Pub Date : 2025-05-12eCollection Date: 2025-05-01DOI: 10.1007/s42995-025-00299-5
Yajun Wang, Gaoqian Xu, Haoyi Li, Jing Gao, Xueqing Du, Wanyue Jiang, Guangdong Ji, Zhenhui Liu
Sex determination and differentiation play crucial biological roles in sexual reproduction in vertebrates, including zebrafish. Nevertheless, the intricate molecular mechanisms governing these processes have remained enigmatic. In this study, we showed a pivotal role played by zinc finger GATA-like protein-1 (Zglp-1) in sex differentiation in zebrafish. Our findings revealed that homozygous mutants having no Zglp-1 exhibited a female-to-male sex reversal, ultimately resulting in the development of fertile males. Within the pivotal phase of sexual differentiation, zglp-1-/- zebrafish demonstrated a gene expression pattern that was skewed toward a male phenotype. Notably, the expression of amh was upregulated, while the expression of cyp19a1a was not sustained. Furthermore, our data revealed a direct interaction between the zinc fingers of Zglp-1 and Sf-1, which inhibited the ability of Sf-1 to activate the amh promoter. This interaction was crucial for regulating sex differentiation. Moreover, we observed alterations in gonadal cell proliferation and apoptosis in zglp-1-/- zebrafish, which partially contributed to the sexual fate selection. Overall, our findings firmly established Zglp-1 as a crucial regulator of sex differentiation in zebrafish, offering deep insights into the intricate molecular mechanisms that govern sex determination and differentiation in vertebrates.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00299-5.
{"title":"Zglp-1 is a novel essential transcriptional regulator for sex reversal in zebrafish.","authors":"Yajun Wang, Gaoqian Xu, Haoyi Li, Jing Gao, Xueqing Du, Wanyue Jiang, Guangdong Ji, Zhenhui Liu","doi":"10.1007/s42995-025-00299-5","DOIUrl":"10.1007/s42995-025-00299-5","url":null,"abstract":"<p><p>Sex determination and differentiation play crucial biological roles in sexual reproduction in vertebrates, including zebrafish. Nevertheless, the intricate molecular mechanisms governing these processes have remained enigmatic. In this study, we showed a pivotal role played by zinc finger GATA-like protein-1 (Zglp-1) in sex differentiation in zebrafish. Our findings revealed that homozygous mutants having no Zglp-1 exhibited a female-to-male sex reversal, ultimately resulting in the development of fertile males. Within the pivotal phase of sexual differentiation, <i>zglp-1</i> <sup><i>-/-</i></sup> zebrafish demonstrated a gene expression pattern that was skewed toward a male phenotype. Notably, the expression of <i>amh</i> was upregulated, while the expression of <i>cyp19a1a</i> was not sustained. Furthermore, our data revealed a direct interaction between the zinc fingers of Zglp-1 and Sf-1, which inhibited the ability of Sf-1 to activate the <i>amh</i> promoter. This interaction was crucial for regulating sex differentiation. Moreover, we observed alterations in gonadal cell proliferation and apoptosis in <i>zglp-1</i> <sup><i>-/-</i></sup> zebrafish, which partially contributed to the sexual fate selection. Overall, our findings firmly established Zglp-1 as a crucial regulator of sex differentiation in zebrafish, offering deep insights into the intricate molecular mechanisms that govern sex determination and differentiation in vertebrates.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00299-5.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 2","pages":"256-270"},"PeriodicalIF":5.8,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102022/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144144335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Small cell lung cancer (SCLC) is a high-grade malignancy and prone to drug resistance, with limited progress in patient survival over the past 30 years. Therefore, there is an urgent need to explore new treatment strategies for SCLC patients. Autophagic cell death represents a novel therapeutic strategy for cancer cells with high apoptotic thresholds. Here, we demonstrate that nitrobenzoyl-insulicolide A (1), a new sesquiterpene, isolated from Antarctica sponge-derived fungus Aspergillus insulicola HDN151418, inhibits the proliferation of various SCLC cells including adriamycin- or cisplatin/etoposide-resistant cells, via autophagic death rather than apoptosis, necrosis and cell aging. Molecular mechanism analysis revealed that compound 1 induced autophagic cell death in the NCI-H446 and H69 AR cells dependent on activations of the AKT/mTOR/PARP and ERK1/2 signaling pathways. These findings provide an experimental basis for the further development of 1 as a lead compound against small cell lung cancer in future.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00292-y.
