Evidence map›Paper›PMID 39982420›Full record

ArticleBiology of reproduction2025

Disruption of oocyte SUMOylation impacts critical regulatory processes during folliculogenesis in mice†.

Zian Liao, Tessa E Steenwinkel, Bruno Moscoso, Ernesto Salas, Bethany K Patton, Amanda Rodriguez, Anna Malovannaya, Stephanie A Pangas

Abstract read
In one paragraph

Article in Biology of reproduction, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Zian LiaoDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.
Tessa E SteenwinkelDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.
Bruno MoscosoDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.
Ernesto SalasDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.
Bethany K PattonDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.
Amanda RodriguezDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.
Anna MalovannayaDepartment of Biochemistry and Molecular Pharmacology, Houston, TX, United States.
Stephanie A PangasDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States.

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Comprehensive Mechanisms in Reproductive SciencesT32HD098068 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI STEPHANIE A. PANGAS · 2020 to 2026
$2.4M
Protein Sumoylation in OOCYTE DevelopmentR01HD085994 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI PANGAS, STEPHANIE A. · 2017 to 2021
$1.6M
Cardiovascular Research and Drug Development (CRDD) training programT32HL170967 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Xander H.T. Wehrens, Damian Winston Young · 2024 to 2026
$830k
THERMO SCIENTIFIC Q EXACTIVE HF-X HYBRID QUADRUPOLE-ORBITRAP MASS SPECTROMETERS10OD026804 · OD · BAYLOR COLLEGE OF MEDICINE · PI MALOVANNAYA, ANNA · 2019 to 2019
$717k
A functional neddylation pathway underlies oocyte quality and agingR21HD109807 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI PANGAS, STEPHANIE A. · 2022 to 2023
$440k
NCI NIH HHS P30 CA125123NHLBI NIH HHS T32 HL170967NICHD NIH HHS R01 HD085994NICHD NIH HHS R21 HD109807NICHD NIH HHS T32 HD098068NICHD NIH HHS T32 HD098968NIH HHS S10 OD026804
6 · The paper itself

Abstract

The conjugation of small ubiquitin-like modifiers (SUMO) to target proteins, known as SUMOylation, plays a crucial role in regulating protein homeostasis, activity, interaction with other proteins, and subcellular localization. Loss of SUMOylation in nongrowing oocytes by conditional deletion of the E2 SUMO conjugating enzyme, Ube2i, at the primordial follicle stage leads to female sterility due to complex changes in oocyte development, including altered folliculogenesis, defective meiotic progression, and premature loss of the ovarian reserve. In this study, proteomics was used to compare control and Ube2i conditional knockout ovaries during the first wave of folliculogenesis to identify key differences that may drive the premature follicle loss phenotype. Label-free mass spectrometry results showed that 238 proteins were significantly altered more than 2-fold (p < 0.05). Proteins upregulated in the Ube2i conditional knockout ovaries included those involved in mRNA splicing and WNT signaling, while those downregulated were related to metabolism, mitochondria, and the maternal effect proteins NLRP2 and NLRP9B. The majority of differentially expressed proteins showed no change by transcriptome analysis, indicating protein level regulation and revealing potential SUMOylation targets with necessary roles in oocyte and follicle development.

Indexed as

OocytesOogenesisOvarian FollicleSumoylationAnimalsFemaleMiceMice, KnockoutUbiquitin-Conjugating EnzymesUbiquitin-Conjugating Enzymesfolliculogenesisinfertilityovaryposttranslational protein modificationproteomicsSUMOylation

Identifiers

PMID39982420
PMCPMC13017552

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.