Biology subjects

Gibert, Y.

Publications and source records attributed to Gibert, Y..

4 recordsLinked to original sources

bioRxiv2026

An evolvable and functionally partitioned network underlies developmental remodelling in teleosts

Comparative embryology has revealed that early animal development is based on highly conserved genetic programs. Beyond embryogenesis however, animals undergo remarkably diverse post-embryonic developmental transitions such as metamorphosis. Whether these transitions are also organised into conserved genetic programs remains largely unexplored. To identify conserved genetic programs underlying post-embryonic development, we examine metamorphic remodelling in five teleost fishes, spanning 200 million years of evolution. By integrating comparative co-expression networks, evolutionary genomics, phylogenetic modelling, and functional data in zebrafish, we uncovered a conserved post-embryonic developmental network. This conserved network comprises components involved in core cellular processes, and involved in development and physiology, both of which are under the control of thyroid hormone during metamorphosis. Despite evolutionary conservation at the coding sequence level, this network exhibits significant turnover in gene family copy number following the teleost-specific whole-genome duplication as well as lineage-specific expansions and contractions. The variation in gene copy numbers is associated with macroevolutionary variation in a number of ecological and morphological traits, including swimming performance, and trophic level. Cross-species tissue expression, zebrafish single-cell transcriptomics, and zebrafish perturbation phenotypes placed the implicated genes in biological contexts relevant to these traits. Together, our results provide evidence of an ancient, functionally partitioned post-embryonic developmental network that has diversified throughout teleost evolution. The heterochronic variation in network function, changes in endocrine activity, and gene-family turnover provide potential routes through which a shared developmental architecture contributed to the evolution of phenotypic diversity in teleosts.

evolutionary biology↗

bioRxiv2025

Decoding the constraints acting on a coastal fish using landscape transcriptomics

Understanding how wild organisms respond to complex mixtures of environmental stressors remains a major challenge in ecology1,2. To move beyond laboratory-based studies of the effect of individual stressors on model species, landscape transcriptomics - the study of how genome-wide expression patterns reveal environmental conditions - has been suggested3. Here, we apply landscape transcriptomics to the damselfish Chrysiptera cyanea, a sentinel species from Okinawas coastal ecosystems, by sampling juveniles and adults across 18 sites from natural to urbanized habitats. We uncover a striking molecular signature of urbanization: fish from human-impacted sites exhibit elevated expression of genes involved in inflammation and immune responses. Remarkably, their transcriptomes resemble those of overfed individuals from laboratory feeding experiments - suggesting that urban reefs act as "fast food" environments, offering energy-rich diets while imposing chronic stress. This pattern is illustrated by the altered expression of key genes in metabolic and stress pathways (e.g., downregulation of ppargc1a and insrb, indicative of dietary intake surplus and insulin resistance; upregulation of interleukins, chemokines, toll-like receptors and caspase linked to the immune response and inflammation). Our results demonstrate that wild transcriptomes capture the invisible biological costs of environmental degradation, positioning fish as living biosensors for coastal ecosystem health.

bioinformatics↗

bioRxiv2024

From Genes to Pathways: A Curated Gene Approach to Accurate Pathway Reconstruction in Teleost Fish Transcriptomics

Interpreting the vast amounts of data generated by high-throughput sequencing technologies can often present a significant challenge, particularly for non-model organism. While automated approaches like GO (Gene Ontology) and KEGG (Kyoto Encyclopedia of Genes and Genomes) enrichment analyses are widely used, they often lack specificity for non-model organisms. To bridge this gap, we present a manually curated gene list tailored for teleost fish transcriptomics. This resource focuses on key biological processes crucial for understanding teleost fish physiology, development, and adaptation, including hormone signaling, various metabolic pathways, appetite regulation, digestion, gastrointestinal function, vision, ossification, osmoregulation, and pigmentation. Developed through collaborative efforts of specialists in diverse fields, the list prioritizes genes with established roles in teleost physiology, experimental evidence, and conservation across species. This curated list aims to provide researchers with a reliable starting point for transcriptomic analyses, offering a carefully evaluated set of genes relevant to current research priorities. By streamlining the process of gene selection and interpretation, this resource supports the broader teleost fish research community in designing and analyzing studies that investigate molecular responses to developmental and environmental changes. We encourage the scientific community to collaboratively expand and refine this list, ensuring its continued relevance and utility for teleost fish research.

systems biology↗

bioRxiv2022

The multi-level regulation of clownfish metamorphosis by thyroid hormones

Most marine organisms have a biphasic life cycle during which a pelagic larva is transformed into a radically different juvenile. In vertebrates the role of thyroid hormones (TH) in triggering this transition is well known, but how the morphological and physiological changes are integrated in a coherent way with the ecological transition remains poorly explored. To gain insight into this question, we performed an integrative analysis of metamorphosis of a marine teleost, the clownfish Amphiprion ocellaris. We reveal how TH coordinate a change in color vision as well as a major metabolic shift in energy production, hence highlighting its central integrative role in regulating this transformation. By manipulating the activity of LXR, a major regulator of metabolism, we also reveal a tight link between metabolic changes and metamorphosis progression. Strikingly, we observed that these regulations are at play in the wild revealing how hormones coordinate energy needs with available resources during life cycle.

developmental biology↗