Evidence mapPaperPMID 42329921Full record

ArticlePLoS genetics2026

Lysosome-related organelles employ divergent mechanisms to modulate cytosolic zinc homeostasis.

Chaoyi Xie, Yi Luo, Yawen Zheng, Bowen Liu, Shibo Song, Jie Wei, Anbing Shi, Yanling Yan

Abstract read
In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Chaoyi XieDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0009-0005-8419-3528
Yi LuoDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Yawen ZhengDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Bowen LiuDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0009-0002-7417-7186
Shibo SongDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0009-0007-6388-3321
Jie WeiDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Anbing ShiDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0000-0003-1128-2026
Yanling YanDepartment of Biochemistry and Molecular Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Disease, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID https://orcid.org/0000-0002-9145-1872

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated environmental zinc levels pose significant toxicity to biological systems, necessitating adaptive responses to mitigate excessive zinc exposure. In C. elegans, a specific lysosome-related organelle, the gut granule, may increase in number and volume with high dietary zinc, thereby lowering cytosolic zinc concentration, though the mechanisms remain unclear. Our results suggest that GLO-1 predominantly controls granule biogenesis, whereas zinc-induced granule expansion involves distinct mechanisms. Further study revealed that high zinc upregulated GLO-1 activity through its GEF complex GLO-3-CCZ-1, by enhancing transcription of GLO-3 and post-translational modification of CCZ-1. Zinc transporter CDF-2 has been identified to mediate zinc influx into gut granules. In this study, analysis of 14 C. elegans CDFs reveals that ZK185.5 (CDF-3) and F19C6.5 (CDF-4) also localize in gut granules. Functional studies suggest that CDF-3, not CDF-4, complements CDF-2 in facilitating zinc influx into gut granules. Unlike CDF-2, the expression of CDF-3 is downregulated in a high zinc diet. These results suggest a modulation in the composition of CDFs within gut granules in response to environmental zinc. Together, our study reveals a sophisticated zinc detoxification mechanism of C. elegans gut granule to uphold cytosolic zinc homeostasis amidst fluctuating environments.

Indexed as

Caenorhabditis elegans ProteinsLysosomesZincAnimalsCaenorhabditis elegansCarrier ProteinsCytoplasmic GranulesCytosolHomeostasisCaenorhabditis elegans ProteinsCarrier ProteinsZinc

Identifiers

PMID42329921
PMCPMC13286216

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.