Durand ◽  
Martine Begeot


2001 ◽  
Vol 61 (7) ◽  
pp. 61-67 ◽  
Author(s):  
Thomas V. O. Hansen ◽  
Finn C. Nielsen
Keyword(s):  


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