Fanhua Sun , Sihua Kou , Huan Liao , Zhengrui Zhang , Jingjing Kong , Xindong Cui , Zujing Yang , Zhenmin Bao , Xiaoting Huang
{"title":"MCM基因的鉴定、表征和表达分析揭示了MCM基因在低ph胁迫下的调控作用。","authors":"Fanhua Sun , Sihua Kou , Huan Liao , Zhengrui Zhang , Jingjing Kong , Xindong Cui , Zujing Yang , Zhenmin Bao , Xiaoting Huang","doi":"10.1016/j.cbd.2025.101591","DOIUrl":null,"url":null,"abstract":"<div><div>The Yesso scallop (<em>Patinopecten yessoensis</em>), an ecomically important bivalve species, exhibits high susceptibility to ocean acidification. The growth retardation induced by low-pH stress poses a significant challenge for Yesso scallop aquaculture. However, the molecular mechanisms underlying this phenomenon are not well understood. Considering the pivotal role of cell proliferation in organism growth, we investigated the minichromosome maintenance (MCM) family in <em>P. yessoensis</em>, which are key regulators of DNA replication initiation and cell cycle regulation. In this study, we identified nine MCM genes (<em>PyMCM2–10</em>) in the <em>P. yessoensis</em> genome. These <em>PyMCMs</em> exhibit highly conserved sequence characteristics and typical MCM domains. Phylogenetic analysis showed that <em>PyMCMs</em> cluster into nine distinct clades, underscoring their strong evolutionary conservation across species homologs. Spatiotemporal expression profiling demonstrated widespread expressions of <em>PyMCMs</em> throughout all developmental stages and adult tissues, with particularly high levels in vigorous cell proliferation (<em>e.g.</em>, up to 318 TPM in multicell stage and up to 202 TPM in gonad tissue). Notably, <em>PyMCM6</em> exhibited consistently high expression across development and across tissues (> 44 TPM), suggesting a key regulatory role in both development and tissue maintenance. Under low-pH stress, the expressions of <em>PyMCMs</em> were downregulated to varying degrees, with <em>PyMCM5</em> showing the most significant reduction (|log<sub>2</sub>FC| up to 3.5), while <em>PyMCM8</em> and <em>PyMCM9</em> remained relatively stable. This pattern suggests a strategic response that scallops reduce DNA replication capacity (mediated by <em>PyMCM2–7</em>) but potentially maintain DNA repair functions (associated with <em>PyMCM8/9</em> stability) to mitigate damage induced by low-pH, potentially explaining the intrinsic inhibition of cell proliferation. Quantitative real-time PCR and <em>in situ</em> hybridization further confirmed that low-pH stress inhibits <em>PyMCMs</em> expressions (<em>p</em> < 0.05), with the effect amplified as pH decreases. Collectively, these findings enhance our understanding of <em>PyMCMs</em> in regulating bivalve growth retardation under low-pH stress and provide valuable insights into the mechanisms of environmental adaptation in bivalves.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"56 ","pages":"Article 101591"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification, characterization, and expression analysis reveal regulatory roles of MCM genes in Patinopecten yessoensis under low-pH stress\",\"authors\":\"Fanhua Sun , Sihua Kou , Huan Liao , Zhengrui Zhang , Jingjing Kong , Xindong Cui , Zujing Yang , Zhenmin Bao , Xiaoting Huang\",\"doi\":\"10.1016/j.cbd.2025.101591\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The Yesso scallop (<em>Patinopecten yessoensis</em>), an ecomically important bivalve species, exhibits high susceptibility to ocean acidification. The growth retardation induced by low-pH stress poses a significant challenge for Yesso scallop aquaculture. However, the molecular mechanisms underlying this phenomenon are not well understood. Considering the pivotal role of cell proliferation in organism growth, we investigated the minichromosome maintenance (MCM) family in <em>P. yessoensis</em>, which are key regulators of DNA replication initiation and cell cycle regulation. In this study, we identified nine MCM genes (<em>PyMCM2–10</em>) in the <em>P. yessoensis</em> genome. These <em>PyMCMs</em> exhibit highly conserved sequence characteristics and typical MCM domains. Phylogenetic analysis showed that <em>PyMCMs</em> cluster into nine distinct clades, underscoring their strong evolutionary conservation across species homologs. Spatiotemporal expression profiling demonstrated widespread expressions of <em>PyMCMs</em> throughout all developmental stages and adult tissues, with particularly high levels in vigorous cell proliferation (<em>e.g.