Evidence map›Paper›PMID 38851742›Full record

ArticleNature communications2024

Development of deaminase-free T-to-S base editor and C-to-G base editor by engineered human uracil DNA glycosylase.

Huawei Tong, Haoqiang Wang, Xuchen Wang, Nana Liu, Guoling Li, Danni Wu, Yun Li, Ming Jin, Hengbin Li, Yinghui Wei and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Base Editing: Mechanisms and Therapeutic Applications.Methods in molecular biology (Clifton, N.J.) · 2027
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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

16 authors.

Huawei Tong *HuidaGene Therapeutics Co., Ltd., Shanghai, China. tonghuawei@simm.ac.cn.ORCID http://orcid.org/0000-0002-9988-1818
Haoqiang Wang *HuidaGene Therapeutics Co., Ltd., Shanghai, China.ORCID http://orcid.org/0000-0003-4944-1117
Xuchen Wang *Institute of Neuroscience, State Key Laboratory of Neuroscience, Key Laboratory of Primate Neurobiology, Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.
Nana Liu *HuidaGene Therapeutics Co., Ltd., Shanghai, China.
Guoling LiHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Danni WuHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Yun LiHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Ming JinDepartment of Neurology and Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
Hengbin LiHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Yinghui WeiInternational Joint Agriculture Research Center for Animal Bio-Breeding of Ministry of Agriculture and Rural Affairs, College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, China.
Tong LiHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Yuan YuanHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Linyu ShiHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Xuan YaoHuidaGene Therapeutics Co., Ltd., Shanghai, China.
Yingsi ZhouHuidaGene Therapeutics Co., Ltd., Shanghai, China. yingsizhou@huidagene.com.ORCID http://orcid.org/0000-0002-6541-2116
Hui YangHuidaGene Therapeutics Co., Ltd., Shanghai, China. huiyang@huidagene.com.ORCID http://orcid.org/0000-0002-8023-0230

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA base editors enable direct editing of adenine (A), cytosine (C), or guanine (G), but there is no base editor for direct thymine (T) editing currently. Here we develop two deaminase-free glycosylase-based base editors for direct T editing (gTBE) and C editing (gCBE) by fusing Cas9 nickase (nCas9) with engineered human uracil DNA glycosylase (UNG) variants. By several rounds of structure-informed rational mutagenesis on UNG in cultured human cells, we obtain gTBE and gCBE with high activity of T-to-S (i.e., T-to-C or T-to-G) and C-to-G conversions, respectively. Furthermore, we conduct parallel comparison of gTBE/gCBE with those recently developed using other protein engineering strategies, and find gTBE/gCBE show the outperformance. Thus, we provide several base editors, gTBEs and gCBEs, with corresponding engineered UNG variants, broadening the targeting scope of base editors.

Indexed as

CRISPR-Associated Protein 9Gene EditingProtein EngineeringUracil-DNA GlycosidaseCRISPR-Cas SystemsCytosineDNAGuanineHEK293 CellsHumansMutagenesisThymineCRISPR-Associated Protein 9CytosineDNAGuanineThymineUracil-DNA Glycosidase

Identifiers

PMID38851742
PMCPMC11162499

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.