Evidence map›Paper›PMID 41134629›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Single-cell metabolome and RNA-seq multiplexing on single plant cells.

Moonyoung Kang, Anh Hai Vu, Abbie L Casper, Rinho Kim, Jens Wurlitzer, Sarah Heinicke, Assa Yeroslaviz, Lorenzo Caputi, Sarah E O'Connor

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
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  8. Single-cell metabolome and RNA-seq multiplexing on single plant cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

9 authors.

Moonyoung Kang *Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.ORCID 0000-0002-4630-4312
Anh Hai Vu *Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.ORCID 0000-0002-7815-0426
Abbie L CasperNext Generation Sequencing and Bioinformatics Core Facility, Max Planck Institute for Biochemistry, München 82152, Germany.ORCID 0009-0005-4964-3087
Rinho KimNext Generation Sequencing and Bioinformatics Core Facility, Max Planck Institute for Biochemistry, München 82152, Germany.
Jens WurlitzerDepartment of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.
Sarah HeinickeDepartment of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.
Assa YeroslavizNext Generation Sequencing and Bioinformatics Core Facility, Max Planck Institute for Biochemistry, München 82152, Germany.ORCID 0000-0001-9638-4026
Lorenzo CaputiDepartment of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.ORCID 0000-0002-7783-6733
Sarah E O'ConnorDepartment of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.ORCID 0000-0003-0356-6213

Funding

Max Planck Society noneNational Research Foundation of Korea (NRF) RS-2023-00245281
6 · The paper itself

Abstract

Plants produce valuable natural products used for a wide variety of industrial applications. Thus, there is enormous interest in elucidating the biosynthetic pathways that are responsible for the production of these compounds. Identification of the genes that comprise these biosynthetic pathways has been enabled by gene-to-metabolite networks that are generated from transcriptomic and metabolomic datasets. Recent advances in both single-cell RNA-seq (scRNA-seq) and single-cell mass spectrometry metabolomics (scMS) have enabled the measurement of either gene expression or metabolite levels in individual cells. However, these datasets can only be used to indirectly correlate gene expression levels with metabolite concentrations at the single-cell level. In this proof-of-concept study, performed on cells derived from the leaves of the medicinal plant

Indexed as

CatharanthusMetabolomeMetabolomicsPlant CellsRNA-SeqSingle-Cell AnalysisGene Expression Regulation, PlantMass SpectrometryPlant LeavesProtoplastsSequence Analysis, RNATranscriptomeCatharanthus roseusplant natural productssingle-cell metabolomesingle-cell-omics multiplexingsingle-cell transcriptome

Identifiers

PMID41134629
PMCPMC12582292

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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.