Evidence map›Paper›PMID 39041409›Full record

ArticleNucleic acids research2024

Structural analysis of the BisI family of modification dependent restriction endonucleases.

Katarzyna Szafran, Dominik Rafalski, Krzysztof Skowronek, Marek Wojciechowski, Asgar Abbas Kazrani, Mirosław Gilski, Shuang-Yong Xu, Matthias Bochtler

Abstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Katarzyna SzafranInternational Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0001-9517-692X
Dominik RafalskiInternational Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0002-3449-7460
Krzysztof SkowronekInternational Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0001-9973-7085
Marek WojciechowskiInternational Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0002-8935-3640
Asgar Abbas KazraniInternational Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0009-0008-2958-0025
Mirosław GilskiFaculty of Chemistry, Adam Mickiewicz University, Poznan.ORCID 0000-0002-3941-9947
Shuang-Yong XuNew England Biolabs, Ipswich, USA.ORCID 0000-0001-6293-8481
Matthias BochtlerInternational Institute of Molecular and Cell Biology, Warsaw, Poland.ORCID 0000-0001-7884-4463

Funding

Foundation for Polish Science POIR.04.04.00-00-5D81/17-0National Science Center 2018/30/Q/NZ2/00669Polish Agency for Academic Exchange PPI/APM/2018/1/00034
6 · The paper itself

Abstract

The BisI family of restriction endonucleases is unique in requiring multiple methylated or hydroxymethylated cytosine residues within a short recognition sequence (GCNGC), and in cleaving directly within this sequence, rather than at a distance. Here, we report that the number of modified cytosines that are required for cleavage can be tuned by the salt concentration. We present crystal structures of two members of the BisI family, NhoI and Eco15I_Ntd (N-terminal domain of Eco15I), in the absence of DNA and in specific complexes with tetra-methylated GCNGC target DNA. The structures show that NhoI and Eco15I_Ntd sense modified cytosine bases in the context of double-stranded DNA (dsDNA) without base flipping. In the co-crystal structures of NhoI and Eco15I_Ntd with DNA, the internal methyl groups (G5mCNGC) interact with the side chains of an (H/R)(V/I/T/M) di-amino acid motif near the C-terminus of the distal enzyme subunit and arginine residue from the proximal subunit. The external methyl groups (GCNG5mC) interact with the proximal enzyme subunit, mostly through main chain contacts. Surface plasmon resonance analysis for Eco15I_Ntd shows that the internal and external methyl binding pockets contribute about equally to sensing of cytosine methyl groups.

Indexed as

DNAModels, MolecularCatalytic DomainCrystallography, X-RayCytosineDeoxyribonucleases, Type II Site-SpecificDNA MethylationDNA Restriction EnzymesSubstrate SpecificityCytosineDeoxyribonucleases, Type II Site-SpecificDNADNA Restriction Enzymes

Identifiers

PMID39041409
PMCPMC11347163

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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.