Evidence map›Paper›PMID 35344438›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Genome-wide CRISPR screen reveals CLPTM1L as a lipid scramblase required for efficient glycosylphosphatidylinositol biosynthesis.

Yicheng Wang, Anant K Menon, Yuta Maki, Yi-Shi Liu, Yugo Iwasaki, Morihisa Fujita, Paula A Guerrero, Daniel Varó'n Silva, Peter H Seeberger, Yoshiko Murakami and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  6. Erk5-mediated microglial ferroptosis drives ischemic white matter damage via the Nfatc4-Clptm1l axis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Free GPIs and Comparison of GPI Structures Among Species.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
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  13. Article
  14. Insertases scramble lipids: Molecular simulations of MTCH2.Structure (London, England : 1993) · 2024
    Article
  15. Review
  16. Review
  17. Review
  18. Insertases Scramble Lipids: Molecular Simulations of MTCH2.bioRxiv : the preprint server for biology · 2023
    Article
  19. Article
  20. 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

11 authors at 6 institutions in 4 countries.

Yicheng WangResearch Institute for Microbial Diseases, Osaka University, 565-0871 Osaka, Japan.ORCID 0000-0001-7789-1938
Anant K MenonDepartment of Biochemistry, Weill Cornell Medical College, New York, NY 10065.ORCID 0000-0001-6924-2698
Yuta MakiDepartment of Chemistry, Graduate School of Science, Osaka University, 560-0043 Osaka, Japan.ORCID 0000-0002-5838-302X
Yi-Shi LiuKey Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 214122 Wuxi, China.ORCID 0000-0001-5640-1899
Yugo IwasakiGraduate School of Bioagricultural Science, Nagoya University, 464-8601 Aichi, Japan.ORCID 0000-0003-2784-9269
Morihisa FujitaKey Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, 214122 Wuxi, China.
Paula A GuerreroDepartment of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany.ORCID 0000-0002-4546-6010
Daniel Varó'n SilvaDepartment of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany.
Peter H SeebergerDepartment of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany.ORCID 0000-0003-3394-8466
Yoshiko MurakamiResearch Institute for Microbial Diseases, Osaka University, 565-0871 Osaka, Japan.ORCID 0000-0002-4870-5734
Taroh KinoshitaResearch Institute for Microbial Diseases, Osaka University, 565-0871 Osaka, Japan.ORCID 0000-0001-7166-7257
Max Planck Institute of Colloids and Interfaces · DEThe University of Osaka · JPJiangnan University · CNCornell University · USNagoya University · JPOsaka International Cancer Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SignificanceScramblases translocate lipids across the lipid bilayer without consumption of ATP, thereby regulating lipid distributions in cellular membranes. Cytosol-to-lumen translocation across the endoplasmic reticulum (ER) membrane is a common process among lipid glycoconjugates involved in posttranslational protein modifications in eukaryotes. These translocations are thought to be mediated by specific ER-resident scramblases, but the identity of these proteins and the underlying molecular mechanisms have been elusive. Here, we show that CLPTM1L, an integral membrane protein with eight putative transmembrane domains, is the major lipid scramblase involved in efficient glycosylphosphatidylinositol biosynthesis in the ER membrane. Our results validate the long-standing hypothesis that lipid scramblases ensure the efficient translocations of lipid glycoconjugates across the ER membrane for protein glycosylation pathways.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsGlycosylphosphatidylinositolsEndoplasmic ReticulumLipogenesisMembrane ProteinsGlycosylphosphatidylinositolsMembrane ProteinsCLPTM1Lendoplasmic reticulumglycobiologyglycosylphosphatidylinositolscramblase

Identifiers

PMID35344438
PMCPMC9169118
OpenAlexW4220799574

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.