Evidence map›Paper›PMID 27099293›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Noncanonical DNA-binding mode of repressor and its disassembly by antirepressor.

Minsik Kim, Hee Jung Kim, Sang Hyeon Son, Hye Jin Yoon, Youngbin Lim, Jong Woo Lee, Yeong-Jae Seok, Kyeong Sik Jin, Yeon Gyu Yu, Seong Keun Kim and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Characterization of a novel phage-plasmid vB_EcoM_ED targeting multidrug-resistant Escherichia coli isolates.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Minsik KimDepartment of Agricultural Biotechnology, Seoul National University, Seoul 08826, Korea; Center for Food Safety and Toxicology, Seoul National University, Seoul 08826, Korea;
Hee Jung KimDepartment of Bio and Nano Chemistry, Kookmin University, Seoul 02707, Korea;
Sang Hyeon SonDepartment of Bio and Nano Chemistry, Kookmin University, Seoul 02707, Korea;
Hye Jin YoonDepartment of Chemistry, College of Natural Sciences, Seoul National University, Seoul 08826, Korea;
Youngbin LimDepartment of Biophysics and Chemical Biology, Seoul National University, Seoul 08826, Korea;
Jong Woo LeeDepartment of Biophysics and Chemical Biology, Seoul National University, Seoul 08826, Korea;
Yeong-Jae SeokDepartment of Biophysics and Chemical Biology, Seoul National University, Seoul 08826, Korea; Department of Biological Sciences, Seoul National University, Seoul 08826, Korea; Institute of Microbiology, Seoul National University, Seoul 08826, Korea;
Kyeong Sik JinPohang Accelerator Laboratory, Pohang University of Science and Technology, Pohang, Kyungbuk 37673, Korea;
Yeon Gyu YuDepartment of Bio and Nano Chemistry, Kookmin University, Seoul 02707, Korea;
Seong Keun KimDepartment of Chemistry, College of Natural Sciences, Seoul National University, Seoul 08826, Korea; Department of Biophysics and Chemical Biology, Seoul National University, Seoul 08826, Korea;
Sangryeol RyuDepartment of Agricultural Biotechnology, Seoul National University, Seoul 08826, Korea; Center for Food Safety and Toxicology, Seoul National University, Seoul 08826, Korea; Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 08826, Korea; Center for Food and Bioconvergence, Seoul National University, Seoul 08826, Korea sangryu@snu.ac.kr hyungholee@snu.ac.kr.
Hyung Ho LeeDepartment of Chemistry, College of Natural Sciences, Seoul National University, Seoul 08826, Korea; sangryu@snu.ac.kr hyungholee@snu.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA-binding repressors are involved in transcriptional repression in many organisms. Disabling a repressor is a crucial step in activating expression of desired genes. Thus, several mechanisms have been identified for the removal of a stably bound repressor (Rep) from the operator. Here, we describe an uncharacterized mechanism of noncanonical DNA binding and induction by a Rep from the temperate Salmonella phage SPC32H; this mechanism was revealed using the crystal structures of homotetrameric Rep (92-198) and a hetero-octameric complex between the Rep and its antirepressor (Ant). The canonical method of inactivating a repressor is through the competitive binding of the antirepressor to the operator-binding site of the repressor; however, these studies revealed several noncanonical features. First, Ant does not compete for the DNA-binding region of Rep. Instead, the tetrameric Ant binds to the C-terminal domains of two asymmetric Rep dimers. Simultaneously, Ant facilitates the binding of the Rep N-terminal domains to Ant, resulting in the release of two Rep dimers from the bound DNA. Second, the dimer pairs of the N-terminal DNA-binding domains originate from different dimers of a Rep tetramer (trans model). This situation is different from that of other canonical Reps, in which two N-terminal DNA-binding domains from the same dimeric unit form a dimer upon DNA binding (cis model). On the basis of these observations, we propose a noncanonical model for the reversible inactivation of a Rep by an Ant.

Indexed as

Models, ChemicalModels, MolecularBacteriophagesBinding SitesComputer SimulationDNA, ViralNucleic Acid ConformationProtein BindingProtein ConformationRepressor ProteinsDNA, ViralRepressor ProteinsantirepressorbacteriophagerepressorSalmonellatranscription

Identifiers

PMID27099293
PMCPMC4983836

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.