Abstract

Alternative splicing (AS) is a post-transcriptional process common in plants and essential for regulation of environmental fitness of plants. In the present study, we focus on the AS events in poplar leaves to understand their effects on plant growth and development. The hybrid poplar (P.alba×P.glandulosa cv.84K) leaves were collected for RNA extraction. The extracted RNA was sequenced using on an Illumina HiSeq™ 2000 platform. Using the Populus trichocarpa genome as the reference, a total of 3810 AS genes were identified (9225 AS events), which accounted for 13.51% of all the expressed genes. Intron retention was the most common AS event, accounting for 43.86% of all the AS events, followed by alternative 3' splice sites (23.75%), alternative 5' splice sites (23.71%), and exon skipping (8.68%). Chromosomes 10 had the most condensed AS events (33.67 events/Mb) and chromosome 19 had the least (12.42 events/Mb). Association analysis showed that AS in the poplar leaves was positively correlated with intron length, exon number, exon length, and gene expression level, and was negatively correlated with GC content. AS genes in the poplar leaves were associated mainly with inositol phosphate metabolism and phosphatidylinositol signaling system pathways that would be significant on wooden plant production.

Highlights

  • Most plant genes contain introns with conserved nucleotides (GT-AG) at both ends

  • The number of reads mapped to the reference genome accounted for 68.27% of the total clean reads; 65.94% were uniquely aligned and the remaining 2.33% mapped to multiple loci

  • The results showed that all six genes each had two transcripts in the poplar leaves (Fig 1)

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Summary

Introduction

Most plant genes contain introns with conserved nucleotides (GT-AG) at both ends. The initial transcription product, pre-RNA, is spliced to remove introns and the remaining exons are ligated to form mature coding mRNA sequences. Accurate splicing of gene transcripts is essential for the growth and development of plants and is helpful for their adaptation to variable environment conditions [1]. The pre-mRNA sequences can undergo alternative splicing (AS) to produce different splicing isoforms. The circadian clock associated gene CCA1 in Arabidopsis had two AS products, a full-size CCA1α isoform and an incomplete CCA1β isoform in which the MYB DNA-binding motif is missing [2].

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