{"title":"Nitrobenzoyl-insulicolide A: a novel dinitrobenzoyl sesquiterpenoid, induces autophagic cell death in small cell lung cancer cells.","authors":"Yige Zhang, Xiaomin Zhang, Chunxiao Sun, Xin Qi, Dehai Li, Jing Li","doi":"10.1007/s42995-025-00292-y","DOIUrl":"https://doi.org/10.1007/s42995-025-00292-y","url":null,"abstract":"<p><p>Small cell lung cancer (SCLC) is a high-grade malignancy and prone to drug resistance, with limited progress in patient survival over the past 30 years. Therefore, there is an urgent need to explore new treatment strategies for SCLC patients. Autophagic cell death represents a novel therapeutic strategy for cancer cells with high apoptotic thresholds. Here, we demonstrate that nitrobenzoyl-insulicolide A (<b>1</b>), a new sesquiterpene, isolated from Antarctica sponge-derived fungus <i>Aspergillus insulicola</i> HDN151418, inhibits the proliferation of various SCLC cells including adriamycin- or cisplatin/etoposide-resistant cells, via autophagic death rather than apoptosis, necrosis and cell aging. Molecular mechanism analysis revealed that compound <b>1</b> induced autophagic cell death in the NCI-H446 and H69 AR cells dependent on activations of the AKT/mTOR/PARP and ERK1/2 signaling pathways. These findings provide an experimental basis for the further development of <b>1</b> as a lead compound against small cell lung cancer in future.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00292-y.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 4","pages":"949-961"},"PeriodicalIF":5.3,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662960/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145649726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-05-02eCollection Date: 2025-08-01DOI: 10.1007/s42995-025-00288-8
Yuhao Zhao, Chenxiao Wu, Chi Man Leong, Jiaxin Li, Wei Lu, Yijuan Xu, Xingfeng Si, Nathan J Sanders
Habitat fragmentation is a major cause of biodiversity loss. Fragmentation can alter thermal conditions on the remaining patches, especially at habitat edges, but few studies have examined variations in thermal tolerance of species in fragmented habitats. Ants are sensitive to both habitat fragmentation and temperature changes, and are an ideal taxon for studying these impacts. Here, we focused on the dimorphic ant species Pheidole nodus in a fragmented habitat island system (Thousand island lake) in China. We assessed critical thermal maximum (CTmax), minimum (CTmin), and range (CTrange) temperatures for both minor (workers) and major workers (soldiers) of 2307 individuals from 117 edge and interior colonies across 9 islands during relatively hot and cold seasons. Using mixed-effect linear models, we explored the effects of island area, habitat type (edge vs. interior), season, and caste (worker vs. soldier) on CTmax, CTmin, and CTrange. We found temperatures were 1-3 °C higher in edge than interior sites in relatively hot season. Yet, only CTmax and CTrange in edge populations were higher than those of interior sites on smaller islands. CTmax was higher in relatively hot season and CTmin was lower in relatively cold season, indicating seasonal plasticity in thermal tolerance. Workers consistently had higher CTmax and lower CTmin than soldiers. These findings underscore the importance of seasonality, worker caste, and interactive effect between island area and habitat type in shaping thermal tolerance of a dominant dimorphic ant species on fragmented habitat islands. Our study provides a roadmap for integrating thermal biology into studies of how fragmentation impacts biodiversity.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00288-8.
