{"title":"羔羊卵巢和卵母细胞转录组学特征揭示了超排卵后的关键生物标志物。","authors":"Jingjing Wang, Jiachen Bai, Yucheng Liu, Zhenliang Zhang, Zhanmin Lv, Guiping Hai, Houru Li, Weijun Liu, Ling Tang, Yuxuan Hua, Ruigang Wang, Yunyun Zhang, Xiangwei Fu, Pengcheng Wan","doi":"10.1093/jas/skaf193","DOIUrl":null,"url":null,"abstract":"<p><p>Superovulated prepubertal lambs serve as an important source of oocytes for Juvenile In Vitro Embryo Transfer (JIVET); however, their ovarian response to gonadotropin stimulation markedly differs from that of adult ewes. The ovaries and oocytes are the primary targets of hormonal-induced superovulation in lambs, and their developmental status directly determines the efficiency of follicular recruitment and maturation. In this study, the in vitro developmental assessment revealed that the maturation rate, cleavage rate, and blastocyst formation rate of lamb oocytes were significantly lower (P < 0.05) than those of adult sheep oocytes. To investigate this disparity, whole transcriptome sequencing (RNA-seq) of ovaries and ultra-low RNA-seq of oocytes collected from adult sheep and lamb were performed. Integrative transcriptomic analysis identified a significant enrichment of differentially expressed genes (DEGs) in the PI3K/Akt signaling pathway across ovarian and oocytes. Both Immunofluorescence and Immunohistochemistry analyses revealed key nodes ERBB3, HRAS proteins in this pathway exhibited elevated expression in both ovarian follicles and oocytes of superovulated lambs. Collectively, ERBB3 and HRAS serve as key biomarkers for the reduced developmental competence of oocytes in lambs following superovulation.</p>","PeriodicalId":14895,"journal":{"name":"Journal of animal science","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transcriptomic characterization of lamb ovaries and oocytes reveals key biomarkers after superovulation.\",\"authors\":\"Jingjing Wang, Jiachen Bai, Yucheng Liu, Zhenliang Zhang, Zhanmin Lv, Guiping Hai, Houru Li, Weijun Liu, Ling Tang, Yuxuan Hua, Ruigang Wang, Yunyun Zhang, Xiangwei Fu, Pengcheng Wan\",\"doi\":\"10.1093/jas/skaf193\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Superovulated prepubertal lambs serve as an important source of oocytes for Juvenile In Vitro Embryo Transfer (JIVET); however, their ovarian response to gonadotropin stimulation markedly differs from that of adult ewes. The ovaries and oocytes are the primary targets of hormonal-induced superovulation in lambs, and their developmental status directly determines the efficiency of follicular recruitment and maturation. In this study, the in vitro developmental assessment revealed that the maturation rate, cleavage rate, and blastocyst formation rate of lamb oocytes were significantly lower (P < 0.05) than those of adult sheep oocytes. To investigate this disparity, whole transcriptome sequencing (RNA-seq) of ovaries and ultra-low RNA-seq of oocytes collected from adult sheep and lamb were performed. Integrative transcriptomic analysis identified a significant enrichment of differentially expressed genes (DEGs) in the PI3K/Akt signaling pathway across ovarian and oocytes. Both Immunofluorescence and Immunohistochemistry analyses revealed key nodes ERBB3, HRAS proteins in this pathway exhibited elevated expression in both ovarian follicles and oocytes of superovulated lambs. Collectively, ERBB3 and HRAS serve as key biomarkers for the reduced developmental competence of oocytes in lambs following superovulation.</p>\",\"PeriodicalId\":14895,\"journal\":{\"name\":\"Journal of animal science\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-06-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of animal science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1093/jas/skaf193\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of animal science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/jas/skaf193","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Transcriptomic characterization of lamb ovaries and oocytes reveals key biomarkers after superovulation.
Superovulated prepubertal lambs serve as an important source of oocytes for Juvenile In Vitro Embryo Transfer (JIVET); however, their ovarian response to gonadotropin stimulation markedly differs from that of adult ewes. The ovaries and oocytes are the primary targets of hormonal-induced superovulation in lambs, and their developmental status directly determines the efficiency of follicular recruitment and maturation. In this study, the in vitro developmental assessment revealed that the maturation rate, cleavage rate, and blastocyst formation rate of lamb oocytes were significantly lower (P < 0.05) than those of adult sheep oocytes. To investigate this disparity, whole transcriptome sequencing (RNA-seq) of ovaries and ultra-low RNA-seq of oocytes collected from adult sheep and lamb were performed. Integrative transcriptomic analysis identified a significant enrichment of differentially expressed genes (DEGs) in the PI3K/Akt signaling pathway across ovarian and oocytes. Both Immunofluorescence and Immunohistochemistry analyses revealed key nodes ERBB3, HRAS proteins in this pathway exhibited elevated expression in both ovarian follicles and oocytes of superovulated lambs. Collectively, ERBB3 and HRAS serve as key biomarkers for the reduced developmental competence of oocytes in lambs following superovulation.
期刊介绍:
The Journal of Animal Science (JAS) is the premier journal for animal science and serves as the leading source of new knowledge and perspective in this area. JAS publishes more than 500 fully reviewed research articles, invited reviews, technical notes, and letters to the editor each year.
Articles published in JAS encompass a broad range of research topics in animal production and fundamental aspects of genetics, nutrition, physiology, and preparation and utilization of animal products. Articles typically report research with beef cattle, companion animals, goats, horses, pigs, and sheep; however, studies involving other farm animals, aquatic and wildlife species, and laboratory animal species that address fundamental questions related to livestock and companion animal biology will be considered for publication.