Evidence map›Paper›PMID 36064973›Full record

ArticleNature chemistry2022

A modular XNAzyme cleaves long, structured RNAs under physiological conditions and enables allele-specific gene silencing.

Alexander I Taylor, Christopher J K Wan, Maria J Donde, Sew-Yeu Peak-Chew, Philipp Holliger

Abstract read
In one paragraph

Article in Nature chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  20. DNAzyme-Catalyzed Site-Specific N-Acylation of DNA Oligonucleotide Nucleobases.Angewandte Chemie (International ed. in English) · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Alexander I TaylorCambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), University of Cambridge, Cambridge, UK. ait29@cam.ac.uk.ORCID 0000-0001-7684-1437
Christopher J K WanMRC Laboratory of Molecular Biology, Cambridge, UK.
Maria J DondeCambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), University of Cambridge, Cambridge, UK.ORCID 0000-0003-4216-4719
Sew-Yeu Peak-ChewMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0002-7602-6384
Philipp HolligerMRC Laboratory of Molecular Biology, Cambridge, UK. ph1@mrc-lmb.cam.ac.uk.ORCID 0000-0002-3440-9854

Funding

Biotechnology and Biological Sciences Research Council BB/M005623/1Medical Research Council MC_U105178804Medical Research Council MC_U105184326Wellcome Trust 215453
6 · The paper itself

Abstract

Nucleic-acid catalysts (ribozymes, DNA- and XNAzymes) cleave target (m)RNAs with high specificity but have shown limited efficacy in clinical applications. Here we report on the in vitro evolution and engineering of a highly specific modular RNA endonuclease XNAzyme, FR6_1, composed of 2'-deoxy-2'-fluoro-β-D-arabino nucleic acid (FANA). FR6_1 overcomes the activity limitations of previous DNA- and XNAzymes and can be retargeted to cleave highly structured full-length (>5 kb) BRAF and KRAS mRNAs at physiological Mg

Indexed as

Nucleic AcidsProto-Oncogene Proteins B-rafAllelesGene SilencingHumansProto-Oncogene Proteins p21(ras)RNANucleic AcidsProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)RNA

Identifiers

PMID36064973
PMCPMC7613789

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Registered trials

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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.