{"title":"Seasonality, worker caste, and the interaction between island area and habitat type influence the thermal tolerance of ants on fragmented habitat islands.","authors":"Yuhao Zhao, Chenxiao Wu, Chi Man Leong, Jiaxin Li, Wei Lu, Yijuan Xu, Xingfeng Si, Nathan J Sanders","doi":"10.1007/s42995-025-00288-8","DOIUrl":"10.1007/s42995-025-00288-8","url":null,"abstract":"<p><p>Habitat fragmentation is a major cause of biodiversity loss. Fragmentation can alter thermal conditions on the remaining patches, especially at habitat edges, but few studies have examined variations in thermal tolerance of species in fragmented habitats. Ants are sensitive to both habitat fragmentation and temperature changes, and are an ideal taxon for studying these impacts. Here, we focused on the dimorphic ant species <i>Pheidole nodus</i> in a fragmented habitat island system (Thousand island lake) in China. We assessed critical thermal maximum (CTmax), minimum (CTmin), and range (CTrange) temperatures for both minor (workers) and major workers (soldiers) of 2307 individuals from 117 edge and interior colonies across 9 islands during relatively hot and cold seasons. Using mixed-effect linear models, we explored the effects of island area, habitat type (edge vs. interior), season, and caste (worker vs. soldier) on CTmax, CTmin, and CTrange. We found temperatures were 1-3 °C higher in edge than interior sites in relatively hot season. Yet, only CTmax and CTrange in edge populations were higher than those of interior sites on smaller islands. CTmax was higher in relatively hot season and CTmin was lower in relatively cold season, indicating seasonal plasticity in thermal tolerance. Workers consistently had higher CTmax and lower CTmin than soldiers. These findings underscore the importance of seasonality, worker caste, and interactive effect between island area and habitat type in shaping thermal tolerance of a dominant dimorphic ant species on fragmented habitat islands. Our study provides a roadmap for integrating thermal biology into studies of how fragmentation impacts biodiversity.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00288-8.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 3","pages":"581-593"},"PeriodicalIF":5.3,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12413355/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145014432","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Phycobilisomes (PBS), the primary light-harvesting complexes in cyanobacteria, are degraded under nitrogen starvation to provide nitrogen for cell growth. This study reveals that carbon supply is a critical prerequisite for PBS degradation under nitrogen deficiency in Synechococcus sp. PCC 7002. Even under nitrogen-deficient conditions, PBS degradation is inhibited in the absence of sufficient carbon. We demonstrate that both the nblAB-mediated PBS-degradation pathway and the ccmLMNK operon-mediated CO2-concentrating mechanism are essential for PBS degradation. Furthermore, our findings highlight the critical role of PBS degradation in cyanobacterial adaptation to high C/N conditions. Mutant strains (Mut-nblA and Mut-nblB) deficient in PBS degradation exhibited impaired adaptation to high C/N conditions, as evidenced by their inability to thrive in high NaHCO3 (nitrogen-free) or CO2 (low-nitrogen) environments. While these mutants displayed a greener phenotype under high C/N conditions compared to the wild type, they exhibited extensive cellular damage, and significant downregulation of photosynthesis-related genes. These results provide novel insights into the carbon-dependent regulation of PBS degradation and its essential role in cyanobacterial C/N balance, highlighting its significance for their adaptation to fluctuating environmental conditions.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00290-0.
{"title":"Physiological and molecular evidence for phycobilisome degradation in maintaining carbon and nitrogen balance of cyanobacteria.","authors":"Zhen Luo, Shuangqing Li, Muhammad Zain Ul Arifeen, Fei-Xue Fu, Huayang Gao, Taoran Sun, Lingmei Liu, Xumei Sun, Xinwei Wang, Hai-Bo Jiang","doi":"10.1007/s42995-025-00290-0","DOIUrl":"10.1007/s42995-025-00290-0","url":null,"abstract":"<p><p>Phycobilisomes (PBS), the primary light-harvesting complexes in cyanobacteria, are degraded under nitrogen starvation to provide nitrogen for cell growth. This study reveals that carbon supply is a critical prerequisite for PBS degradation under nitrogen deficiency in <i>Synechococcus</i> sp. PCC 7002. Even under nitrogen-deficient conditions, PBS degradation is inhibited in the absence of sufficient carbon. We demonstrate that both the <i>nblAB</i>-mediated PBS-degradation pathway and the <i>ccmLMNK</i> operon-mediated CO<sub>2</sub>-concentrating mechanism are essential for PBS degradation. Furthermore, our findings highlight the critical role of PBS degradation in cyanobacterial adaptation to high C/N conditions. Mutant strains (Mut-<i>nblA</i> and Mut-<i>nblB)</i> deficient in PBS degradation exhibited impaired adaptation to high C/N conditions, as evidenced by their inability to thrive in high NaHCO<sub>3</sub> (nitrogen-free) or CO<sub>2</sub> (low-nitrogen) environments. While these mutants displayed a greener phenotype under high C/N conditions compared to the wild type, they exhibited extensive cellular damage, and significant downregulation of photosynthesis-related genes. These results provide novel insights into the carbon-dependent regulation of PBS degradation and its essential role in cyanobacterial C/N balance, highlighting its significance for their adaptation to fluctuating environmental conditions.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00290-0.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 2","pages":"218-230"},"PeriodicalIF":5.8,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102436/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144144213","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-25eCollection Date: 2025-08-01DOI: 10.1007/s42995-025-00291-z
Oleksandra Oskyrko, Chunrong Mi, Weiguo Du
Biological invasions represent one of the main anthropogenic drivers of global change with a substantial impact on biodiversity. Traditional studies predict invasion risk based on the correlation between species' distribution and environmental factors, with little attention to the potential contribution of physiological factors. In this study, we incorporated temperature-dependent sex determination (TSD) and sex-ratio data into species distribution models (SDMs) to assess the current and future suitable habitats for the world's worst invasive reptile species, the pond slider turtle (Trachemys scripta). First, occurrence records of T. scripta from online databases and published scientific literature were identified. Then, climatic variables representing current (1976-2013) and future (2060-2080) climate scenarios were extracted and combined with sex-ratio records to create hybrid-SDMs with which to assess the current and future suitable habitats for T. scripta. It was found that T. scripta has potential suitable habitat in 136 countries at present. Under the four climate change scenarios (ssp126, ssp245, ssp370 and ssp585) that were modeled, the distribution of T. scripta is predicted to decrease in 78-93 countries but increase in the northern hemisphere. This confirms that there is a greater likelihood that this species will increase in more developed countries. Incorporating the thermal dependence of sex ratio into hybrid-SDMs can be an important addition to detect the invasion risk of TSD species and to develop region-specific invasion management strategies to prevent and/or control invasive species such as T. scripta.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00291-z.
