Evidence map›Paper›PMID 40762086›Full record

ArticleMolecular ecology2025

Time-Series RNA-Seq of Acropora tenuis Reveals Molecular Waves Leading to Synchronous Mass Spawning of Scleractinian Corals.

Yuki Yoshioka, Go Suzuki, Yuji Fujikura, Satokuni Tashiro, Taiga Uchida, Eiichi Shoguchi, Noriyuki Satoh, Chuya Shinzato

Abstract read
In one paragraph

Article in Molecular ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Yuki YoshiokaMarine Genomics Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Okinawa, Japan.ORCID https://orcid.org/0000-0001-6348-4629
Go SuzukiFisheries Technology Institute, Japan Fisheries Research and Education Agency, Okinawa, Japan.
Yuji FujikuraFisheries Technology Institute, Japan Fisheries Research and Education Agency, Okinawa, Japan.
Satokuni TashiroFisheries Technology Institute, Japan Fisheries Research and Education Agency, Okinawa, Japan.
Taiga UchidaAtmosphere and Ocean Research Institute (AORI), The University of Tokyo, Chiba, Japan.ORCID https://orcid.org/0000-0002-3776-7032
Eiichi ShoguchiMarine Genomics Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Okinawa, Japan.
Noriyuki SatohMarine Genomics Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Okinawa, Japan.
Chuya ShinzatoAtmosphere and Ocean Research Institute (AORI), The University of Tokyo, Chiba, Japan.ORCID https://orcid.org/0000-0001-7843-3381

Funding

Japan Society for the Promotion of Science JP20H03066Japan Society for the Promotion of Science JP20H03235Japan Society for the Promotion of Science JP20J21301Japan Society for the Promotion of Science JP20K21860Japan Society for the Promotion of Science JP23KJ2129Japan Society for the Promotion of Science JP24K01847
6 · The paper itself

Abstract

Although mass, synchronised spawning of scleractinian corals is a well-known phenomenon, its underlying molecular mechanisms, especially those that achieve synchronous release of gametes, are still unknown. In the genus Acropora, the dominant scleractinian coral in shallow reefs, spawning timing is synchronised in any given location, but often varies among locations. Here, we report gene expression cascades potentially driving synchronous mass spawning, revealed through transcriptome monitoring of Acropora tenuis, tracking both daily and monthly dynamics during a year-long experiment that included two spawning events. We identified 236 genes in four waves of molecular events that culminated in spawning. First, receptor function and prostaglandin secretion became active 2 weeks before spawning and gradually decreased, but remained elevated until spawning, suggesting communication of maturation among colonies. Second, 1-2 weeks before spawning, TGF-β signalling and spermiogenesis involving kinases were activated. Third, sperm capacitation and preparation of egg-sperm bundle material commenced a week before spawning. Finally, activation of transcription factor ELF1 triggered a signal cascade that induced spawning. This moonlight-independent system may serve to fine-tune the timing of spawning and may explain the broad geographic distribution and ecological success of Acropora, making it the most diverse and abundant genus of scleractinian corals in reef ecosystems.

Indexed as

AnthozoaAnimalsCoral ReefsMaleReproductionRNA-SeqTranscriptomeAcropora tenuislong‐term monitoringreef‐building coralssimultaneous mass spawningtime‐series RNA‐seq

Identifiers

PMID40762086
PMCPMC12573721

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.