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Comprehensive Identification and Analysis of CircRNAs During Hickory ( Sarg.) Flower Bud Differentiation

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Journal Front Plant Sci
Date 2023 Jan 23
PMID 36684801
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Abstract

Flower bud differentiation represents a crucial transition from vegetative growth to reproductive development. (hickory) is an important economic species in China, with a long juvenile period that hinders its commercial development. In recent years, circular RNAs (circRNAs) have been widely studied and identified as sponges for miRNA regulation of mRNA expression. However, little is known regarding the role of circRNAs in flower buds. In this study, we sequenced circRNAs at three developmental stages (undifferentiated, differentiating, and fully differentiated) in both female and male buds. A total of 6,931 circRNAs were identified in the three developmental stages and 4,449 and 2,209 circRNAs were differentially expressed in female and male buds, respectively. Gene ontology demonstrated that many circRNA host genes participated in various processes, for example, cellular and intracellular pH regulation. Function annotation identified 46 differentially expressed circRNAs involved in flowering regulation, with 28 circRNAs found only in female buds, 4 found only in male buds, and 11 found in both female and male buds. A circRNA-miRNA-mRNA network was predicted based on 13 flowering-related circRNAs and their seven putative interacting miRNAs to describe the regulatory mechanism. Our preliminary results demonstrated a potential involvement of circRNA in bud differentiation. They provided a preliminary theoretical basis for how circRNA might participate in flower development in hickory, perhaps in woody plants.

Citing Articles

Advances in CircRNAs in the Past Decade: Review of CircRNAs Biogenesis, Regulatory Mechanisms, and Functions in Plants.

Zhang D, Ma Y, Naz M, Ahmed N, Zhang L, Zhou J Genes (Basel). 2024; 15(7).

PMID: 39062737 PMC: 11276256. DOI: 10.3390/genes15070958.

References
1.
Heo J, Sung S . Vernalization-mediated epigenetic silencing by a long intronic noncoding RNA. Science. 2010; 331(6013):76-9. DOI: 10.1126/science.1197349. View

2.
Chekanova J . Long non-coding RNAs and their functions in plants. Curr Opin Plant Biol. 2015; 27:207-16. DOI: 10.1016/j.pbi.2015.08.003. View

3.
Zhang F, Zhang R, Zhang X, Wu Y, Li X, Zhang S . Comprehensive analysis of circRNA expression pattern and circRNA-miRNA-mRNA network in the pathogenesis of atherosclerosis in rabbits. Aging (Albany NY). 2018; 10(9):2266-2283. PMC: 6188486. DOI: 10.18632/aging.101541. View

4.
Wang D, Gao Y, Sun S, Li L, Wang K . Expression Characteristics in Roots, Phloem, Leaves, Flowers and Fruits of Apple circRNA. Genes (Basel). 2022; 13(4). PMC: 9030095. DOI: 10.3390/genes13040712. View

5.
Xu K, Chen D, Wang Z, Ma J, Zhou J, Chen N . Annotation and functional clustering of circRNA expression in rhesus macaque brain during aging. Cell Discov. 2018; 4:48. PMC: 6141548. DOI: 10.1038/s41421-018-0050-1. View