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. 2020 Dec 3;10:21146. doi: 10.1038/s41598-020-78302-5

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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tdh2 gene deletion can suppress the DNA damage sensitivity of hst3∆ hst4∆ cells. (a,c) Plate assays monitoring the sensitivity of each DNA damaging agent (methyl methanesulfonate (MMS), hydroxyurea (HU) and camptothecin (CPT)). A ten-fold dilution of the cell suspension was sequentially diluted (from left to right) and then spotted on solid medium. WT: wild-type. (b) Rad53 phosphorylation was detected by western blotting using an anti-Rad53 antibody. Ponceau S staining indicates the total amount of protein on the membrane. (d) Acetylation level of histone H3-K56 on G2/M phase-arrested cells.