Sully Mak
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Sully Mak has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
Aurélien Brionne
Institut National de Recherche pour l'Agriculture l'Alimentation et l'Environnement
1 shared publication- Benoît Delahaye
Nantes Université, Centrale Nantes, CNRS, LS2N UMR CNRS 6004
1 shared publication Fabrice Mahé
Université de Rennes
1 shared publication- Guillaume Cantin
Nantes Université, Centrale Nantes, CNRS, LS2N UMR CNRS 6004
1 shared publication - Julien Bobe
INRAE
1 shared publication Jérôme Montfort
Institut National de Recherche pour l'Agriculture l'Alimentation et l'Environnement
1 shared publication
Latest Publications
- 11 October 2026
- Published by Springer Nature
- p. 140-154
Formal Analysis of Hybrid Systems Using Parametric Statistical Model Checking
- 11 October 2026
- Published by Springer Nature
- p. 140-154
Formal Analysis of Hybrid Systems Using Parametric Statistical Model Checking
- Open Access
Identification of miR-187 as a modulator of early oogenesis and female fecundity in medaka
MicroRNAs (miRNAs) are known regulators of ovarian function in vertebrates, yet their physiological roles in fish reproduction remain poorly understood. Here, we identified miR-187 as one of the most ovarian-enriched miRNAs in medaka (Oryzias latipes) and we uncovered its function in vivo using CRISPR/Cas9-mediated gene inactivation. miR-187-3p is expressed in oocytes and granulosa cells in the ovary, and in discrete brain areas. Its loss-of-function leads to a significant reduction in female fecundity. High-resolution 3D imaging of whole ovaries revealed that mir-187 mutants accumulate early stage I follicles and show reduced progression to later stages, indicating a defect in early follicle recruitment and growth. Transcriptomic profiling of mutant ovaries revealed extensive gene-expression remodeling, including downregulation of key regulators of steroidogenesis, Wnt/β-catenin signaling, and TGF-β pathways, and upregulation of genes associated with early follicle activation and immature somatic cell states. Using an expression-based target-prediction pipeline, we identified several putative miR-187-3p targets, including nr6a1a (gcnf) and dpagt1, two genes previously implicated in oocyte differentiation and female fertility in mammals. Together, our results demonstrate that miR-187 acts as a previously unrecognized regulator of early folliculogenesis and female reproductive capacity in medaka, expanding the repertoire of miRNAs with essential in vivo roles in teleost oogenesis and female fecundity.
Open AccessIdentification of miR-187 as a modulator of early oogenesis and female fecundity in medaka
MicroRNAs (miRNAs) are known regulators of ovarian function in vertebrates, yet their physiological roles in fish reproduction remain poorly understood. Here, we identified miR-187 as one of the most ovarian-enriched miRNAs in medaka (Oryzias latipes) and we uncovered its function in vivo using CRISPR/Cas9-mediated gene inactivation. miR-187-3p is expressed in oocytes and granulosa cells in the ovary, and in discrete brain areas. Its loss-of-function leads to a significant reduction in female fecundity. High-resolution 3D imaging of whole ovaries revealed that mir-187 mutants accumulate early stage I follicles and show reduced progression to later stages, indicating a defect in early follicle recruitment and growth. Transcriptomic profiling of mutant ovaries revealed extensive gene-expression remodeling, including downregulation of key regulators of steroidogenesis, Wnt/β-catenin signaling, and TGF-β pathways, and upregulation of genes associated with early follicle activation and immature somatic cell states. Using an expression-based target-prediction pipeline, we identified several putative miR-187-3p targets, including nr6a1a (gcnf) and dpagt1, two genes previously implicated in oocyte differentiation and female fertility in mammals. Together, our results demonstrate that miR-187 acts as a previously unrecognized regulator of early folliculogenesis and female reproductive capacity in medaka, expanding the repertoire of miRNAs with essential in vivo roles in teleost oogenesis and female fecundity.