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大肠杆菌DNA腺嘌呤甲基转移酶(Dam)与非GATC序列结合的结构:对不依赖甲基化的转录抑制的潜在影响

Structures of Escherichia coli DNA adenine methyltransferase (Dam) in complex with a non-GATC sequence: potential implications for methylation-independent transcriptional repression.

作者信息

Horton John R, Zhang Xing, Blumenthal Robert M, Cheng Xiaodong

机构信息

Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.

Department of Medical Microbiology and Immunology and Program in Bioinformatics, The University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

出版信息

Nucleic Acids Res. 2015 Apr 30;43(8):4296-308. doi: 10.1093/nar/gkv251. Epub 2015 Apr 6.

Abstract

DNA adenine methyltransferase (Dam) is widespread and conserved among the γ-proteobacteria. Methylation of the Ade in GATC sequences regulates diverse bacterial cell functions, including gene expression, mismatch repair and chromosome replication. Dam also controls virulence in many pathogenic Gram-negative bacteria. An unexplained and perplexing observation about Escherichia coli Dam (EcoDam) is that there is no obvious relationship between the genes that are transcriptionally responsive to Dam and the promoter-proximal presence of GATC sequences. Here, we demonstrate that EcoDam interacts with a 5-base pair non-cognate sequence distinct from GATC. The crystal structure of a non-cognate complex allowed us to identify a DNA binding element, GTYTA/TARAC (where Y = C/T and R = A/G). This element immediately flanks GATC sites in some Dam-regulated promoters, including the Pap operon which specifies pyelonephritis-associated pili. In addition, Dam interacts with near-cognate GATC sequences (i.e. 3/4-site ATC and GAT). Taken together, these results imply that Dam, in addition to being responsible for GATC methylation, could also function as a methylation-independent transcriptional repressor.

摘要

DNA腺嘌呤甲基转移酶(Dam)在γ-变形菌中广泛存在且保守。GATC序列中腺嘌呤的甲基化调节多种细菌细胞功能,包括基因表达、错配修复和染色体复制。Dam还控制许多致病性革兰氏阴性菌的毒力。关于大肠杆菌Dam(EcoDam)有一个无法解释且令人困惑的现象,即转录上对Dam有反应的基因与启动子近端GATC序列的存在之间没有明显关系。在这里,我们证明EcoDam与一个不同于GATC的5碱基对非同源序列相互作用。非同源复合物的晶体结构使我们能够鉴定出一个DNA结合元件,GTYTA/TARAC(其中Y = C/T,R = A/G)。在一些受Dam调节的启动子中,包括指定肾盂肾炎相关菌毛的Pap操纵子,这个元件紧邻GATC位点。此外,Dam与近同源的GATC序列(即3/4位点的ATC和GAT)相互作用。综上所述,这些结果表明,Dam除了负责GATC甲基化外,还可能作为一种不依赖甲基化的转录抑制因子发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1bf/4417163/b095d9814d63/gkv251fig1.jpg

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