Evidence map›Paper›PMID 38470362›Full record

ArticleThe Journal of cell biology2024

p24-Tango1 interactions ensure ER-Golgi interface stability and efficient transport.

Ke Yang, Zhi Feng, José Carlos Pastor-Pareja

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Role ofInternational journal of molecular sciences · 2025
    Article
  6. Review
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Ke YangSchool of Life Sciences, Tsinghua University , Beijing, China.ORCID 0000-0002-5545-497X
Zhi FengSchool of Life Sciences, Tsinghua University , Beijing, China.ORCID 0000-0002-9740-0435
José Carlos Pastor-ParejaSchool of Life Sciences, Tsinghua University , Beijing, China.ORCID 0000-0002-3823-4473
Tsinghua University · CNUniversitat de Miguel Hernández d'Elx · ES

Funding

CSICMinisterio de Ciencia e Innovación PID2021-122119NB-I00National Natural Science Foundation of China 32150710524Severo Ochoa CEX2021-001165-S
6 · The paper itself

Abstract

The eukaryotic p24 family, consisting of α-, β-, γ- and δ-p24 subfamilies, has long been known to be involved in regulating secretion. Despite increasing interest in these proteins, fundamental questions remain about their role. Here, we systematically investigated Drosophila p24 proteins. We discovered that members of all four p24 subfamilies are required for general secretion and that their localizations between ER exit site (ERES) and Golgi are interdependent in an α→βδ→γ sequence. We also found that localization of p24 proteins and ERES determinant Tango1 requires interaction through their respective GOLD and SH3 lumenal domains, with Tango1 loss sending p24 proteins to the plasma membrane and vice versa. Finally, we show that p24 loss expands the COPII zone at ERES and increases the number of ER-Golgi vesicles, supporting a restrictive role of p24 proteins on vesicle budding for efficient transport. Our results reveal Tango1-p24 interplay as central to the generation of a stable ER-Golgi interface.

Indexed as

Aryl Hydrocarbon Receptor Nuclear TranslocatorDrosophila ProteinsEndoplasmic ReticulumGolgi ApparatusMembrane Transport ProteinsCell MembraneDrosophila melanogastersrc Homology DomainsAryl Hydrocarbon Receptor Nuclear TranslocatorDrosophila ProteinsMembrane Transport Proteinstgo protein, Drosophila

Identifiers

PMID38470362
PMCPMC10932740
OpenAlexW4392703421

What Socratic holds

Textmetadata
LicenceCC BY
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.