Evidence map›Paper›PMID 41298979›Full record

ArticleCommunications biology2025

A programmable pAgo nuclease with high activity and specificity for efficient DNA and RNA manipulation.

Jiao Hu, Yangyang Hu, Yang Wang, Hengrong Jiang, Meng Chen, Jingjing Zhang, Fajun Lai, Xiu Li, Yibin Cheng, Tao Liu and 4 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

14 authors.

Jiao Hu *State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Yangyang Hu *State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Yang Wang *State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Hengrong JiangState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Meng ChenState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Jingjing ZhangState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Fajun LaiState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Xiu LiState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Yibin ChengState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Tao LiuState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.ORCID http://orcid.org/0000-0001-8094-2572
Guoli YangState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China.
Fei WangState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China. wangfei@hubu.edu.cn.ORCID http://orcid.org/0000-0003-1133-2505
Wenqiang LiState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China. li-wenqiang@hubu.edu.cn.ORCID http://orcid.org/0000-0002-3951-6691
Lixin MaState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative, Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial. Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, China. malixing@hubu.edu.cn.ORCID http://orcid.org/0000-0002-2016-9781

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prokaryotic Argonaute proteins (pAgos) are programmable nucleases with potential for the development of novel nucleic acid manipulation tools. Previous studies have shown that several pAgos exhibit strong preferences for either DNA or RNA targets, and effective cleavage of plasmid or linear double-stranded DNA (dsDNA) is typically limited to regions with low GC content. Here, we characterize a pAgo, GgeAgo from the thermophilic organism Geobacillus genomosp. 3. GgeAgo utilizes 5' phosphorylated DNA guides to cleave both DNA and RNA with high efficiency and specificity under a wide range of conditions. Notably, GgeAgo efficiently cleaves both plasmid and linear dsDNA with GC content up to 53% at elevated temperatures, and retains detectable activity even at 64% GC. Furthermore, GgeAgo demonstrates robust activity in practical applications, including DNA cloning, nucleic acid detection, and enrichment of rare variants, with high specificity and sensitivity. These results suggest that GgeAgo holds promise as an effective DNA and RNA manipulation tool for biotechnology.

Indexed as

Argonaute ProteinsBacterial ProteinsDNAGeobacillusRNAPlasmidsSubstrate SpecificityArgonaute ProteinsBacterial ProteinsDNARNA

Identifiers

PMID41298979
PMCPMC12657969

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.