National Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian, 271018, China.
Departments of Botany and Genetics, University of Wisconsin-Madison, Madison, 53706, USA.
Plant J. 2019 May;98(4):714-726. doi: 10.1111/tpj.14268. Epub 2019 Mar 25.
Pre-mRNA splicing is an important step for gene expression regulation. Yeast Bud13p (bud-site selection protein 13) regulates the budding pattern and pre-mRNA splicing in yeast cells; however, no Bud13p homologs have been identified in plants. Here, we isolated two mutants that carry T-DNA insertions at the At1g31870 locus and shows early embryo lethality and seed abortion. At1g31870 encodes an Arabidopsis homolog of yeast Bud13p, AtBUD13. Although AtBUD13 homologs are widely distributed in eukaryotic organisms, phylogenetic analysis revealed that their protein domain organization is more complex in multicellular species. AtBUD13 is expressed throughout plant development including embryogenesis and AtBUD13 proteins is localized in the nucleus in Arabidopsis. RNA-seq analysis revealed that AtBUD13 mutation predominantly results in the intron retention, especially for shorter introns (≤100 bases). Within this group of genes, we identified 52 genes involved in embryogenesis, out of which 22 are involved in nucleic acid metabolism. Our results demonstrate that AtBUD13 plays critical roles in early embryo development by effecting pre-mRNA splicing.
前体 mRNA 剪接是基因表达调控的重要步骤。酵母 Bud13p(芽位点选择蛋白 13)调节酵母细胞的出芽模式和前体 mRNA 剪接;然而,在植物中尚未鉴定出 Bud13p 的同源物。在这里,我们分离到两个携带 T-DNA 插入 At1g31870 基因座的突变体,表现出早期胚胎致死和种子败育。At1g31870 编码酵母 Bud13p 的拟南芥同源物 AtBUD13。尽管 AtBUD13 同源物在真核生物中广泛分布,但系统发育分析表明,它们的蛋白结构域组织在多细胞物种中更为复杂。AtBUD13 在植物发育的整个过程中表达,包括胚胎发生,并且 AtBUD13 蛋白在拟南芥中定位于细胞核。RNA-seq 分析表明,AtBUD13 突变主要导致内含子保留,尤其是较短的内含子(≤100 个碱基)。在这群基因中,我们鉴定出 52 个参与胚胎发生的基因,其中 22 个参与核酸代谢。我们的结果表明,AtBUD13 通过影响前体 mRNA 剪接在早期胚胎发育中发挥关键作用。