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Comparative analysis of epigenetic inhibitors reveals different degrees of interference with transcriptional gene silencing and induction of DNA damage.

Comparative analysis of epigenetic inhibitors reveals different degrees of interference with transcriptional gene silencing and induction of DNA damage.

Authors :
Nowicka A
Tokarz B
Zwyrtková J
Dvořák Tomaštíková E
Procházková K
Ercan U
Finke A
Rozhon W
Poppenberger B
Otmar M
Niezgodzki I
Krečmerová M
Schubert I
Pecinka A
Source :
The Plant journal : for cell and molecular biology [Plant J] 2020 Apr; Vol. 102 (1), pp. 68-84. Date of Electronic Publication: 2019 Dec 12.
Publication Year :
2020

Abstract

Repetitive DNA sequences and some genes are epigenetically repressed by transcriptional gene silencing (TGS). When genetic mutants are not available or problematic to use, TGS can be suppressed by chemical inhibitors. However, informed use of epigenetic inhibitors is partially hampered by the absence of any systematic comparison. In addition, there is emerging evidence that epigenetic inhibitors cause genomic instability, but the nature of this damage and its repair remain unclear. To bridge these gaps, we compared the effects of 5-azacytidine (AC), 2'-deoxy-5-azacytidine (DAC), zebularine and 3-deazaneplanocin A (DZNep) on TGS and DNA damage repair. The most effective inhibitor of TGS was DAC, followed by DZNep, zebularine and AC. We confirmed that all inhibitors induce DNA damage and suggest that this damage is repaired by multiple pathways with a critical role of homologous recombination and of the SMC5/6 complex. A strong positive link between the degree of cytidine analog-induced DNA demethylation and the amount of DNA damage suggests that DNA damage is an integral part of cytidine analog-induced DNA demethylation. This helps us to understand the function of DNA methylation in plants and opens the possibility of using epigenetic inhibitors in biotechnology.<br /> (© 2019 The Authors. The Plant Journal © 2019 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-313X
Volume :
102
Issue :
1
Database :
MEDLINE
Journal :
The Plant journal : for cell and molecular biology
Publication Type :
Academic Journal
Accession number :
31733119
Full Text :
https://doi.org/10.1111/tpj.14612