Evidence map›Paper›PMID 27466324›Full record

ArticleEMBO reports2016

Ubiquitously expressed genes participate in cell-specific functions via alternative promoter usage.

Guihai Feng, Man Tong, Baolong Xia, Guan-Zheng Luo, Meng Wang, Dongfang Xie, Haifeng Wan, Ying Zhang, Qi Zhou, Xiu-Jie Wang

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Guihai FengState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology Chinese Academy of Sciences, Beijing, China Key Laboratory of Genetic Network Biology, Collaborative Innovation Center of Genetics and Development Institute of Genetics and Developmental Biology Chinese Academy of Sciences, Beijing, China.
Man TongKey Laboratory of Genetic Network Biology, Collaborative Innovation Center of Genetics and Development Institute of Genetics and Developmental Biology Chinese Academy of Sciences, Beijing, China.
Baolong XiaState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology Chinese Academy of Sciences, Beijing, China University of Chinese Academy of Sciences, Beijing, China.
Guan-Zheng LuoKey Laboratory of Genetic Network Biology, Collaborative Innovation Center of Genetics and Development Institute of Genetics and Developmental Biology Chinese Academy of Sciences, Beijing, China.
Meng WangKey Laboratory of Genetic Network Biology, Collaborative Innovation Center of Genetics and Development Institute of Genetics and Developmental Biology Chinese Academy of Sciences, Beijing, China.
Dongfang XieKey Laboratory of Genetic Network Biology, Collaborative Innovation Center of Genetics and Development Institute of Genetics and Developmental Biology Chinese Academy of Sciences, Beijing, China.
Haifeng WanState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology Chinese Academy of Sciences, Beijing, China.
Ying ZhangState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology Chinese Academy of Sciences, Beijing, China.
Qi ZhouState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology Chinese Academy of Sciences, Beijing, China qzhou@ioz.ac.cn xjwang@genetics.ac.cn.
Xiu-Jie WangKey Laboratory of Genetic Network Biology, Collaborative Innovation Center of Genetics and Development Institute of Genetics and Developmental Biology Chinese Academy of Sciences, Beijing, China qzhou@ioz.ac.cn xjwang@genetics.ac.cn.ORCID 0000-0001-7865-0204
Chinese Academy of Sciences · CNInstitute of Genetics and Developmental Biology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How do different cell types acquire their specific identities and functions is a fundamental question of biology. Previously significant efforts have been devoted to search for cell-type-specifically expressed genes, especially transcription factors, yet how do ubiquitously expressed genes participate in the formation or maintenance of cell-type-specific features remains largely unknown. Here, we have identified 110 mouse embryonic stem cell (mESC) specifically expressed transcripts with cell-stage-specific alternative transcription start sites (SATS isoforms) from 104 ubiquitously expressed genes, majority of which have active epigenetic modification- or stem cell-related functions. These SATS isoforms are specifically expressed in mESCs, and tend to be transcriptionally regulated by key pluripotency factors through direct promoter binding. Knocking down the SATS isoforms of Nmnat2 or Usp7 leads to differentiation-related phenotype in mESCs. These results demonstrate that cell-type-specific transcription factors are capable to produce cell-type-specific transcripts with alternative transcription start sites from ubiquitously expressed genes, which confer ubiquitously expressed genes novel functions involved in the establishment or maintenance of cell-type-specific features.

Indexed as

Gene Expression RegulationPromoter Regions, GeneticAnimalsDNA Transposable ElementsEmbryonic Stem CellsFibroblastsMiceNicotinamide-Nucleotide AdenylyltransferaseOrgan SpecificityProtein BindingTranscription FactorsTranscription Initiation SiteUbiquitin-Specific Peptidase 7Ubiquitin-Specific ProteasesDNA Transposable ElementsNicotinamide-Nucleotide AdenylyltransferaseNmnat2 protein, mouseTranscription FactorsUbiquitin-Specific Peptidase 7Ubiquitin-Specific ProteasesUsp7 protein, mouseembryonic stem cellpluripotency factorsstage‐specific alternative transcription start sitesubiquitously expressed genes

Identifiers

PMID27466324
PMCPMC5007564
OpenAlexW2500341763

What OpenQuestion holds

Textmetadata
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.