Evidence map›Paper›PMID 42098280›Full record

ArticleCommunications biology2026

Germ granule components regulate endosomal switching during the oocyte-to-embryo transition in Caenorhabditis elegans.

Shun-Ichi Suto, Koh-Ichi Teraoka, Ichiro Kawasaki, Kenta Sugiura, Taeko Sasaki, Ikuko Maejima, Hidetaka Kosako, Miyuki Sato, Ken Sato

Abstract read
In one paragraph

Article in Communications biology, 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

9 authors.

Shun-Ichi Suto *Laboratory of Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.ORCID http://orcid.org/0009-0008-8140-7481
Koh-Ichi Teraoka *Laboratory of Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.
Ichiro Kawasaki *Laboratory of Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.ORCID http://orcid.org/0000-0003-1722-0993
Kenta SugiuraLaboratory of Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.ORCID http://orcid.org/0000-0002-4264-6737
Taeko SasakiLaboratory of Molecular Membrane Biology, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.ORCID http://orcid.org/0000-0003-1521-2076
Ikuko MaejimaLaboratory of Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.ORCID http://orcid.org/0000-0002-0396-5890
Hidetaka KosakoDivision of Cell Signaling, Institute of Advanced Medical Sciences, Tokushima University, Tokushima, Japan.ORCID http://orcid.org/0000-0003-3228-6368
Miyuki SatoLaboratory of Molecular Membrane Biology, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan. m-sato@gunma-u.ac.jp.ORCID http://orcid.org/0000-0002-1944-4918
Ken SatoLaboratory of Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, Japan. sato-ken@gunma-u.ac.jp.ORCID http://orcid.org/0000-0002-1034-5091

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
MEXT | Japan Society for the Promotion of Science (JSPS) 20H00466MEXT | Japan Society for the Promotion of Science (JSPS) 23KJ0291MEXT | Japan Society for the Promotion of Science (JSPS) 25H00987MEXT | Japan Society for the Promotion of Science (JSPS) 25K02268MEXT | Japan Society for the Promotion of Science (JSPS) 26H00910MEXT | Japan Society for the Promotion of Science (JSPS) 26H01038NIH HHS P40 OD010440Takeda Science Foundation 2024095741
6 · The paper itself

Abstract

The egg cytoplasm undergoes large-scale remodeling after fertilization. Here, we reveal that the germ granule component, HERD-1, is involved in selective degradation of maternal plasma membrane proteins after fertilization in Caenorhabditis elegans. HERD-1 is specifically expressed in the germline and mainly localized in a subtype of germ granules, Z granules. HERD-1 loss caused maternal plasma membrane protein accumulation in ubiquitin-positive early and late endosomal assemblies in the early embryos. The proteomic analysis showed that HERD-1 loss substantially reduced the protein levels of a subset of endolysosomal regulators such as ESCRT-0 components regulating the multivesicular body pathway. Defects in maternal membrane protein degradation in herd-1-deficient embryos were suppressed with the loss of DEPS-1 or PRG-1, which are required for germ granule organization and small-RNA biogenesis. These results suggest that several germ granule components maintain appropriate endolysosomal component levels via small RNA-mediated regulation during the oocyte-to-embryo transition, promoting endosomal switching toward embryogenesis.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsEndosomesOocytesAnimalsCytoplasmic GranulesEmbryonic DevelopmentEmbryo, NonmammalianFemaleCaenorhabditis elegans Proteins

Identifiers

PMID42098280
PMCPMC13365812

What Socratic 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 Socratic graph.