4.7 Article

Circular RNAs Repertoire and Expression Profile during Brassica rapa Pollen Development

Journal

Publisher

MDPI
DOI: 10.3390/ijms221910297

Keywords

Brassica rapa; circRNAs; pollen development; RNA sequencing

Funding

  1. University of Melbourne Research Scholarship
  2. ARC [DP0988972]
  3. Australian Research Council [DP0988972] Funding Source: Australian Research Council

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This study investigated the expression profile and potential function of circRNAs during pollen development in Brassica rapa through high-throughput RNA sequencing. Functional enrichment analysis revealed circRNAs' involvement in pollen-related molecular and biological processes, indicating their potential role in post-transcriptional gene regulation.Confirmation of back-splicing sites of selected circRNAs further supports the systematic analysis of circRNAs during pollen development for future studies on gene regulatory networks in flowering plants.
Circular RNAs (circRNAs) are covalently closed RNA molecules generated by the back-splicing of exons from linear precursor mRNAs. Though various linear RNAs have been shown to play important regulatory roles in many biological and developmental processes, little is known about the role of their circular counterparts. In this study, we performed high-throughput RNA sequencing to delineate the expression profile and potential function of circRNAs during the five stages of pollen development in Brassica rapa. A total of 1180 circRNAs were detected in pollen development, of which 367 showed stage-specific expression patterns. Functional enrichment and metabolic pathway analysis showed that the parent genes of circRNAs were mainly involved in pollen-related molecular and biological processes such as mitotic and meiotic cell division, DNA processes, protein synthesis, protein modification, and polysaccharide biosynthesis. Moreover, by predicting the circRNA-miRNA network from our differentially expressed circRNAs, we found 88 circRNAs with potential miRNA binding sites, suggesting their role in post-transcriptional regulation of the genes. Finally, we confirmed the back-splicing sites of nine selected circRNAs using divergent primers and Sanger sequencing. Our study presents the systematic analysis of circular RNAs during pollen development and forms the basis of future studies for unlocking complex gene regulatory networks underpinning reproduction in flowering plants.

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