Hu Jinglei, Liu Mingxia, Wang Dongxia, Liang Yunlong, Zong Yuan, Li Yun, Cao Dong, Liu Baolong
Key Laboratory of Crop Molecular Breeding, Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, Qinghai, China.
College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.
Front Plant Sci. 2024 Oct 1;15:1439547. doi: 10.3389/fpls.2024.1439547. eCollection 2024.
Ethyl methanesulfonate (EMS)-induced mutagenesis is a prominent method for generating plant mutants, often resulting in chimera plants; however, their transcriptional and genetic characteristic remain elusive. In this investigation, chimera pea ( L.) specimens, labeled GY1 and GY2, exhibiting a distinctive phenotype with yellow and green leaves were meticulously cultivated via sequential double EMS mutagenesis. The observed color disparity between the yellow and green leaves was attributed to a significant reduction in chlorophyll content coupled with heightened lutein levels in both chimeric variants. Transcriptome profiling revealed the enrichment of differentially expressed genes in both GY1 and GY2, specifically implicating Kyoto Encyclopedia of Genes and Genomes pathways linked to amino acid biosynthesis and ribosome development, alongside Gene Ontology (GO) biological processes linked with stress response mechanisms. Few structural genes associated with chlorophyll and lutein biosynthesis exhibited discernible differential expression. Despite these functional similarities, distinctive nuances were evident between specimens, with GY1 exhibiting enrichment in GO pathways related to chloroplast development and GY2 showing enrichment for ribosome development pathways. Single-nucleotide polymorphism (SNP) analysis uncovered a shared pool of 599 and 598 polymorphisms in the yellow and green leaves of GY1 and GY2, respectively, likely stemming from the initial EMS mutagenesis step. Further investigation revealed an increased number of unique SNPs in the yellow leaves following the second EMS application, whereas the green leaves exhibited sparse and unique SNP occurrences, suggestive of potential evasion from secondary mutagenesis. This inherent genetic variability underpins the mechanism underlying the formation of chimera plants. Predominant base mutations induced by EMS were characterized by G/A and C/T transitions, constituting 74.1% of the total mutations, aligning with established EMS mutation induction paradigms. Notably, genes encoding the eukaryotic translation initiation factor eIIso4G and the ubiquitin ligase RKP, known to modulate leaf color in model plants, harbored two SNPs in the yellow leaves of both GY1 and GY2, implicating their putative role in the yellow leaf phenotype. Collectively, this study provides novel insights into the transcriptional and genetic characteristics of chimera plants via EMS-induced mutagenesis.
甲磺酸乙酯(EMS)诱导的诱变是产生植物突变体的一种重要方法,常常会产生嵌合体植物;然而,它们的转录和遗传特征仍不清楚。在本研究中,通过连续两次EMS诱变精心培育了标记为GY1和GY2的嵌合体豌豆(L.)标本,其呈现出黄叶和绿叶的独特表型。观察到的黄叶和绿叶之间的颜色差异归因于两种嵌合体变体中叶绿素含量的显著降低以及叶黄素水平的升高。转录组分析揭示了GY1和GY2中差异表达基因的富集,具体涉及与氨基酸生物合成和核糖体发育相关的京都基因与基因组百科全书途径,以及与应激反应机制相关的基因本体(GO)生物学过程。很少有与叶绿素和叶黄素生物合成相关的结构基因表现出明显的差异表达。尽管有这些功能上的相似性,但标本之间仍存在明显的细微差别,GY1在与叶绿体发育相关的GO途径中表现出富集,而GY2在核糖体发育途径中表现出富集。单核苷酸多态性(SNP)分析发现,GY1和GY2的黄叶和绿叶中分别有599个和598个多态性位点的共享库,这可能源于最初的EMS诱变步骤。进一步研究发现,第二次EMS处理后黄叶中独特SNP的数量增加,而绿叶中独特SNP的出现稀疏且独特,这表明可能逃避了二次诱变。这种内在的遗传变异性是嵌合体植物形成机制的基础。EMS诱导的主要碱基突变以G/A和C/T转换为特征,占总突变的74.1%,与已确立的EMS诱变诱导模式一致。值得注意的是,已知在模式植物中调节叶片颜色的编码真核翻译起始因子eIIso4G和泛素连接酶RKP的基因,在GY1和GY2的黄叶中都有两个SNP,这暗示了它们在黄叶表型中的假定作用。总的来说,本研究通过EMS诱导的诱变对嵌合体植物的转录和遗传特征提供了新的见解。