ArticleMarine biotechnology (New York, N.Y.)2026
Deciphering Gamete Differentiation in Ostrea edulis using Laser Capture Microdissection and RNA-seq.
Article in Marine biotechnology (New York, N.Y.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Molluscs exhibit high sexual plasticity, with sequential hermaphroditism being particularly widespread among oysters. Although some key gene pathways are conserved, the transcriptional regulatory networks controlling the gamete development in oysters remain limited. The European flat oyster, Ostrea edulis, serves as an ideal model for deciphering this alternating protandrous hermaphroditism. This study used a laser capture microdissection (LCM) coupled with bulk RNA sequencing approach to investigate the transcriptomic dynamics during gamete development. This study showed that gonia cells represent an immature, proliferative, and highly plastic germ-cell population, with a transcriptomic program largely shared between the male and female developmental pathways. We evidence the importance of transcriptional reprogramming during the transition from gonia cells to primary spermatocytes, the extensive remodeling of the gonadal microenvironment at the secondary spermatocyte stage and the role of lipid metabolism and membrane remodeling in the spermatid maturation. We also characterized that early oocyte development is associated with activation of meiotic, cell-cycle, proteostasis, and metabolic pathways and that oocyte maturation involves coordinated genome maintenance, ovarian differentiation, nutrient accumulation, and epigenetic regulation. This study is the first conducted in O edulis describing in details both spermatogenesis and oogenesis, evidencing new molecular pathways that are still poorly studied in oysters.
Indexed as
Identifiers
42776277What Socratic holds
Registered trials
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.