Identification of long non-coding RNAs and microRNAs involved in anther development in the tropical Camellia oleifera

被引:5
作者
Kong, Lingshan [1 ,2 ,3 ]
Zhuo, Yanjing [4 ]
Xu, Jieru [1 ,2 ]
Meng, Xiangxu [1 ,2 ]
Wang, Yue [1 ,2 ]
Zhao, Wenxiu [1 ,2 ]
Lai, Hanggui [5 ]
Chen, Jinhui [1 ,2 ]
Wang, Jian [1 ,3 ]
机构
[1] Hainan Univ, Hainan Yazhou Bay Seed Lab, Sanya Nanfan Res Inst, Sanya 572025, Peoples R China
[2] Hainan Univ, Key Lab Genet & Germplasm Innovat Trop Special Fo, Sch Forestry, Minist Educ,Engn Res Ctr Rare & Precious Tree Spe, Haikou 570228, Hainan, Peoples R China
[3] Hainan Univ, Sch Hort, Haikou 570228, Hainan, Peoples R China
[4] Hainan Univ, Sch Publ Adm, Haikou 570228, Hainan, Peoples R China
[5] Hainan Univ, Sch Trop Crops, Haikou 570228, Hainan, Peoples R China
关键词
Anther development; MicroRNAs; Long non-coding RNAs; Network; Camellia oleifera; GENOME-WIDE IDENTIFICATION; ARABIDOPSIS-THALIANA; POLLEN DEVELOPMENT; MALE-FERTILITY; SPOROPOLLENIN SYNTHESIS; FLOWER DEVELOPMENT; EXINE FORMATION; EVOLUTION; DATABASE; PATHWAY;
D O I
10.1186/s12864-022-08836-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Explored the molecular science of anther development is important for improving productivity and overall yield of crops. Although the role of regulatory RNAs, including long non-coding RNAs (lncRNAs) and microRNAs (miRNAs), in regulating anther development has been established, their identities and functions in Camellia oleifera, an important industrial crop, have yet not been clearly explored. Here, we report the identification and characterization of genes, lncRNAs and miRNAs during three stages of the tropical C. oleifera anther development by single-molecule real-time sequencing, RNA sequencing and small RNA sequencing, respectively. Results These stages, viz. the pollen mother cells stage, tetrad stage and uninucleate pollen stage, were identified by analyzing paraffin sections of floral buds during rapid expansion periods. A total of 18,393 transcripts, 414 putative lncRNAs and 372 miRNAs were identified, of which 5,324 genes, 115 lncRNAs, and 44 miRNAs were differentially accumulated across three developmental stages. Of these, 44 and 92 genes were predicted be regulated by 37 and 30 differentially accumulated lncRNAs and miRNAs, respectively. Additionally, 42 differentially accumulated lncRNAs were predicted as targets of 27 miRNAs. Gene ontology enrichment indicated that potential target genes of lncRNAs were enriched in photosystem II, regulation of autophagy and carbohydrate phosphatase activity, which are essential for anther development. Functional annotation of genes targeted by miRNAs indicated that they are relevant to transcription and metabolic processes that play important roles in microspore development. An interaction network was built with 2 lncRNAs, 6 miRNAs and 10 mRNAs. Among these, miR396 and miR156 family were up-regulated, while their targets, genes (GROWTH REGULATING FACTORS and SQUAMOSA PROMOTER BINDING PROTEIN-LIKE genes) and lncRNAs, were down-regulated. Further, the trans-regulated targets of these lncRNAs, like wall-associated kinase2 and phosphomannose isomerase1, are involved in pollen wall formation during anther development. Conclusions This study unravels lncRNAs, miRNAs and miRNA-lncRNA-mRNA networks involved in development of anthers of the tropical C. oleifera lays a theoretical foundation for further elucidation of regulatory roles of lncRNAs and miRNAs in anther development.
引用
收藏
页数:18
相关论文
共 109 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Two-tailed RT-qPCR: a novel method for highly accurate miRNA quantification [J].
Androvic, Peter ;
Valihrach, Lukas ;
Elling, Julie ;
Sjoback, Robert ;
Kubista, Mikael .
NUCLEIC ACIDS RESEARCH, 2017, 45 (15)
[3]  
Arrieta M, 2020, METHODS MOL BIOL, V2061, P367, DOI 10.1007/978-1-4939-9818-0_26
[4]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[5]   MicroRNA156 as a promising tool for alfalfa improvement [J].
Aung, Banyar ;
Gruber, Margaret Y. ;
Amyot, Lisa ;
Omari, Khaled ;
Bertrand, Annick ;
Hannoufa, Abdelali .
PLANT BIOTECHNOLOGY JOURNAL, 2015, 13 (06) :779-790
[6]   RNA regulatory networks in animals and plants: a long noncoding RNA perspective [J].
Bai, Youhuang ;
Dai, Xiaozhuan ;
Harrison, Andrew P. ;
Chen, Ming .
BRIEFINGS IN FUNCTIONAL GENOMICS, 2015, 14 (02) :91-101
[7]   The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000 [J].
Bairoch, A ;
Apweiler, R .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :45-48
[8]   Barley Anther and Meiocyte Transcriptome Dynamics in Meiotic Prophase I [J].
Barakate, Abdellah ;
Orr, Jamie ;
Schreiber, Miriam ;
Colas, Isabelle ;
Lewandowska, Dominika ;
McCallum, Nicola ;
Macaulay, Malcolm ;
Morris, Jenny ;
Arrieta, Mikel ;
Hedley, Pete E. ;
Ramsay, Luke ;
Waugh, Robbie .
FRONTIERS IN PLANT SCIENCE, 2021, 11
[9]   A role for the miR396/GRF network in specification of organ type during flower development, as supported by ectopic expression of Populus trichocarpa miR396c in transgenic tobacco [J].
Baucher, M. ;
Moussawi, J. ;
Vandeputte, O. M. ;
Monteyne, D. ;
Mol, A. ;
Perez-Morga, D. ;
El Jaziri, M. .
PLANT BIOLOGY, 2013, 15 (05) :892-898
[10]   Transcript profiling of Populus tomentosa genes in normal, tension, and opposite wood by RNA-seq [J].
Chen, Jinhui ;
Chen, Beibei ;
Zhang, Deqiang .
BMC GENOMICS, 2015, 16