Evidence map›Paper›PMID 36896912›Full record

ArticleThe EMBO journal2023

A mitochondrial SCF-FBXL4 ubiquitin E3 ligase complex degrades BNIP3 and NIX to restrain mitophagy and prevent mitochondrial disease.

Yu Cao, Jing Zheng, Huayun Wan, Yuqiu Sun, Song Fu, Shanshan Liu, Baiyu He, Gaihong Cai, Yang Cao, Huanwei Huang and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
21.7field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 101 citations in OpenAlex.

  1. Review
  2. Regulation and roles of mammalian mitophagy.Nature reviews. Molecular cell biology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Sustained loss ofbioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Function and regulation of the mitochondrial stress response.Nature structural & molecular biology · 2026
    Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Yu CaoCollege of Life Sciences, Beijing Normal University, Beijing, China.
Jing ZhengNational Institute of Biological Sciences, Beijing, China.
Huayun WanNational Institute of Biological Sciences, Beijing, China.
Yuqiu SunNational Institute of Biological Sciences, Beijing, China.ORCID 0000-0002-0047-2089
Song FuNational Institute of Biological Sciences, Beijing, China.
Shanshan LiuNational Institute of Biological Sciences, Beijing, China.ORCID 0000-0001-8293-1025
Baiyu HeNational Institute of Biological Sciences, Beijing, China.
Gaihong CaiNational Institute of Biological Sciences, Beijing, China.
Yang CaoNational Institute of Biological Sciences, Beijing, China.
Huanwei HuangNational Institute of Biological Sciences, Beijing, China.
Qi LiNational Institute of Biological Sciences, Beijing, China.
Yan MaNational Institute of Biological Sciences, Beijing, China.
She ChenNational Institute of Biological Sciences, Beijing, China.
Fengchao WangNational Institute of Biological Sciences, Beijing, China.
Hui JiangCollege of Life Sciences, Beijing Normal University, Beijing, China.ORCID 0000-0002-0277-9711
National Institute of Biological Sciences, Beijing · CNBeijing Normal University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitophagy is a fundamental quality control mechanism of mitochondria. Its regulatory mechanisms and pathological implications remain poorly understood. Here, via a mitochondria-targeted genetic screen, we found that knockout (KO) of FBXL4, a mitochondrial disease gene, hyperactivates mitophagy at basal conditions. Subsequent counter screen revealed that FBXL4-KO hyperactivates mitophagy via two mitophagy receptors BNIP3 and NIX. We determined that FBXL4 functions as an integral outer-membrane protein that forms an SCF-FBXL4 ubiquitin E3 ligase complex. SCF-FBXL4 ubiquitinates BNIP3 and NIX to target them for degradation. Pathogenic FBXL4 mutations disrupt SCF-FBXL4 assembly and impair substrate degradation. Fbxl4

Indexed as

Mitochondrial DiseasesMitophagyAnimalsMiceMitochondriaMitochondrial ProteinsUbiquitin-Protein LigasesUbiquitinsMitochondrial ProteinsUbiquitin-Protein LigasesUbiquitinsBNIP3/NIXFBXL4mitochondrial diseasemitophagyubiquitin-proteasome pathway

Identifiers

PMID36896912
PMCPMC10308365
OpenAlexW4323812485

What OpenQuestion 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 OpenQuestion graph.