{"title":"Sequence characteristics, evolutionary history and expression pattern of BCO2 in Chinese mitten crab Eriocheir sinensis","authors":"Yanan Gao , Maolei Wei , Jingyi Xiong , Min Zhang , Xugan Wu","doi":"10.1016/j.cbd.2025.101524","DOIUrl":null,"url":null,"abstract":"<div><div>β-carotene 9’, 10’-oxygenase (BCO2) is a pivotal enzyme in the carotenoid cleavage. To fill the research gap of BCO2 in Chinese mitten crab <em>Eriocheir sinensis</em>, we first investigated <em>ESIN_BCO2</em> gene from its genome, revealing its evolutionary history, gene structure, and expression patterns. The results showed that E<em>SIN_BCO2</em> gene has a full-length open reading frame (ORF) of 1572 bp, encoding a protein of 523 amino acids. BCO2 was characterized by ten conserved motifs and an RPE65 domain, belonging to carotenoid cleavage oxygenase (CCO) family. Phylogenetic analysis revealed that <em>BCO1</em> was the ancestral gene, from which <em>BCO2</em> and <em>NinaB</em> diverged during evolution. Notably, the Ka/Ks ratios for BCO2 in Decapoda were approximately lower than BCO2 from other crustaceans (0.014 to 0.045 vs 0.112 to 0.185). <em>ESIN_BCO2</em> was predominantly expressed in the hindgut, with significantly higher expression levels in females than in males. It was predominantly localized near the nuclei (N) of <em>epi</em>thelial cells (epi) and basal cells (bc) in the hindgut. Moreover, dietary β-carotene supplementation significantly upregulated <em>BCO2</em> expression in the female hindgut. These findings provide valuable insights into the evolution and function of <em>BCO2</em> in <em>E. sinensis</em> as well as the other crustaceans, potentially shedding light on the conservation and divergence of carotenoid metabolism mechanisms across diverse crustaceans.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"56 ","pages":"Article 101524"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X25001133","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
β-carotene 9’, 10’-oxygenase (BCO2) is a pivotal enzyme in the carotenoid cleavage. To fill the research gap of BCO2 in Chinese mitten crab Eriocheir sinensis, we first investigated ESIN_BCO2 gene from its genome, revealing its evolutionary history, gene structure, and expression patterns. The results showed that ESIN_BCO2 gene has a full-length open reading frame (ORF) of 1572 bp, encoding a protein of 523 amino acids. BCO2 was characterized by ten conserved motifs and an RPE65 domain, belonging to carotenoid cleavage oxygenase (CCO) family. Phylogenetic analysis revealed that BCO1 was the ancestral gene, from which BCO2 and NinaB diverged during evolution. Notably, the Ka/Ks ratios for BCO2 in Decapoda were approximately lower than BCO2 from other crustaceans (0.014 to 0.045 vs 0.112 to 0.185). ESIN_BCO2 was predominantly expressed in the hindgut, with significantly higher expression levels in females than in males. It was predominantly localized near the nuclei (N) of epithelial cells (epi) and basal cells (bc) in the hindgut. Moreover, dietary β-carotene supplementation significantly upregulated BCO2 expression in the female hindgut. These findings provide valuable insights into the evolution and function of BCO2 in E. sinensis as well as the other crustaceans, potentially shedding light on the conservation and divergence of carotenoid metabolism mechanisms across diverse crustaceans.
期刊介绍:
Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology.
Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.