Evidence map›Paper›PMID 36062884›Full record

ArticlePhysiological genomics2022

Global phosphoproteomic profiling of skeletal muscle in ovarian hormone-deficient mice.

Mina P Peyton, Tzu-Yi Yang, LeeAnn Higgins, Todd W Markowski, Cha Vue, Laurie L Parker, Dawn A Lowe

Open access · greenAbstract read
In one paragraph

Article in Physiological genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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  7. Ablation of skeletal muscle estrogen receptor alpha impairs contractility in male mice.Journal of applied physiology (Bethesda, Md. : 1985) · 2024
    Article
  8. Article
  9. Article
  10. Highlighting recent impactful publications inPhysiological genomics · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Mina P PeytonDivision of Rehabilitation Science, Department of Rehabilitation Medicine, University of Minnesota, Twin Cities, Minneapolis, Minnesota.ORCID 0000-0002-0250-1429
Tzu-Yi YangDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Twin Cities, Minneapolis, Minnesota.
LeeAnn HigginsDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Twin Cities, Minneapolis, Minnesota.
Todd W MarkowskiDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Twin Cities, Minneapolis, Minnesota.
Cha VueDivision of Rehabilitation Science, Department of Rehabilitation Medicine, University of Minnesota, Twin Cities, Minneapolis, Minnesota.
Laurie L ParkerDepartment of Computer Science, Bioinformatics and Computational Biology Program, University of Minnesota, Minneapolis, Minnesota.
Dawn A LoweDivision of Rehabilitation Science, Department of Rehabilitation Medicine, University of Minnesota, Twin Cities, Minneapolis, Minnesota.ORCID 0000-0002-5784-9289
University of Minnesota · US

Funding

TRAINING PROGRAM IN MUSCLE RESEARCHT32AR007612 · NIAMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JAMES M ERVASTI, DAWN A LOWE · 2001 to 2026
$11.3M
Interatction of Estrogen, Age and Activity on Musculoskeletal Strength in FemalesR01AG031743 · NIA · UNIVERSITY OF MINNESOTA · PI DAWN A LOWE · 2009 to 2026
$7.4M
NIAMS NIH HHS T32 AR007612NIA NIH HHS R01 AG031743
6 · The paper itself

Abstract

Protein phosphorylation is important in skeletal muscle development, growth, regeneration, and contractile function. Alterations in the skeletal muscle phosphoproteome due to aging have been reported in males; however, studies in females are lacking. We have demonstrated that estrogen deficiency decreases muscle force, which correlates with decreased myosin regulatory light chain phosphorylation. Thus, we questioned whether the decline of estrogen in females that occurs with aging might alter the skeletal muscle phosphoproteome. C57BL/6J female mice (6 mo) were randomly assigned to a sham-operated (Sham) or ovariectomy (Ovx) group to investigate the effects of estrogen deficiency on skeletal muscle protein phosphorylation in a resting, noncontracting condition. After 16 wk of estrogen deficiency, the tibialis anterior muscle was dissected and prepped for label-free nano-liquid chromatography-tandem mass spectrometry phosphoproteomic analysis. We identified 4,780 phosphopeptides in tibialis anterior muscles of ovariectomized (Ovx) and Sham-operated (Sham) control mice. Further analysis revealed 647 differentially regulated phosphopeptides (Benjamini-Hochberg adjusted

Indexed as

Myosin Light ChainsPhosphopeptidesAnimalsEstrogensFemaleMiceMice, Inbred C57BLMuscle, SkeletalEstrogensMyosin Light ChainsPhosphopeptidesAMPKestrogenfemalesovariectomyYAP

Identifiers

PMID36062884
PMCPMC9639773
OpenAlexW4294667244

What Socratic 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 Socratic graph.