Yan-Hua Chen, Tao Jiang, Ayinuer Yasen, Bing-Yan Fan, Juan Zhu, Mei-Xian Wang, Xing-Jia Shen
{"title":"RNA <i>N6-</i>methyladenosine of <i>DHAPAT</i> and <i>PAP</i> involves in regulation of diapause of <i>Bombyx mori</i> via the lipid metabolism pathway.","authors":"Yan-Hua Chen, Tao Jiang, Ayinuer Yasen, Bing-Yan Fan, Juan Zhu, Mei-Xian Wang, Xing-Jia Shen","doi":"10.1017/S0007485323000330","DOIUrl":null,"url":null,"abstract":"<p><p>Environment-induced epigenetics are involved in diapause regulation, but the molecular mechanism that epigenetically couples nutrient metabolism to diapause regulation remains unclear. In this study, we paid special attention to the significant differences in the level of <i>N6</i>-adenosine methylation (m<sup>6</sup>A) of dihydroxyacetone phosphate acyltransferase (<i>DHAPAT</i>) and phosphatidate phosphatase (<i>PAP</i>) genes in the lipid metabolism pathway of the bivoltine silkworm (<i>Bombyx mori</i>) strain Qiufeng developed from eggs incubated at a normal temperature (QFHT, diapause egg producer) compared to those from eggs incubated at a low temperature (QFLT, non-diapause egg producer). We knocked down <i>DHAPAT</i> in the pupal stage of the QFLT group, resulting in the non-diapause destined eggs becoming diapausing eggs. In the <i>PAP</i> knockdown group, the colour of the non-diapause destined eggs changed from light yellow to pink 3 days after oviposition, but they hatched as normal. Moreover, we validated that YTHDF3 binds to m<sup>6</sup>A-modified <i>DHAPAT</i> and <i>PAP</i> mRNAs to promote their stability and translation. These results suggest that RNA m<sup>6</sup>A methylation participates in the diapause regulation of silkworm by changing the expression levels of <i>DHAPAT</i> and <i>PAP</i> and reveal that m<sup>6</sup>A epigenetic modification can be combined with a lipid metabolism signal pathway to participate in the regulation of insect diapause traits, which provides a clearer image for exploring the physiological basis of insect diapause.</p>","PeriodicalId":9370,"journal":{"name":"Bulletin of Entomological Research","volume":null,"pages":null},"PeriodicalIF":1.6000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Entomological Research","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1017/S0007485323000330","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/8/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Environment-induced epigenetics are involved in diapause regulation, but the molecular mechanism that epigenetically couples nutrient metabolism to diapause regulation remains unclear. In this study, we paid special attention to the significant differences in the level of N6-adenosine methylation (m6A) of dihydroxyacetone phosphate acyltransferase (DHAPAT) and phosphatidate phosphatase (PAP) genes in the lipid metabolism pathway of the bivoltine silkworm (Bombyx mori) strain Qiufeng developed from eggs incubated at a normal temperature (QFHT, diapause egg producer) compared to those from eggs incubated at a low temperature (QFLT, non-diapause egg producer). We knocked down DHAPAT in the pupal stage of the QFLT group, resulting in the non-diapause destined eggs becoming diapausing eggs. In the PAP knockdown group, the colour of the non-diapause destined eggs changed from light yellow to pink 3 days after oviposition, but they hatched as normal. Moreover, we validated that YTHDF3 binds to m6A-modified DHAPAT and PAP mRNAs to promote their stability and translation. These results suggest that RNA m6A methylation participates in the diapause regulation of silkworm by changing the expression levels of DHAPAT and PAP and reveal that m6A epigenetic modification can be combined with a lipid metabolism signal pathway to participate in the regulation of insect diapause traits, which provides a clearer image for exploring the physiological basis of insect diapause.
期刊介绍:
Established in 1910, the internationally recognised Bulletin of Entomological Research aims to further global knowledge of entomology through the generalisation of research findings rather than providing more entomological exceptions. The Bulletin publishes high quality and original research papers, ''critiques'' and review articles concerning insects or other arthropods of economic importance in agriculture, forestry, stored products, biological control, medicine, animal health and natural resource management. The scope of papers addresses the biology, ecology, behaviour, physiology and systematics of individuals and populations, with a particular emphasis upon the major current and emerging pests of agriculture, horticulture and forestry, and vectors of human and animal diseases. This includes the interactions between species (plants, hosts for parasites, natural enemies and whole communities), novel methodological developments, including molecular biology, in an applied context. The Bulletin does not publish the results of pesticide testing or traditional taxonomic revisions.