<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gomez-Campo K</submitter><funding>Pennsylvania State University</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>e17246</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10922902</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(4)</volume><pubmed_abstract>Acclimatization through phenotypic plasticity represents a more rapid response to environmental change than adaptation and is vital to optimize organisms' performance in different conditions. Generally, animals are less phenotypically plastic than plants, but reef-building corals exhibit plant-like properties. They are light dependent with a sessile and modular construction that facilitates rapid morphological changes within their lifetime. We induced phenotypic changes by altering light exposure in a reciprocal transplant experiment and found that coral plasticity is a colony trait emerging from comprehensive morphological and physiological changes within the colony. Plasticity in skeletal features optimized coral light harvesting and utilization and paralleled significant methylome and transcriptome modifications. Network-associated responses resulted in the identification of hub genes and clusters associated to the change in phenotype: inter-partner recognition and phagocytosis, soft tissue growth and biomineralization. Furthermore, we identified hub genes putatively involved in animal photoreception-phototransduction. These findings fundamentally advance our understanding of how reef-building corals repattern the methylome and adjust a phenotype, revealing an important role of light sensing by the coral animal to optimize photosynthetic performance of the symbionts.</pubmed_abstract><journal>Molecular ecology</journal><pubmed_title>Phenotypic plasticity for improved light harvesting, in tandem with methylome repatterning in reef-building corals.</pubmed_title><pmcid>PMC10922902</pmcid><funding_grant_id>NIH R01 GM134056‐01</funding_grant_id><funding_grant_id>NSF OCE‐1537959</funding_grant_id><funding_grant_id>R01 GM134056</funding_grant_id><funding_grant_id>NIH R01 GM134056-01</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Gomez-Campo K</pubmed_authors><pubmed_authors>Sanchez R</pubmed_authors><pubmed_authors>Enriquez S</pubmed_authors><pubmed_authors>Iglesias-Prieto R</pubmed_authors><pubmed_authors>Baums IB</pubmed_authors><pubmed_authors>Maher T</pubmed_authors><pubmed_authors>Martinez-Rugerio I</pubmed_authors><pubmed_authors>Osborne CC</pubmed_authors><pubmed_authors>Mackenzie SA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phenotypic plasticity for improved light harvesting, in tandem with methylome repatterning in reef-building corals.</name><description>Acclimatization through phenotypic plasticity represents a more rapid response to environmental change than adaptation and is vital to optimize organisms' performance in different conditions. Generally, animals are less phenotypically plastic than plants, but reef-building corals exhibit plant-like properties. They are light dependent with a sessile and modular construction that facilitates rapid morphological changes within their lifetime. We induced phenotypic changes by altering light exposure in a reciprocal transplant experiment and found that coral plasticity is a colony trait emerging from comprehensive morphological and physiological changes within the colony. Plasticity in skeletal features optimized coral light harvesting and utilization and paralleled significant methylome and transcriptome modifications. Network-associated responses resulted in the identification of hub genes and clusters associated to the change in phenotype: inter-partner recognition and phagocytosis, soft tissue growth and biomineralization. Furthermore, we identified hub genes putatively involved in animal photoreception-phototransduction. These findings fundamentally advance our understanding of how reef-building corals repattern the methylome and adjust a phenotype, revealing an important role of light sensing by the coral animal to optimize photosynthetic performance of the symbionts.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-06-01T18:11:49.316Z</modification><creation>2025-04-05T19:20:06.47Z</creation></dates><accession>S-EPMC10922902</accession><cross_references><pubmed>38153177</pubmed><doi>10.1111/mec.17246</doi></cross_references></HashMap>