{"title":"Integrating the thermal dependence of sex ratio into distribution models to predict suitable habitats for the invasive freshwater pond slider turtle, <i>Trachemys scripta</i>.","authors":"Oleksandra Oskyrko, Chunrong Mi, Weiguo Du","doi":"10.1007/s42995-025-00291-z","DOIUrl":"10.1007/s42995-025-00291-z","url":null,"abstract":"<p><p>Biological invasions represent one of the main anthropogenic drivers of global change with a substantial impact on biodiversity. Traditional studies predict invasion risk based on the correlation between species' distribution and environmental factors, with little attention to the potential contribution of physiological factors. In this study, we incorporated temperature-dependent sex determination (TSD) and sex-ratio data into species distribution models (SDMs) to assess the current and future suitable habitats for the world's worst invasive reptile species, the pond slider turtle (<i>Trachemys scripta</i>). First, occurrence records of <i>T. scripta</i> from online databases and published scientific literature were identified. Then, climatic variables representing current (1976-2013) and future (2060-2080) climate scenarios were extracted and combined with sex-ratio records to create hybrid-SDMs with which to assess the current and future suitable habitats for <i>T. scripta</i>. It was found that <i>T. scripta</i> has potential suitable habitat in 136 countries at present. Under the four climate change scenarios (ssp126, ssp245, ssp370 and ssp585) that were modeled, the distribution of <i>T. scripta</i> is predicted to decrease in 78-93 countries but increase in the northern hemisphere. This confirms that there is a greater likelihood that this species will increase in more developed countries. Incorporating the thermal dependence of sex ratio into hybrid-SDMs can be an important addition to detect the invasion risk of TSD species and to develop region-specific invasion management strategies to prevent and/or control invasive species such as <i>T. scripta</i>.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00291-z.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 3","pages":"619-631"},"PeriodicalIF":5.3,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12413374/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145016695","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-24eCollection Date: 2025-05-01DOI: 10.1007/s42995-025-00282-0
Li-Ming He, Xuan Deng, Li-Hua Ni, Shi-Qi Cai, Jinhu Chen, Zejin Liao, Mengke Zhang, Hua Shui, Kong-Kai Zhu, Song Wu, Ping Gao, Ariel M Sarotti, Kui Hong, Xiao-Yan Wu, You-Sheng Cai
An investigation of the mangrove-derived fungus Penicillium sp. DM27 led to the isolation of 19 new compounds, including three pairs of piperidinone enantiomers ( ±)-1, ( ±)-2, and ( ±)-3, two pairs of pyrrolidinone enantiomers ( ±)-4 and ( ±)-5, and nine pyrrolidine derivatives 6-14. The structures of 1-14 were elucidated through NMR and HRESIMS analysis, coupled with experimental and calculated ECD spectroscopy and the modified Mosher method. Quantitative real time PCR and Western bolt analyses revealed that 11 blocked EMT in TGF-β1-treated HK-2 cells and suppressed fibroblast activation in TGF-β1-stimulated NIH-3T3 cells. Molecular simulations demonstrated that compound 11 could dock ADAM17, showing a high negative binding affinity. Additionally, the overexpression of ADAM17 by lentiviral infection triggered renal tubular EMT, while compound 11 suppressed this process. Overall, our research suggests that pyrrolidine derivatives may be potential therapeutic agents for the treatment of fibrotic kidney disease.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00282-0.
