Evidence map›Paper›PMID 34473253›Full record

ArticleDevelopment (Cambridge, England)2021

Y705 and S727 are required for the mitochondrial import and transcriptional activities of STAT3, and for regulation of stem cell proliferation.

Margherita Peron, Alberto Dinarello, Giacomo Meneghetti, Laura Martorano, Riccardo M Betto, Nicola Facchinello, Annachiara Tesoriere, Natascia Tiso, Graziano Martello, Francesco Argenton

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.0field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Role of the STAT3 Signaling Pathway in Cell Proliferation and Inflammation in Psoriasis and Approaches for Targeted Therapies: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
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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 1 institution in 1 country.

Margherita PeronDepartment of Biology, University of Padova, 35121, Padova, Italy.
Alberto DinarelloDepartment of Biology, University of Padova, 35121, Padova, Italy.
Giacomo MeneghettiDepartment of Biology, University of Padova, 35121, Padova, Italy.
Laura MartoranoDepartment of Biology, University of Padova, 35121, Padova, Italy.
Riccardo M BettoDepartment of Molecular Medicine, University of Padova, 35121, Padova, Italy.ORCID 0000-0001-5083-0668
Nicola FacchinelloDepartment of Biology, University of Padova, 35121, Padova, Italy.ORCID 0000-0003-4898-4064
Annachiara TesoriereDepartment of Biology, University of Padova, 35121, Padova, Italy.
Natascia TisoDepartment of Biology, University of Padova, 35121, Padova, Italy.ORCID 0000-0002-5444-9853
Graziano MartelloDepartment of Biology, University of Padova, 35121, Padova, Italy.ORCID 0000-0001-5520-085X
Francesco ArgentonDepartment of Biology, University of Padova, 35121, Padova, Italy.ORCID 0000-0002-0803-8236
University of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The STAT3 transcription factor, acting both in the nucleus and mitochondria, maintains embryonic stem cell pluripotency and promotes their proliferation. In this work, using zebrafish, we determined in vivo that mitochondrial STAT3 regulates mtDNA transcription in embryonic and larval stem cell niches and that this activity affects their proliferation rates. As a result, we demonstrated that import of STAT3 inside mitochondria requires Y705 phosphorylation by Jak, whereas its mitochondrial transcriptional activity, as well as its effect on proliferation, depends on the MAPK target S727. These data were confirmed using mouse embryonic stem cells: although the Y705-mutated STAT3 cannot enter mitochondria, the S727 mutation does not affect import into the organelle and is responsible for STAT3-dependent mitochondrial transcription. Surprisingly, STAT3-dependent increase of mitochondrial transcription appears to be independent from STAT3 binding to STAT3-responsive elements. Finally, loss-of-function experiments, with chemical inhibition of the JAK/STAT3 pathway or genetic ablation of stat3 gene, demonstrated that STAT3 is also required for cell proliferation in the intestine of zebrafish.

Indexed as

Cell ProliferationAnimalsCentral Nervous SystemDNA, MitochondrialEmbryonic Stem CellsEmbryo, NonmammalianExtracellular Signal-Regulated MAP KinasesIntestinesJanus KinasesMitochondriaMutationPhosphorylationSignal TransductionSTAT3 Transcription FactorTranscriptional ActivationTranscription, GeneticDNA, MitochondrialExtracellular Signal-Regulated MAP KinasesJanus Kinasesstat3 protein, zebrafishSTAT3 Transcription FactorZebrafish ProteinsEmbryonic stem cellsMitochondriaSTAT3TranscriptionZebrafish

Identifiers

PMID34473253
PMCPMC8451946
OpenAlexW3197958221

What OpenQuestion holds

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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.