Evidence map›Paper›PMID 40390480›Full record

ArticleJournal, genetic engineering & biotechnology2025

Uracil walking primer PCR: An accurate and efficient genome-walking tool.

Hong Chen, Bingkun Tian, Rongrong Wang, Zhenkang Pan, Dandan Gao, Haixing Li

Abstract read
In one paragraph

Article in Journal, genetic engineering & biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

6 authors.

Hong ChenState Key Laboratory of Food Science and Resource, Nanchang University, Nanchnag, China; International Institute of Food Innovation Co., Ltd., Nanchang University, Nanchnag, China; Sino-German Joint Research Institute, Nanchang University, Nanchang, China.
Bingkun TianState Key Laboratory of Food Science and Resource, Nanchang University, Nanchnag, China; International Institute of Food Innovation Co., Ltd., Nanchang University, Nanchnag, China; Sino-German Joint Research Institute, Nanchang University, Nanchang, China.
Rongrong WangState Key Laboratory of Food Science and Resource, Nanchang University, Nanchnag, China; International Institute of Food Innovation Co., Ltd., Nanchang University, Nanchnag, China; Sino-German Joint Research Institute, Nanchang University, Nanchang, China.
Zhenkang PanState Key Laboratory of Food Science and Resource, Nanchang University, Nanchnag, China; Sino-German Joint Research Institute, Nanchang University, Nanchang, China.
Dandan GaoCollege of Life Sciences and Engineering, Northwest Minzu University, Lanzhou, China. Electronic address: gaodan0322@163.com.
Haixing LiState Key Laboratory of Food Science and Resource, Nanchang University, Nanchnag, China; International Institute of Food Innovation Co., Ltd., Nanchang University, Nanchnag, China; Sino-German Joint Research Institute, Nanchang University, Nanchang, China. Electronic address: hxli@ncu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome walking PCR has been extensively used to acquire unknown genomic regions bordering known DNAs. However, non-target amplification challenges the efficacy of existing genome-walking PCRs. Herein, we conceived a new genome-walking method termed Uracil walking Primer PCR (UP-PCR). The UP-PCR features introducing an uracil base at the penultimate position of arbitrary walking primer (AWP) 3' end. A UP-PCR set comprises three nested amplification steps, which are performed by an AWP sequentially coupling a set of three nested site-specific primers, respectively. Prior to secondary UP-PCR, primary UP-PCR product is processed with uracil DNA glycosylase to destroy the carried AWP. As a result, only target primary product is exponentially amplified in the next UP-PCR(s), as it is the only product with binding sites for the both primers. The performance of UP-PCR has been validated by walking three selected genes. The walking experiments showed that each secondary or tertiary UP-PCR generated one to two amplicon ranging in size from 0.2 to 5.0 kb, while with a negligible non-target background; and the amplicons of the secondary UP-PCRs were all correct, indicating that tertiary UP-PCR is generally unnecessary. These findings suggested that UP-PCR has a satisfactory walking ability, specificity, and speed. Collectively, the proposed UP-PCR is a potential candidate method for genome walking.

Indexed as

Genome walkingnested PCRRandomly partial annealingUracil DNA glycosylaseUracil walking primer

Identifiers

PMID40390480
PMCPMC11957515

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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.