{"title":"Penicipyrrolidines A-N, pyrrolidine derivatives with inhibitory effects on EMT and fibroblast activation from the mangrove-derived fungus <i>Penicillium</i> sp. DM27.","authors":"Li-Ming He, Xuan Deng, Li-Hua Ni, Shi-Qi Cai, Jinhu Chen, Zejin Liao, Mengke Zhang, Hua Shui, Kong-Kai Zhu, Song Wu, Ping Gao, Ariel M Sarotti, Kui Hong, Xiao-Yan Wu, You-Sheng Cai","doi":"10.1007/s42995-025-00282-0","DOIUrl":"10.1007/s42995-025-00282-0","url":null,"abstract":"<p><p>An investigation of the mangrove-derived fungus <i>Penicillium</i> sp. DM27 led to the isolation of 19 new compounds, including three pairs of piperidinone enantiomers ( ±)-<b>1</b>, ( ±)-<b>2</b>, and ( ±)-<b>3</b>, two pairs of pyrrolidinone enantiomers ( ±)-<b>4</b> and ( ±)-<b>5</b>, and nine pyrrolidine derivatives <b>6</b>-<b>14</b>. The structures of <b>1</b>-<b>14</b> were elucidated through NMR and HRESIMS analysis, coupled with experimental and calculated ECD spectroscopy and the modified Mosher method. Quantitative real time PCR and Western bolt analyses revealed that <b>11</b> blocked EMT in TGF-β1-treated HK-2 cells and suppressed fibroblast activation in TGF-β1-stimulated NIH-3T3 cells. Molecular simulations demonstrated that compound <b>11</b> could dock ADAM17, showing a high negative binding affinity. Additionally, the overexpression of ADAM17 by lentiviral infection triggered renal tubular EMT, while compound <b>11</b> suppressed this process. Overall, our research suggests that pyrrolidine derivatives may be potential therapeutic agents for the treatment of fibrotic kidney disease.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00282-0.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 2","pages":"313-327"},"PeriodicalIF":5.8,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102406/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144144208","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-24eCollection Date: 2025-11-01DOI: 10.1007/s42995-025-00296-8
Jeong Sang Yi, Jin Won Choi, Ngoc Han Le Thi, Sung Jin Kim, Hyun-Ju Kim, Jung Min Kim, Jun Eui Park, Kyuho Moon, Dong Chan Oh, Sang Hee Shim, Ki Sung Kang, Yeo Joon Yoon
Analysis of the secondary metabolite biosynthesis gene cluster (BGC) from marine Streptomyces sp. SNJ102 revealed the presence of a noncanonical nonribosomal peptide synthetase (NRPS), predicted to produce a depsipeptide compound. The NRPS gene cluster was captured by transformation-associated recombination and heterologously expressed in Streptomyces albus. The production of the new compound was confirmed using high-resolution liquid chromatography-mass spectrometry, and its structure was elucidated using nuclear magnetic resonance spectroscopy. The structure of the new depsipeptide was more similar to the monomeric structure of cyclic depsipeptides derived from fungi than to other Streptomyces-derived depsipeptides. In addition, the bacterial depsipeptide, which we named jejumide, showed promising anti-inflammatory activity. These results demonstrate that genome mining and successful heterologous expression of cryptic nonlinear NRPS BGCs from marine bacteria will facilitate the discovery of novel nonribosomal peptides and understanding of the complicated biosynthetic mechanism of nonlinear NRPS.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00296-8.
