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中华蜜蜂6日龄幼虫响应蜜蜂球囊菌侵染的长链非编码RNA应答研究
引用本文:杜宇,冯睿蓉,王杰,祝智威,张文德,余岢骏,隆琦,蔡宗兵,解彦玲,熊翠玲,郑燕珍,陈大福,郭睿. 中华蜜蜂6日龄幼虫响应蜜蜂球囊菌侵染的长链非编码RNA应答研究[J]. 微生物学报, 2021, 61(5): 1338-1358
作者姓名:杜宇  冯睿蓉  王杰  祝智威  张文德  余岢骏  隆琦  蔡宗兵  解彦玲  熊翠玲  郑燕珍  陈大福  郭睿
作者单位:福建农林大学动物科学学院(蜂学学院), 福建 福州 350002;福建农林大学动物科学学院(蜂学学院), 福建 福州 350002;福建农林大学蜂产品加工与应用教育部工程研究中心, 福建 福州 350002
基金项目:国家自然科学基金(31702190);国家现代农业产业技术体系建设专项资金(CARS-44-KXJ7);福建省教育厅中青年教师教育科研项目(JAT170158);福建农林大学科技创新专项基金(CXZX2017342,CXZX2017343);福建农林大学硕士生导师团队项目(郭睿);福建省病原真菌与真菌毒素重点实验室开放课题;福建农林大学优秀硕士学位论文资助基金(杜宇)
摘    要:[目的]本研究旨在探究长链非编码RNA (long non-coding RNA,lncRNA)在中华蜜蜂(Apis cerana cerana,简称中蜂)6日龄幼虫应答蜜蜂球囊菌(Ascosphaera apis,简称球囊菌)侵染过程中的差异表达谱及调控作用.[方法]利用链特异性cDNA建库的RNA-seq技术对未被...

关 键 词:中华蜜蜂  幼虫  蜜蜂球囊菌  长链非编码RNA  竞争性内源RNA  免疫应答
收稿时间:2020-07-10
修稿时间:2020-10-05

Long non-coding RNA response of 6-day-old Apis cerana cerana larvae to Ascosphaera apis infection
Yu Du,Ruirong Feng,Jie Wang,Zhiwei Zhu,Wende Zhang,Kejun Yu,Qi Long,Zongbing Cai,Yanling Xie,Cuiling Xiong,Yanzhen Zheng,Dafu Chen,Rui Guo. Long non-coding RNA response of 6-day-old Apis cerana cerana larvae to Ascosphaera apis infection[J]. Acta microbiologica Sinica, 2021, 61(5): 1338-1358
Authors:Yu Du  Ruirong Feng  Jie Wang  Zhiwei Zhu  Wende Zhang  Kejun Yu  Qi Long  Zongbing Cai  Yanling Xie  Cuiling Xiong  Yanzhen Zheng  Dafu Chen  Rui Guo
Affiliation:College of Animal Sciences(College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian Province, China;College of Animal Sciences(College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian Province, China;Engineering Research Center of Processing and Application of Bee Products of Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian Province, China
Abstract:[Objective] This study aims to investigate the differential expression pattern of long non-coding RNAs (lncRNAs) and their regulatory function involved in Apis cerana cerana 6-day-old larval gut response to Ascosphaera apis infection. [Methods] Un-infected and Ascosphaera apis-infected 6-day-old larval guts of Apis cerana cerana (AcCK and AcT) were sequenced using strand-specific cDNA library-based RNA-seq technology. Structural characteristics and expression pattern of lncRNAs were analyzed using related bioinformatic softwares. DElncRNAs were screened followed by investigation of their cis-acting role and competitive endogenous RNA (ceRNA) network. RT-qPCR was conducted to verify the sequencing data and expression pattern of DElncRNAs. [Results] Here, 642 known lncRNAs and 487 novel lncRNAs were identified. Compared with mRNAs, these Apis cerana cerana lncRNAs were shorter in exon and intron length, fewer in exon number and lower in expression level. Additionally, 43 antisense lncRNAs were discovered to have complementary relationship with 40 sense-strand mRNAs. In AcCK vs. AcT comparison group, 367 up-regulated lncRNAs and 268 down-regulated ones were identified. In total, 194 DElncRNAs were found to potentially regulate 461 upstream and downstream genes, which were annotated to 38 functional terms such as cellular process, metabolic process and catalytic activity, as well as 191 pathways including amino acid metabolism, endocytosis and MAPK signaling pathways. Moreover, 180 DElncRNAs can target 50 DEmiRNAs, further regulating 6365 mRNAs; additionally, complex regulatory networks existed among them. [Conclusion] These results demonstrated that partial antisense lncRNAs may participate in host response to Ascosphaera apis infection; some DElncRNAs may regulate upstream and downstream genes relative to material metabolism and immune-associated pathways, thus mediating host Ascosphaera apis-response; a portion of DElncRNAs including TCONS_00010661 and TCONS_00003104 were likely to regulate Jak-STAT signaling pathway and oxidative phosphorylation and corresponding enriched genes via ceRNA networks, further participating in the response of host to Ascosphaera apis invasion.
Keywords:Apis cerana cerana  larva  Ascosphaera apis  long non-coding RNA  competitive endogenous RNA  immune response
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