Evidence map›Paper›PMID 38717553›Full record

ArticleCellular and molecular life sciences : CMLS2024

The IMPDH cytoophidium couples metabolism and fetal development in mice.

Min Peng, Gerson D Keppeke, Li-Kuang Tsai, Chia-Chun Chang, Ji-Long Liu, Li-Ying Sung

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. An IMPDH2 variant associated with neurodevelopmental disorder disrupts purine biosynthesis and somite organization.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Review
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

6 authors.

Min PengInstitute of Biotechnology, National Taiwan University, Taipei, 106, Taiwan.ORCID http://orcid.org/0000-0002-5675-0607
Gerson D KeppekeSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.ORCID http://orcid.org/0000-0003-0660-2857
Li-Kuang TsaiInstitute of Biotechnology, National Taiwan University, Taipei, 106, Taiwan.ORCID http://orcid.org/0000-0002-5714-4879
Chia-Chun ChangInstitute of Biotechnology, National Taiwan University, Taipei, 106, Taiwan. d01642003@ntu.edu.tw.ORCID http://orcid.org/0000-0001-7942-6300
Ji-Long LiuSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China. liujl3@shanghaitech.edu.cn.ORCID http://orcid.org/0000-0002-4834-8554
Li-Ying SungInstitute of Biotechnology, National Taiwan University, Taipei, 106, Taiwan. liyingsung@ntu.edu.tw.ORCID http://orcid.org/0000-0003-1221-2476

Funding

Medical Research Council MC_UU_12021/3; MC_U137788471
6 · The paper itself

Abstract

The cytoophidium is an evolutionarily conserved subcellular structure formed by filamentous polymers of metabolic enzymes. In vertebrates, inosine monophosphate dehydrogenase (IMPDH), which catalyses the rate-limiting step in guanosine triphosphate (GTP) biosynthesis, is one of the best-known cytoophidium-forming enzymes. Formation of the cytoophidium has been proposed to alleviate the inhibition of IMPDH, thereby facilitating GTP production to support the rapid proliferation of certain cell types such as lymphocytes, cancer cells and pluripotent stem cells (PSCs). However, past studies lacked appropriate models to elucidate the significance of IMPDH cytoophidium under normal physiological conditions. In this study, we demonstrate that the presence of IMPDH cytoophidium in mouse PSCs correlates with their metabolic status rather than pluripotency. By introducing IMPDH2 Y12C point mutation through genome editing, we established mouse embryonic stem cell (ESC) lines incapable of forming IMPDH polymers and the cytoophidium. Our data indicate an important role of IMPDH cytoophidium in sustaining a positive feedback loop that couples nucleotide biosynthesis with upstream metabolic pathways. Additionally, we find that IMPDH2 Y12C mutation leads to decreased cell proliferation and increased DNA damage in teratomas, as well as impaired embryo development following blastocoel injection. Further analysis shows that IMPDH cytoophidium assembly in mouse embryonic development begins after implantation and gradually increases throughout fetal development. These findings provide insights into the regulation of IMPDH polymerisation in embryogenesis and its significance in coordinating cell metabolism and development.

Indexed as

Cell ProliferationIMP DehydrogenaseAnimalsCellular StructuresDNA DamageFemaleFetal DevelopmentGuanosine TriphosphateMiceMice, Inbred C57BLPluripotent Stem CellsGuanosine TriphosphateIMP DehydrogenaseCytoophidiumEmbryonic developmentEnzyme polymerisationGTP biosynthesisIMPDHPluripotent stem cells

Identifiers

PMID38717553
PMCPMC11078715

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Registered trials

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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.