Evidence map›Paper›PMID 30873540›Full record

ArticleNucleic acids research2019

Single-cell transcriptome analysis of Physcomitrella leaf cells during reprogramming using microcapillary manipulation.

Minoru Kubo, Tomoaki Nishiyama, Yosuke Tamada, Ryosuke Sano, Masaki Ishikawa, Takashi Murata, Akihiro Imai, Daniel Lang, Taku Demura, Ralf Reski and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 51 citations in OpenAlex.

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  10. Single-cell technologies: From research to application.Innovation (Cambridge (Mass.)) · 2022
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  20. The promise of single-cell genomics in plants.Current opinion in plant biology · 2020
    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

11 authors at 5 institutions in 2 countries.

Minoru KuboInstitute for Research Initiative, Nara Institute of Science and Technology, Ikoma 630-0192, Japan.
Tomoaki NishiyamaAdvanced Science Research Center, Kanazawa University, Kanazawa 920-0934, Japan.
Yosuke TamadaNational Institute for Basic Biology, Okazaki 444-8585, Japan.
Ryosuke SanoGraduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma 630-0192, Japan.
Masaki IshikawaNational Institute for Basic Biology, Okazaki 444-8585, Japan.
Takashi MurataNational Institute for Basic Biology, Okazaki 444-8585, Japan.
Akihiro ImaiFaculty of Life Sciences, Hiroshima Institute of Technology, Hiroshima 731-5193, Japan.
Daniel LangPlant Biotechnology, Faculty of Biology, University of Freiburg, 79104 Freiburg, Germany.
Taku DemuraGraduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma 630-0192, Japan.
Ralf ReskiPlant Biotechnology, Faculty of Biology, University of Freiburg, 79104 Freiburg, Germany.
Mitsuyasu HasebeNational Institute for Basic Biology, Okazaki 444-8585, Japan.
National Institute for Basic Biology · JPNara Institute of Science and Technology · JPUniversity of Freiburg · DEHiroshima Institute of Technology · JPKanazawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next-generation sequencing technologies have made it possible to carry out transcriptome analysis at the single-cell level. Single-cell RNA-sequencing (scRNA-seq) data provide insights into cellular dynamics, including intercellular heterogeneity as well as inter- and intra-cellular fluctuations in gene expression that cannot be studied using populations of cells. The utilization of scRNA-seq is, however, restricted to cell types that can be isolated from their original tissues, and it can be difficult to obtain precise positional information for these cells in situ. Here, we established single cell-digital gene expression (1cell-DGE), a method of scRNA-seq that uses micromanipulation to extract the contents of individual living cells in intact tissue while recording their positional information. With 1cell-DGE, we could detect differentially expressed genes (DEGs) during the reprogramming of leaf cells of the moss Physcomitrella patens, identifying 6382 DEGs between cells at 0 and 24 h after excision. Furthermore, we identified a subpopulation of reprogramming cells based on their pseudotimes, which were calculated using transcriptome profiles at 24 h. 1cell-DGE with microcapillary manipulation can be used to analyze the gene expression of individual cells without detaching them from their tightly associated tissues, enabling us to retain positional information and investigate cell-cell interactions.

Indexed as

BryopsidaCellular ReprogrammingGene Expression ProfilingPlant LeavesSequence Analysis, RNASingle-Cell AnalysisSoftwareTranscriptome

Identifiers

PMID30873540
PMCPMC6511839
OpenAlexW2952987309

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.