Dutta Haragopal, Mishra Gyan P, Aski Muraleedhar S, Bosamia Tejas C, Mishra Dwijesh C, Bhati Jyotika, Sinha Subodh Kumar, Vijay Dunna, C T Manjunath Prasad, Das Shouvik, Pawar Prashant Anupama-Mohan, Kumar Atul, Tripathi Kuldeep, Kumar Ranjeet Ranjan, Yadava Devendra Kumar, Kumar Shiv, Dikshit Harsh Kumar
Division of Genetics, Indian Agricultural Research Institute, New Delhi, India.
Plant Omics Division, Central Salt and Marine Chemicals Research Institute, Bhavnagar, India.
Front Genet. 2022 Aug 10;13:942079. doi: 10.3389/fgene.2022.942079. eCollection 2022.
Market class, cooking time, quality, and milled grain yield are largely influenced by the seed size and shape of the lentil ( Medik.); thus, they are considered to be important quality traits. To unfold the pathways regulating seed size in lentils, a transcriptomic approach was performed using large-seeded (L4602) and small-seeded (L830) genotypes. The study has generated nearly 375 million high-quality reads, of which 98.70% were properly aligned to the reference genome. Among biological replicates, very high similarity in fragments per kilobase of exon per million mapped fragments values (R > 0.9) showed the consistency of RNA-seq results. Various differentially expressed genes associated mainly with the hormone signaling and cell division pathways, transcription factors, kinases, etc. were identified as having a role in cell expansion and seed growth. A total of 106,996 unigenes were used for differential expression (DE) analysis. String analysis identified various modules having certain key proteins like Ser/Thr protein kinase, seed storage protein, DNA-binding protein, microtubule-associated protein, etc. In addition, some growth and cell division-related micro-RNAs like miR3457 (cell wall formation), miR1440 (cell proliferation and cell cycles), and miR1533 (biosynthesis of plant hormones) were identified as having a role in seed size determination. Using RNA-seq data, 5254 EST-SSR primers were generated as a source for future studies aiming for the identification of linked markers. validation using Genevestigator was done for the Ser/Thr protein kinase, ethylene response factor, and Myb transcription factor genes. It is of interest that the xyloglucan endotransglucosylase gene was found differentially regulated, suggesting their role during seed development; however, at maturity, no significant differences were recorded for various cell wall parameters including cellulose, lignin, and xylose content. This is the first report on lentils that has unfolded the key seed size regulating pathways and unveiled a theoretical way for the development of lentil genotypes having customized seed sizes.
市场等级、烹饪时间、品质和碾磨谷物产量在很大程度上受小扁豆(Medik.)种子大小和形状的影响;因此,它们被认为是重要的品质性状。为了揭示调控小扁豆种子大小的途径,使用大粒(L4602)和小粒(L830)基因型进行了转录组学研究。该研究产生了近3.75亿条高质量 reads,其中98.70% 与参考基因组正确比对。在生物学重复中,每百万映射片段中外显子每千碱基片段值的极高相似性(R > 0.9)表明RNA-seq结果的一致性。鉴定出各种主要与激素信号传导和细胞分裂途径、转录因子、激酶等相关的差异表达基因在细胞扩张和种子生长中起作用。总共106,996个单基因用于差异表达(DE)分析。STRING分析确定了具有某些关键蛋白的各种模块,如丝氨酸/苏氨酸蛋白激酶、种子贮藏蛋白、DNA结合蛋白、微管相关蛋白等。此外,一些与生长和细胞分裂相关的微小RNA,如miR3457(细胞壁形成)、miR1440(细胞增殖和细胞周期)和miR1533(植物激素生物合成)被确定在种子大小决定中起作用。利用RNA-seq数据,生成了5254个EST-SSR引物,作为未来旨在鉴定连锁标记研究的来源。对丝氨酸/苏氨酸蛋白激酶、乙烯反应因子和Myb转录因子基因进行了使用Genevestigator的验证。有趣的是,发现木葡聚糖内转糖基酶基因受到差异调控,表明它们在种子发育过程中的作用;然而,在成熟时,包括纤维素、木质素和木糖含量在内的各种细胞壁参数没有记录到显著差异。这是关于小扁豆的第一份报告,揭示了关键的种子大小调控途径,并为开发具有定制种子大小的小扁豆基因型开辟了一条理论途径。