Evidence map›Paper›PMID 25575081›Full record

ArticleCell stem cell2015

Single-cell transcriptome analysis reveals dynamic changes in lncRNA expression during reprogramming.

Daniel H Kim, Georgi K Marinov, Shirley Pepke, Zakary S Singer, Peng He, Brian Williams, Gary P Schroth, Michael B Elowitz, Barbara J Wold

Abstract read
In one paragraph

Article in Cell stem cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
8.4field-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

99 citing papers in PubMed, 166 citations in OpenAlex.

  1. The Regulatory Potential of Long Non-Coding RNAs in Bipolar Disorder.International journal of molecular sciences · 2026
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  20. Detecting Cell Compartment-Specific PRC2-RNA Interactions via UV-RIP.Methods in molecular biology (Clifton, N.J.) · 2023
    Article

39 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Daniel H KimDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: dkim@caltech.edu.
Georgi K MarinovDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Shirley PepkeCenter for Advanced Computing Research, California Institute of Technology, Pasadena, CA 91125, USA.
Zakary S SingerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Howard Hughes Medical Institute, California Institute of Technology, Pasadena, CA 91125, USA.
Peng HeDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Brian WilliamsDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Gary P SchrothIllumina, Incorporated, San Diego, CA 92122, USA.
Michael B ElowitzDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Howard Hughes Medical Institute, California Institute of Technology, Pasadena, CA 91125, USA.
Barbara J WoldDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: woldb@caltech.edu.
California Institute of Technology · USHoward Hughes Medical Institute · USIllumina (United States) · US

Funding

Toward a comprehensive functional annotation of the human genomeU54HG006998 · NHGRI · HUDSON-ALPHA INSTITUTE FOR BIOTECHNOLOGY · PI MYERS, RICHARD M · 2012 to 2016
$17.5M
Training SubprojectU54HG007990 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI HAUSSLER, DAVID H, PATTERSON, DAVID · 2014 to 2018
$14.8M
Multiplex RNA imaging in single cells by superresolution microscopy& barcode FISHR01HD075605 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAI, LONG, SOMLO, GEORGE NONE · 2012 to 2016
$4.1M
Howard Hughes Medical InstituteNHGRI NIH HHS U54 HG006998NHGRI NIH HHS U54 HG007990NICHD NIH HHS R01 HD075605NICHD NIH HHS R01HD075605A
6 · The paper itself

Abstract

Cellular reprogramming highlights the epigenetic plasticity of the somatic cell state. Long noncoding RNAs (lncRNAs) have emerging roles in epigenetic regulation, but their potential functions in reprogramming cell fate have been largely unexplored. We used single-cell RNA sequencing to characterize the expression patterns of over 16,000 genes, including 437 lncRNAs, during defined stages of reprogramming to pluripotency. Self-organizing maps (SOMs) were used as an intuitive way to structure and interrogate transcriptome data at the single-cell level. Early molecular events during reprogramming involved the activation of Ras signaling pathways, along with hundreds of lncRNAs. Loss-of-function studies showed that activated lncRNAs can repress lineage-specific genes, while lncRNAs activated in multiple reprogramming cell types can regulate metabolic gene expression. Our findings demonstrate that reprogramming cells activate defined sets of functionally relevant lncRNAs and provide a resource to further investigate how dynamic changes in the transcriptome reprogram cell state.

Indexed as

AnimalsCell LineageCellular ReprogrammingGene Expression Regulation, DevelopmentalGenes, DevelopmentalHematopoiesisInduced Pluripotent Stem CellsMicePluripotent Stem Cellsras ProteinsRNA, Long NoncodingSignal TransductionSingle-Cell AnalysisTranscriptomeras ProteinsRNA, Long Noncoding

Identifiers

PMID25575081
PMCPMC4291542
OpenAlexW1987754123

What OpenQuestion holds

Textmetadata
LicenceTDM
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.