Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Nanjing, 210037, China.
Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518063, China.
Plant J. 2020 Jul;103(1):357-378. doi: 10.1111/tpj.14735. Epub 2020 Apr 24.
Intron-containing genes have the ability to generate multiple transcript isoforms by splicing, thereby greatly expanding the eukaryotic transcriptome and proteome. In eukaryotic cells, precursor mRNA (pre-mRNA) splicing is performed by a mega-macromolecular complex defined as a spliceosome. Among its splicing components, U1 small nuclear ribonucleoprotein (U1 snRNP) is the smallest subcomplex involved in early spliceosome assembly and 5'-splice site recognition. Its central component, named U1-70K, has been extensively characterized in animals and yeast. Very few investigations on U1-70K genes have been conducted in plants, however. To this end, we performed a comprehensive study to systematically identify 115 U1-70K genes from 67 plant species, ranging from algae to angiosperms. Phylogenetic analysis suggested that the expansion of the plant U1-70K gene family was likely to have been driven by whole-genome duplications. Subsequent comparisons of gene structures, protein domains, promoter regions and conserved splicing patterns indicated that plant U1-70Ks are likely to preserve their conserved molecular function across plant lineages and play an important functional role in response to environmental stresses. Furthermore, genetic analysis using T-DNA insertion mutants suggested that Arabidopsis U1-70K may be involved in response to osmotic stress. Our results provide a general overview of this gene family in Viridiplantae and will act as a reference source for future mechanistic studies on this U1 snRNP-specific splicing factor.
内含子基因通过剪接具有产生多个转录体同工型的能力,从而极大地扩展了真核生物的转录组和蛋白质组。在真核细胞中,前体 mRNA(pre-mRNA)剪接是由一个定义为剪接体的巨型大分子复合物完成的。在其剪接成分中,U1 小核核糖核蛋白(U1 snRNP)是参与早期剪接体组装和 5'剪接位点识别的最小亚复合物。其核心成分,命名为 U1-70K,在动物和酵母中得到了广泛的研究。然而,在植物中对 U1-70K 基因的研究非常少。为此,我们进行了一项全面的研究,从 67 种植物物种中系统地鉴定了 115 个 U1-70K 基因,范围从藻类到被子植物。系统发育分析表明,植物 U1-70K 基因家族的扩张可能是由全基因组加倍驱动的。随后对基因结构、蛋白质结构域、启动子区域和保守剪接模式的比较表明,植物 U1-70Ks 可能在植物谱系中保留了其保守的分子功能,并在应对环境胁迫中发挥重要的功能作用。此外,使用 T-DNA 插入突变体的遗传分析表明,拟南芥 U1-70K 可能参与了对渗透胁迫的响应。我们的研究结果为维管植物中的这个基因家族提供了一个总体概述,并将为未来对这个 U1 snRNP 特异性剪接因子的机制研究提供参考。