Yu Huihui, Du Qian, Campbell Malachy, Yu Bin, Walia Harkamal, Zhang Chi
School of Biological Sciences, University of Nebraska, Lincoln, NE, 68588, USA.
Department of Agronomy and Horticulture, University of Nebraska, Lincoln, NE, 68583, USA.
New Phytol. 2021 May;230(3):1273-1287. doi: 10.1111/nph.17189. Epub 2021 Feb 14.
Pre-mRNA splicing is an essential step for the regulation of gene expression. In order to specifically capture splicing variants in plants for genome-wide association studies (GWAS), we developed a software tool to quantify and visualise Variations of Splicing in Population (VaSP). VaSP can quantify splicing variants from short-read RNA-seq datasets and discover genotype-specific splicing (GSS) events, which can be used to prioritise causal pre-mRNA splicing events in GWAS. We applied our method to an RNA-seq dataset with 328 samples from 82 genotypes from a rice diversity panel exposed to optimal and saline growing conditions. In total, 764 significant GSS events were identified in salt stress conditions. GSS events were used as markers for a GWAS with the shoot Na accumulation, which identified six GSS events in five genes significantly associated with the shoot Na content. Two of these genes, OsNUC1 and OsRAD23 emerged as top candidate genes with splice variants that exhibited significant divergence between the variants for shoot growth under salt stress conditions. VaSP is a versatile tool for alternative splicing analysis in plants and a powerful tool for prioritising candidate causal pre-mRNA splicing and corresponding genomic variations in GWAS.
前体信使核糖核酸(pre-mRNA)剪接是基因表达调控的关键步骤。为了在全基因组关联研究(GWAS)中特异性捕获植物中的剪接变体,我们开发了一种软件工具,用于量化和可视化群体剪接变异(VaSP)。VaSP可以从短读长RNA测序数据集中量化剪接变体,并发现基因型特异性剪接(GSS)事件,这些事件可用于在GWAS中对因果前体信使核糖核酸剪接事件进行优先级排序。我们将我们的方法应用于一个RNA测序数据集,该数据集包含来自水稻多样性群体的82个基因型的328个样本,这些样本分别处于最佳生长条件和盐胁迫生长条件下。在盐胁迫条件下,总共鉴定出764个显著的GSS事件。GSS事件被用作全基因组关联研究的标记,以研究地上部钠积累情况,结果在五个基因中鉴定出六个与地上部钠含量显著相关的GSS事件。其中两个基因,OsNUC1和OsRAD23成为顶级候选基因,其剪接变体在盐胁迫条件下地上部生长的变体之间表现出显著差异。VaSP是一种用于植物可变剪接分析的通用工具,也是一种在GWAS中对候选因果前体信使核糖核酸剪接和相应基因组变异进行优先级排序的强大工具。