{"title":"Transformation-associated recombination and heterologous expression of noncanonical depsipeptide nonribosomal peptide synthetase derived from marine <i>Streptomyces</i>.","authors":"Jeong Sang Yi, Jin Won Choi, Ngoc Han Le Thi, Sung Jin Kim, Hyun-Ju Kim, Jung Min Kim, Jun Eui Park, Kyuho Moon, Dong Chan Oh, Sang Hee Shim, Ki Sung Kang, Yeo Joon Yoon","doi":"10.1007/s42995-025-00296-8","DOIUrl":"10.1007/s42995-025-00296-8","url":null,"abstract":"<p><p>Analysis of the secondary metabolite biosynthesis gene cluster (BGC) from marine <i>Streptomyces</i> sp. SNJ102 revealed the presence of a noncanonical nonribosomal peptide synthetase (NRPS), predicted to produce a depsipeptide compound. The NRPS gene cluster was captured by transformation-associated recombination and heterologously expressed in <i>Streptomyces albus</i>. The production of the new compound was confirmed using high-resolution liquid chromatography-mass spectrometry, and its structure was elucidated using nuclear magnetic resonance spectroscopy. The structure of the new depsipeptide was more similar to the monomeric structure of cyclic depsipeptides derived from fungi than to other <i>Streptomyces</i>-derived depsipeptides. In addition, the bacterial depsipeptide, which we named jejumide, showed promising anti-inflammatory activity. These results demonstrate that genome mining and successful heterologous expression of cryptic nonlinear NRPS BGCs from marine bacteria will facilitate the discovery of novel nonribosomal peptides and understanding of the complicated biosynthetic mechanism of nonlinear NRPS.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00296-8.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 4","pages":"937-948"},"PeriodicalIF":5.3,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662965/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145650022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-21eCollection Date: 2025-11-01DOI: 10.1007/s42995-025-00287-9
Xiaoliang Wu, Xiaofang Liang, Min Li, Jiacheng Liu, Chunyu Ge, Xiaoze Xie, Jie Wang, Yinhua Zheng, Hao Wang, Xiufeng Wu, Xu Gu, Min Xue
Post-translational modifications (PTMs) regulate the activity and functionality of RELA, but their role in the pathogenesis of liver fibrosis is unclear. This study was performed to understand the regulation mechanism of acetylation of RELA on liver inflammation and fibrosis in a model animal of innate glucose intolerance, largemouth bass, and to provide a potential target and biomarker for liver fibrosis therapy. We found that the acetylation of total proteins and RELA was significantly reduced in fibrotic livers of largemouth bass induced by a high-carbohydrate and high-fat diet (HCHFD) and CCL4 challenge. Furthermore, quantitative acetylome data showed that the K119 site of RELA was deacetylated in fibrotic livers compared to healthy controls. Subsequently, we reveal a new mechanism that SIRT7 deacetylates RELA at the K119 site in largemouth bass. RELA K119 deacetylation enhances RELA transcriptional activity by increasing its DNA-binding activity, and facilitates nuclear translocation of RELA, resulting in the overwhelming release of proinflammatory factors, and subsequently enhancing liver inflammation and fibrosis. Pharmacological inhibition of SIRT7 using a specific inhibitor restores the decreased acetylation of RELA in vivo and in vitro, and reduces the transcriptional activity, nuclear localization of RELA and the expression of its target genes, which ultimately attenuates liver inflammation and fibrosis. These findings uncover a novel mechanism underlying liver fibrosis involving SIRT7-mediated deacetylation of RELA to activate the proinflammatory gene program, and thus provide important insights and biomarkers into the effective strategies for limiting liver inflammation and fibrosis.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00287-9.
{"title":"A novel RELA K119 deacetylation mediated by SIRT7 is a pivotal activator to exacerbate liver inflammation and fibrosis in teleosts.","authors":"Xiaoliang Wu, Xiaofang Liang, Min Li, Jiacheng Liu, Chunyu Ge, Xiaoze Xie, Jie Wang, Yinhua Zheng, Hao Wang, Xiufeng Wu, Xu Gu, Min Xue","doi":"10.1007/s42995-025-00287-9","DOIUrl":"10.1007/s42995-025-00287-9","url":null,"abstract":"<p><p>Post-translational modifications (PTMs) regulate the activity and functionality of RELA, but their role in the pathogenesis of liver fibrosis is unclear. This study was performed to understand the regulation mechanism of acetylation of RELA on liver inflammation and fibrosis in a model animal of innate glucose intolerance, largemouth bass, and to provide a potential target and biomarker for liver fibrosis therapy. We found that the acetylation of total proteins and RELA was significantly reduced in fibrotic livers of largemouth bass induced by a high-carbohydrate and high-fat diet (HCHFD) and CCL4 challenge. Furthermore, quantitative acetylome data showed that the K119 site of RELA was deacetylated in fibrotic livers compared to healthy controls. Subsequently, we reveal a new mechanism that SIRT7 deacetylates RELA at the K119 site in largemouth bass. RELA K119 deacetylation enhances RELA transcriptional activity by