Evidence map›Paper›PMID 14673173›Full record

ArticleMolecular and cellular biology2004

Essential role of STAT3 in postnatal survival and growth revealed by mice lacking STAT3 serine 727 phosphorylation.

Yuhong Shen, Karni Schlessinger, Xuejun Zhu, Eric Meffre, Fred Quimby, David E Levy, J E Darnell

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing 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

106 citing papers in PubMed.

  1. Article
  2. Review
  3. The βCirculation research · 2025
    Article
  4. Article
  5. Article
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  7. Article
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  9. Article
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  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Epilepsy in Pregnancy-Management Principles and Focus on Valproate.International journal of molecular sciences · 2022
    Review
  20. Article

46 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

7 authors.

Yuhong ShenLaboratory of Molecular Cell Biology, The Rockefeller University, New York, New York 10021, USA.
Karni Schlessinger
Xuejun Zhu
Eric Meffre
Fred Quimby
David E Levy
J E Darnell

Funding

STAT Activation: Inactivation Cycle and Activated STAT3 in Cancer CellsR01AI032489 · NIAID · ROCKEFELLER UNIVERSITY · PI DARNELL, JAMES E · 1991 to 2010
$5.1M
GENE ACTIVATION BY POLYPEPTIDES--CELL SURFACE TO NUCLEUSR37AI034420 · NIAID · ROCKEFELLER UNIVERSITY · PI DARNELL, JAMES E · 1999 to 2008
$3.1M
GENE ACTIVATION BY POLYPEPTIDES--CELL SURFACE TO NUCLEUSR01AI034420 · NIAID · ROCKEFELLER UNIVERSITY · PI DARNELL, JAMES E · 1994 to 1998
–
NIAID NIH HHS AI32489NIAID NIH HHS AI34420NIAID NIH HHS R01 AI032489NIAID NIH HHS R37 AI034420
6 · The paper itself

Abstract

A large number of extracellular polypeptides bound to their cognate receptors activate the transcription factor STAT3 by phosphorylation of tyrosine 705. Supplemental activation occurs when serine 727 is also phosphorylated. STAT3 deletion in mice leads to embryonic lethality. We have produced mice with alanine substituted for serine 727 in STAT3 (the SA allele) to examine the function of serine 727 phosphorylation in vivo. Embryonic fibroblasts from SA/SA mice had approximately 50% of the transcriptional response of wild-type cells. However, SA/SA mice were viable and grossly normal. STAT3 wild-type/null (+/-) animals were also normal and were interbred with SA/SA mice to study SA/- mice. The SA/- mice progressed through gestation, showing 10 to 15% reduced birth weight, three-fourths died soon after birth, and the SA/- survivors reached only 50 to 60% of normal size at 1 week of age. The lethality and decreased growth were accompanied by altered insulin-like growth factor 1 (IGF-1) levels in serum, establishing a role for the STAT3 serine phosphorylation acting through IGF-1 in embryonic and perinatal growth. The SA/- survivors have decreased thymocyte number associated with increased apoptosis, but unexpectedly normal STAT3-dependent liver acute phase response. These animals offer the opportunity to study defined reductions in the transcriptional capacity of a widely used signaling pathway.

Indexed as

AnimalsDNA-Binding ProteinsFibroblastsGenes, LethalGenes, RecessiveInsulin-Like Growth Factor IMiceMutationPhosphorylationSerineSTAT3 Transcription FactorThymus GlandTrans-ActivatorsTranscription, GeneticDNA-Binding ProteinsInsulin-Like Growth Factor ISerineStat3 protein, mouseSTAT3 Transcription FactorTrans-Activators

Identifiers

PMID14673173
PMCPMC303338

What OpenQuestion holds

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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.