</em>, up to 318 TPM in multicell stage and up to 202 TPM in gonad tissue). Notably, <em>PyMCM6</em> exhibited consistently high expression across development and across tissues (> 44 TPM), suggesting a key regulatory role in both development and tissue maintenance. Under low-pH stress, the expressions of <em>PyMCMs</em> were downregulated to varying degrees, with <em>PyMCM5</em> showing the most significant reduction (|log<sub>2</sub>FC| up to 3.5), while <em>PyMCM8</em> and <em>PyMCM9</em> remained relatively stable. This pattern suggests a strategic response that scallops reduce DNA replication capacity (mediated by <em>PyMCM2–7</em>) but potentially maintain DNA repair functions (associated with <em>PyMCM8/9</em> stability) to mitigate damage induced by low-pH, potentially explaining the intrinsic inhibition of cell proliferation. Quantitative real-time PCR and <em>in situ</em> hybridization further confirmed that low-pH stress inhibits <em>PyMCMs</em> expressions (<em>p</em> < 0.05), with the effect amplified as pH decreases. Collectively, these findings enhance our understanding of <em>PyMCMs</em> in regulating bivalve growth retardation under low-pH stress and provide valuable insights into the mechanisms of environmental adaptation in bivalves.</div></div>\",\"PeriodicalId\":55235,\"journal\":{\"name\":\"Comparative Biochemistry and Physiology D-Genomics & Proteomics\",\"volume\":\"56 \",\"pages\":\"Article 101591\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-07-29\",\"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/S1744117X25001807\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X25001807","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}
Identification, characterization, and expression analysis reveal regulatory roles of MCM genes in Patinopecten yessoensis under low-pH stress
The Yesso scallop (Patinopecten yessoensis), an ecomically important bivalve species, exhibits high susceptibility to ocean acidification. The growth retardation induced by low-pH stress poses a significant challenge for Yesso scallop aquaculture. However, the molecular mechanisms underlying this phenomenon are not well understood. Considering the pivotal role of cell proliferation in organism growth, we investigated the minichromosome maintenance (MCM) family in P. yessoensis, which are key regulators of DNA replication initiation and cell cycle regulation. In this study, we identified nine MCM genes (PyMCM2–10) in the P. yessoensis genome. These PyMCMs exhibit highly conserved sequence characteristics and typical MCM domains. Phylogenetic analysis showed that PyMCMs cluster into nine distinct clades, underscoring their strong evolutionary conservation across species homologs. Spatiotemporal expression profiling demonstrated widespread expressions of PyMCMs throughout all developmental stages and adult tissues, with particularly high levels in vigorous cell proliferation (e.g., up to 318 TPM in multicell stage and up to 202 TPM in gonad tissue). Notably, PyMCM6 exhibited consistently high expression across development and across tissues (> 44 TPM), suggesting a key regulatory role in both development and tissue maintenance. Under low-pH stress, the expressions of PyMCMs were downregulated to varying degrees, with PyMCM5 showing the most significant reduction (|log2FC| up to 3.5), while PyMCM8 and PyMCM9 remained relatively stable. This pattern suggests a strategic response that scallops reduce DNA replication capacity (mediated by PyMCM2–7) but potentially maintain DNA repair functions (associated with PyMCM8/9 stability) to mitigate damage induced by low-pH, potentially explaining the intrinsic inhibition of cell proliferation. Quantitative real-time PCR and in situ hybridization further confirmed that low-pH stress inhibits PyMCMs expressions (p < 0.05), with the effect amplified as pH decreases. Collectively, these findings enhance our understanding of PyMCMs in regulating bivalve growth retardation under low-pH stress and provide valuable insights into the mechanisms of environmental adaptation in bivalves.
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.