increasing its DNA-binding activity, and facilitates nuclear translocation of RELA, resulting in the overwhelming release of proinflammatory factors, and subsequently enhancing liver inflammation and fibrosis. Pharmacological inhibition of SIRT7 using a specific inhibitor restores the decreased acetylation of RELA in vivo and in vitro, and reduces the transcriptional activity, nuclear localization of RELA and the expression of its target genes, which ultimately attenuates liver inflammation and fibrosis. These findings uncover a novel mechanism underlying liver fibrosis involving SIRT7-mediated deacetylation of RELA to activate the proinflammatory gene program, and thus provide important insights and biomarkers into the effective strategies for limiting liver inflammation and fibrosis.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00287-9.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 4","pages":"856-875"},"PeriodicalIF":5.3,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662976/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145650040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marinisomatota (formerly recognized as Marinimicrobia, Marine Group A, and SAR406) are ubiquitous and abundant in marine environments, traditionally characterized as heterotrophic microorganisms. However, certain members of Marinisomatota have demonstrated the capacity to harness light for carbon dioxide fixation and the synthesis of organic compounds, thriving in the translucent zone or transitioning between the translucent and aphotic layers. The metabolic strategies driving the shift in trophic behaviors, and the factors influencing these transitions, remain largely unexplored. In this study, we investigate the metabolic strategies, ecological distribution, and dietary patterns of Marinisomatota through the analysis of metagenomic and metatranscriptomic data sourced from the global open oceans. A total of 1,588 Marinisomatota genomes were retrieved, representing one class, two orders, 14 families, 31 genera, and 67 species. These organisms are predominantly found in low-latitude marine regions, with relative abundances ranging from 0.18 to 36.21%. Among the 14 families, S15-B10, TCS55, UBA1611, UBA2128, and UBA8226 exhibit potential for light-dependent processes associated with Crassulacean acid metabolism (M00169). Three distinct metabolic strategies were identified within Marinisomatota: MS0 (photoautotrophic potential), MS1 (heterotrophic with a pronounced glycolytic pathway), and MS2 (heterotrophic without glycolysis). The emergence of these metabolic strategies may be a response to nutrient limitations within the ocean. This study reveals the potential for mixotrophic strategies in Marinisomatota, underscoring the critical interplay between life history traits and metabolic strategies in the evolution of novel nutritional groups.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00293-x.
Marinisomatota(以前被认为是Marinimicrobia, Marine Group A和SAR406)在海洋环境中普遍存在且数量丰富,传统上被认为是异养微生物。然而,Marinisomatota的某些成员已经证明了利用光固定二氧化碳和合成有机化合物的能力,在半透明区或在半透明层和不透明层之间过渡。驱动营养行为转变的代谢策略,以及影响这些转变的因素,在很大程度上仍未被探索。在这项研究中,我们通过分析来自全球开放海洋的元基因组和元转录组数据,研究了Marinisomatota的代谢策略、生态分布和饮食模式。共检索到1纲2目14科31属67种的Marinisomatota基因组1588份。这些生物主要分布在低纬度海域,相对丰度为0.18% ~ 36.21%。在14个家族中,S15-B10、TCS55、UBA1611、UBA2128和UBA8226表现出与天冬氨酸代谢相关的光依赖性过程的潜力(M00169)。在Marinisomatota中确定了三种不同的代谢策略:MS0(光自养电位),MS1(异养具有明显的糖酵解途径)和MS2(异养无糖酵解)。这些代谢策略的出现可能是对海洋中营养限制的一种反应。这项研究揭示了Marinisomatota混合营养策略的潜力,强调了新的营养群体进化中生活史特征和代谢策略之间的关键相互作用。补充信息:在线版本包含补充资料,下载地址为10.1007/s42995-025-00293-x。
{"title":"Ecological diversity and metabolic strategies of widespread Marinisomatota in global oceans.","authors":"Shizheng Xiang, Jianyang Li, Zhen Chen, Ruolin Cheng, Liping Wang, Libo Yu, Guangshan Wei, Xiangyu Guan, Brandon R Briggs, Gary King, Hongchen Jiang, Zongze Shao","doi":"10.1007/s42995-025-00293-x","DOIUrl":"10.1007/s42995-025-00293-x","url":null,"abstract":"<p><p>Marinisomatota (formerly recognized as Marinimicrobia, Marine Group A, and SAR406) are ubiquitous and abundant in marine environments, traditionally characterized as heterotrophic microorganisms. However, certain members of Marinisomatota have demonstrated the capacity to harness light for carbon dioxide fixation and the synthesis of organic compounds, thriving in the translucent zone or transitioning between the translucent and aphotic layers. The metabolic strategies driving the shift in trophic behaviors, and the factors influencing these transitions, remain largely unexplored. In this study, we investigate the metabolic strategies, ecological distribution, and dietary patterns of Marinisomatota through the analysis of metagenomic and metatranscriptomic data sourced from the global open oceans. A total of 1,588 Marinisomatota genomes were retrieved, representing one class, two orders, 14 families, 31 genera, and 67 species. These organisms are predominantly found in low-latitude marine regions, with relative abundances ranging from 0.18 to 36.21%. Among the 14 families, S15-B10, TCS55, UBA1611, UBA2128, and UBA8226 exhibit potential for light-dependent processes associated with Crassulacean acid metabolism (M00169). Three distinct metabolic strategies were identified within Marinisomatota: MS0 (photoautotrophic potential), MS1 (heterotrophic with a pronounced glycolytic pathway), and MS2 (heterotrophic without glycolysis). The emergence of these metabolic strategies may be a response to nutrient limitations within the ocean. This study reveals the potential for mixotrophic strategies in Marinisomatota, underscoring the critical interplay between life history traits and metabolic strategies in the evolution of novel nutritional groups.