Evidence map›Paper›PMID 28580104›Full record

ArticleChemical science2017

Highly specific imaging of mRNA in single cells by target RNA-initiated rolling circle amplification.

Ruijie Deng, Kaixiang Zhang, Yupeng Sun, Xiaojun Ren, Jinghong Li

Abstract read
In one paragraph

Article in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Mapping Embryonic Mouse Lung Development Using Enhanced Spatial Transcriptomics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Applications and development of in situ nucleic acid visualization techniques.Frontiers in bioengineering and biotechnology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Multiplexed in situ RNA imaging by combFISH.Analytical and bioanalytical chemistry · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

5 authors.

Ruijie DengDepartment of Chemistry , Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology , Beijing Key Laboratory for Microanalytical Methods and Instrumentation , Tsinghua University , Beijing 100084 , China . Email: jhli@mail.tsinghua.edu.cn.
Kaixiang ZhangDepartment of Chemistry , Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology , Beijing Key Laboratory for Microanalytical Methods and Instrumentation , Tsinghua University , Beijing 100084 , China . Email: jhli@mail.tsinghua.edu.cn.
Yupeng SunDepartment of Chemistry , Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology , Beijing Key Laboratory for Microanalytical Methods and Instrumentation , Tsinghua University , Beijing 100084 , China . Email: jhli@mail.tsinghua.edu.cn.
Xiaojun RenDepartment of Chemistry , Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology , Beijing Key Laboratory for Microanalytical Methods and Instrumentation , Tsinghua University , Beijing 100084 , China . Email: jhli@mail.tsinghua.edu.cn.
Jinghong LiDepartment of Chemistry , Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology , Beijing Key Laboratory for Microanalytical Methods and Instrumentation , Tsinghua University , Beijing 100084 , China . Email: jhli@mail.tsinghua.edu.cn.ORCID 0000-0002-0750-7352

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detection of single-cell gene expression with high spatial and sequence resolution is a key challenge in single cell biology. Herein, we propose a robust method for the direct detection of mRNA, termed target RNA-initiated rolling circle amplification, which enables imaging of mRNA with single-nucleotide and near-single-molecule resolution in single cells. By utilizing a Splint R ligase capable of efficiently catalyzing the ligation of a padlock probe by the target RNA, the method can enable the efficient detection of mRNA without reverse transcription (detection efficiency over 20%). Meanwhile, attributed to the ligation-based recognition process, the method confers specificity sufficient to genotype mRNAs with one-nucleotide variations. The method has enabled the spatial mapping and correlation analysis of gene expression in single cells which could help us to elucidate the gene functions and regulatory mechanisms. This method offers an mRNA profiling ability with high spatial resolution and sequence specificity, thus is expected to be a single-cell analysis platform for not only investigating gene expression, but also potentially for analyzing single-nucleotide variants or mRNA alternative splicing at single-cell level.

Identifiers

PMID28580104
PMCPMC5437493

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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.