5-Formyluracil targeted biochemical reactions with proteins inhibit DNA replication, induce mutations and interference gene expression in living cells
5-Formyluracil targeted biochemical reactions with proteins inhibit DNA replication, induce mutations and interference gene expression in living cells
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5-甲酰尿嘧啶与蛋白质发生靶向生化反应,抑制活细胞中的 DNA 复制、诱导突变并干扰基因表达
DOI:
10.1016/j.cclet.2021.02.036
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发表时间:
2021-02
影响因子:
9.1
通讯作者:
Zhou Xiang
中科院分区:
文献类型:
--
作者:
Zou Guangrong;Zhang Kaiyuan;Yang Wei;Liu Chaoxing;Fang Zhentian;Zhou Xiang
Covalent DNA–protein cross-links are toxic DNA lesions that interfere with essential biological processes, which can cause serious biological consequences, such as genomic instability and protein misexpression. 5-Formyluracil (5fU) as an important modification in DNA, which is mainly from oxidative damage, exists in a variety of cells and tissues. We have reported that 5fU mediated DNA–protein conjugates could exist in human cells [Zhouet al. CCS Chem. 2 (2020) 54–63]. We now aimed to explore its potential biological effectsin vitroandin vivo. In this paper, we firstly reported that 5fU intermediated DNA–peptide or DNA–protein conjugates (both were called DPCs) could inhibit different polymerases bypass or cause mutations. Then we further investigated the functional impacts caused by 5fU-mediated DPCs, which appeared in different gene expression components [in the promoter sequence or 5′-untranslated regions (UTR)]. These results together may contribute to a broader understanding of DNA–protein interactions as well as the biological functions associated with 5fU.
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影响因子:
4.1
作者:
Pande P;Ji S;Mukherjee S;Schärer OD;Tretyakova NY;Basu AK
通讯作者:
Basu AK
影响因子:
15
作者:
Hardisty RE;Kawasaki F;Sahakyan AB;Balasubramanian S
通讯作者:
Balasubramanian S
影响因子:
4.1
作者:
Sanchez, AM;Minko, IG;Lloyd, RS
通讯作者:
Lloyd, RS
DOI:
10.1002/anie.201708286
发表时间:
2017-11-06
期刊:
Angewandte Chemie (International ed. in English)
影响因子:
--
作者:
Ji S;Shao H;Han Q;Seiler CL;Tretyakova NY
通讯作者:
Tretyakova NY
影响因子:
18.3
作者:
Tretyakova NY;Groehler A 4th;Ji S
通讯作者:
Ji S