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00293-x.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 3","pages":"523-536"},"PeriodicalIF":5.3,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12413381/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145016621","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sacoglossan sea slugs have attracted considerable scientific attention due to their capacity to retain functional macroalgal chloroplasts inside their cells. This endosymbiotic association is nutritionally relevant for these organisms and represents an interesting research issue for biotechnological applications. The Caribbean species Elysia crispata can integrate chloroplasts from different macroalgal species. The lipidome of chloroplasts includes lipid classes unique to these photosynthetic organelles. Specialized lipids, such as the glycolipids MGDG, DGDG, and SQDG, are essential for maintaining the integrity of both the thylakoid membranes and the overall chloroplast membrane structure. Additionally, lipids are a diverse group of biomolecules playing essential roles at nutritional and physiological levels. A combined approach using LC-HR-MS and MS/MS was employed to determine the polar lipid profile of the photosynthetic sea slug E. crispata from two habitats in the north-western tropical Atlantic (Sistema Arrecifal Veracruzano and Mahahual) and two different feeding conditions (fed and after 1 week of starvation). Significant differences were identified in the abundance of structural and signalling phospholipids (PC, PI, PG, PS, CL) suggesting different nutritional states between populations. The composition of glycolipids demonstrated a clear separation by habitat, but not by feeding conditions. The lower abundance of glycolipids in the Mahahual samples suggests a lower density of chloroplasts in their tissues compared to Veracruz individuals. These results corroborate that 1 week of starvation is insufficient to initiate the degradation of plastid membranes. This study confirms the advantages of using lipidomics as a tool to enhance our knowledge of the ecology of marine invertebrates.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00281-1.
{"title":"Habitat shapes the lipidome of the tropical photosynthetic sea slug <i>Elysia crispata</i>.","authors":"Felisa Rey, Xochitl Guadalupe Vital, Sónia Cruz, Tânia Melo, Diana Lopes, Ricardo Calado, Nuno Simões, Maite Mascaró, Maria Rosário Domingues","doi":"10.1007/s42995-025-00281-1","DOIUrl":"10.1007/s42995-025-00281-1","url":null,"abstract":"<p><p>Sacoglossan sea slugs have attracted considerable scientific attention due to their capacity to retain functional macroalgal chloroplasts inside their cells. This endosymbiotic association is nutritionally relevant for these organisms and represents an interesting research issue for biotechnological applications. The Caribbean species <i>Elysia crispata</i> can integrate chloroplasts from different macroalgal species. The lipidome of chloroplasts includes lipid classes unique to these photosynthetic organelles. Specialized lipids, such as the glycolipids MGDG, DGDG, and SQDG, are essential for maintaining the integrity of both the thylakoid membranes and the overall chloroplast membrane structure. Additionally, lipids are a diverse group of biomolecules playing essential roles at nutritional and physiological levels. A combined approach using LC-HR-MS and MS/MS was employed to determine the polar lipid profile of the photosynthetic sea slug <i>E. crispata</i> from two habitats in the north-western tropical Atlantic (Sistema Arrecifal Veracruzano and Mahahual) and two different feeding conditions (fed and after 1 week of starvation). Significant differences were identified in the abundance of structural and signalling phospholipids (PC, PI, PG, PS, CL) suggesting different nutritional states between populations. The composition of glycolipids demonstrated a clear separation by habitat, but not by feeding conditions. The lower abundance of glycolipids in the Mahahual samples suggests a lower density of chloroplasts in their tissues compared to Veracruz individuals. These results corroborate that 1 week of starvation is insufficient to initiate the degradation of plastid membranes. This study confirms the advantages of using lipidomics as a tool to enhance our knowledge of the ecology of marine invertebrates.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00281-1.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 2","pages":"382-396"},"PeriodicalIF":5.8,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102446/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144144488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}