Longhao Tang , Xiangyi Wei , Liying Zhang , Zhidan Peng , Zulian Liu , Yongping Huang , Pinhua Rao , Lili Yan , Dehong Yang
{"title":"BmLid具有组蛋白赖氨酸去甲基化酶活性,并调节家蚕的卵发生。","authors":"Longhao Tang , Xiangyi Wei , Liying Zhang , Zhidan Peng , Zulian Liu , Yongping Huang , Pinhua Rao , Lili Yan , Dehong Yang","doi":"10.1016/j.ibmb.2025.104359","DOIUrl":null,"url":null,"abstract":"<div><div>Lepidoptera, a major threat to global agriculture, possesses robust reproductive strategies, making understanding reproduction crucial for developing sterile insect techniques (SIT). The silkworm (<em>Bombyx mori</em>), a model lepidopteran, exhibits polytrophic meroistic oogenesis involving trophocyte-mediated nutrient transport and vitellogenin receptor (VgR)-dependent yolk protein uptake. However, epigenetic regulation of these processes remains unclear. This study investigates the role of <em>BmLid</em>, a histone demethylase, in silkworm oogenesis. Using CRISPR/Cas9, we generated <em>BmLid</em> knockout mutants (Δ<em>BmLid</em>) and confirmed gene disruption via sequencing and western blotting. Δ<em>BmLid</em> females exhibited developmental defects and complete sterility, despite unaffected mating behavior or sperm migration. The H3K4me2/me3 and H3K9me2/me3 levels were significantly increased in Δ<em>BmLid</em> ovaries, indicating <em>BmLid</em> has broad demethylase activity <em>in vivo,</em> too. Transcriptomic analysis showed significant downregulation of <em>VgR</em>, critical for vitellogenin transport, alongside dysregulation of cell junction and apoptosis pathways. These defects disrupted follicular epithelium integrity and yolk protein deposition, mirroring similar phenotypes observed in <em>VgR</em> mutants. Our findings demonstrate that <em>BmLid</em> regulates oogenesis by modulating histone methylation to control <em>VgR</em> expression, cell adhesion, and cell apoptosis, thereby ensuring vitellogenesis. This study highlights epigenetic mechanisms underlying lepidopteran reproduction and identifies <em>BmLid</em> as a potential target for SIT-based pest management strategies.</div></div>","PeriodicalId":330,"journal":{"name":"Insect Biochemistry and Molecular Biology","volume":"183 ","pages":"Article 104359"},"PeriodicalIF":3.7000,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"BmLid has histone lysine demethylase activity and regulates oogenesis in the silkworm, Bombyx mori\",\"authors\":\"Longhao Tang , Xiangyi Wei , Liying Zhang , Zhidan Peng , Zulian Liu , Yongping Huang , Pinhua Rao , Lili Yan , Dehong Yang\",\"doi\":\"10.1016/j.ibmb.2025.104359\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Lepidoptera, a major threat to global agriculture, possesses robust reproductive strategies, making understanding reproduction crucial for developing sterile insect techniques (SIT). The silkworm (<em>Bombyx mori</em>), a model lepidopteran, exhibits polytrophic meroistic oogenesis involving trophocyte-mediated nutrient transport and vitellogenin receptor (VgR)-dependent yolk protein uptake. However, epigenetic regulation of these processes remains unclear. This study investigates the role of <em>BmLid</em>, a histone demethylase, in silkworm oogenesis. Using CRISPR/Cas9, we generated <em>BmLid</em> knockout mutants (Δ<em>BmLid</em>) and confirmed gene disruption via sequencing and western blotting. Δ<em>BmLid</em> females exhibited developmental defects and complete sterility, despite unaffected mating behavior or sperm migration. The H3K4me2/me3 and H3K9me2/me3 levels were significantly increased in Δ<em>BmLid</em> ovaries, indicating <em>BmLid</em> has broad demethylase activity <em>in vivo,</em> too. Transcriptomic analysis showed significant downregulation of <em>VgR</em>, critical for vitellogenin transport, alongside dysregulation of cell junction and apoptosis pathways. These defects disrupted follicular epithelium integrity and yolk protein deposition, mirroring similar phenotypes observed in <em>VgR</em> mutants. Our findings demonstrate that <em>BmLid</em> regulates oogenesis by modulating histone methylation to control <em>VgR</em> expression, cell adhesion, and cell apoptosis, thereby ensuring vitellogenesis. This study highlights epigenetic mechanisms underlying lepidopteran reproduction and identifies <em>BmLid</em> as a potential target for SIT-based pest management strategies.</div></div>\",\"PeriodicalId\":330,\"journal\":{\"name\":\"Insect Biochemistry and Molecular Biology\",\"volume\":\"183 \",\"pages\":\"Article 104359\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-07-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Insect Biochemistry and Molecular Biology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0965174825001031\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Biochemistry and Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0965174825001031","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
BmLid has histone lysine demethylase activity and regulates oogenesis in the silkworm, Bombyx mori
Lepidoptera, a major threat to global agriculture, possesses robust reproductive strategies, making understanding reproduction crucial for developing sterile insect techniques (SIT). The silkworm (Bombyx mori), a model lepidopteran, exhibits polytrophic meroistic oogenesis involving trophocyte-mediated nutrient transport and vitellogenin receptor (VgR)-dependent yolk protein uptake. However, epigenetic regulation of these processes remains unclear. This study investigates the role of BmLid, a histone demethylase, in silkworm oogenesis. Using CRISPR/Cas9, we generated BmLid knockout mutants (ΔBmLid) and confirmed gene disruption via sequencing and western blotting. ΔBmLid females exhibited developmental defects and complete sterility, despite unaffected mating behavior or sperm migration. The H3K4me2/me3 and H3K9me2/me3 levels were significantly increased in ΔBmLid ovaries, indicating BmLid has broad demethylase activity in vivo, too. Transcriptomic analysis showed significant downregulation of VgR, critical for vitellogenin transport, alongside dysregulation of cell junction and apoptosis pathways. These defects disrupted follicular epithelium integrity and yolk protein deposition, mirroring similar phenotypes observed in VgR mutants. Our findings demonstrate that BmLid regulates oogenesis by modulating histone methylation to control VgR expression, cell adhesion, and cell apoptosis, thereby ensuring vitellogenesis. This study highlights epigenetic mechanisms underlying lepidopteran reproduction and identifies BmLid as a potential target for SIT-based pest management strategies.
期刊介绍:
This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.