Evidence map›Paper›PMID 30874552›Full record

ArticleNature communications2019

Lineage tracing using a Cas9-deaminase barcoding system targeting endogenous L1 elements.

Byungjin Hwang, Wookjae Lee, Soo-Young Yum, Yujin Jeon, Namjin Cho, Goo Jang, Duhee Bang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

41 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Genomic repeats for single-cell molecular recording.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Advances in CRISPR-Cas9 in lineage tracing of model animals.Animal models and experimental medicine · 2025
    Review
  13. Article
  14. Review
  15. The lives of cells, recorded.Nature reviews. Genetics · 2025
    Review
  16. Review
  17. Review
  18. Toward DNA-Based Recording of Biological Processes.International journal of molecular sciences · 2024
    Review
  19. Clonal tracking in cancer and metastasis.Cancer metastasis reviews · 2024
    Review
  20. Review
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

7 authors at 2 institutions in 2 countries.

Byungjin HwangDepartment of Chemistry, Yonsei University, Seoul, 03722, Korea.
Wookjae LeeDepartment of Chemistry, Yonsei University, Seoul, 03722, Korea.ORCID http://orcid.org/0000-0001-8891-9035
Soo-Young YumLaboratory of Theriogenology and Biotechnology, Department of Veterinary Clinical Sciences, College of Veterinary Medicine, the Research Institute of Veterinary Science, and BK21 PLUS Program for Creative Veterinary Science Research, Seoul National University, Seoul, 08826, Korea.ORCID http://orcid.org/0000-0002-9922-9168
Yujin JeonDepartment of Chemistry, Yonsei University, Seoul, 03722, Korea.ORCID http://orcid.org/0000-0002-0403-1360
Namjin ChoDepartment of Chemistry, Yonsei University, Seoul, 03722, Korea.
Goo JangLaboratory of Theriogenology and Biotechnology, Department of Veterinary Clinical Sciences, College of Veterinary Medicine, the Research Institute of Veterinary Science, and BK21 PLUS Program for Creative Veterinary Science Research, Seoul National University, Seoul, 08826, Korea. snujang@snu.ac.kr.ORCID http://orcid.org/0000-0003-3804-1871
Duhee BangDepartment of Chemistry, Yonsei University, Seoul, 03722, Korea. duheebang@yonsei.ac.kr.
Yonsei University · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Determining cell lineage and function is critical to understanding human physiology and pathology. Although advances in lineage tracing methods provide new insight into cell fate, defining cellular diversity at the mammalian level remains a challenge. Here, we develop a genome editing strategy using a cytidine deaminase fused with nickase Cas9 (nCas9) to specifically target endogenous interspersed repeat regions in mammalian cells. The resulting mutation patterns serve as a genetic barcode, which is induced by targeted mutagenesis with single-guide RNA (sgRNA), leveraging substitution events, and subsequent read out by a single primer pair. By analyzing interspersed mutation signatures, we show the accurate reconstruction of cell lineage using both bulk cell and single-cell data. We envision that our genetic barcode system will enable fine-resolution mapping of organismal development in healthy and diseased mammalian states.

Indexed as

Cell DifferentiationCell LineageCRISPR-Associated Protein 9Cytidine DeaminaseDNA Barcoding, TaxonomicGene EditingHEK293 CellsHeLa CellsHumansLong Interspersed Nucleotide ElementsMutagenesisRNA, Guide, CRISPR-Cas SystemsSingle-Cell AnalysisTime-Lapse ImagingCRISPR-Associated Protein 9Cytidine DeaminaseRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID30874552
PMCPMC6420643
OpenAlexW2949307008

What OpenQuestion 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 OpenQuestion graph.