Rajesh M K, Fayas T P, Naganeeswaran S, Rachana K E, Bhavyashree U, Sajini K K, Karun Anitha
Division of Crop Improvement, ICAR-Central Plantation Crops Research Institute, Kasaragod, 671124, Kerala, India.
Protoplasma. 2016 May;253(3):913-928. doi: 10.1007/s00709-015-0856-8. Epub 2015 Jul 26.
Production and supply of quality planting material is significant to coconut cultivation but is one of the major constraints in coconut productivity. Rapid multiplication of coconut through in vitro techniques, therefore, is of paramount importance. Although somatic embryogenesis in coconut is a promising technique that will allow for the mass production of high quality palms, coconut is highly recalcitrant to in vitro culture. In order to overcome the bottlenecks in coconut somatic embryogenesis and to develop a repeatable protocol, it is imperative to understand, identify, and characterize molecular events involved in coconut somatic embryogenesis pathway. Transcriptome analysis (RNA-Seq) of coconut embryogenic calli, derived from plumular explants of West Coast Tall cultivar, was undertaken on an Illumina HiSeq 2000 platform. After de novo transcriptome assembly and functional annotation, we have obtained 40,367 transcripts which showed significant BLASTx matches with similarity greater than 40 % and E value of ≤10(-5). Fourteen genes known to be involved in somatic embryogenesis were identified. Quantitative real-time PCR (qRT-PCR) analyses of these 14 genes were carried in six developmental stages. The result showed that CLV was upregulated in the initial stage of callogenesis. Transcripts GLP, GST, PKL, WUS, and WRKY were expressed more in somatic embryo stage. The expression of SERK, MAPK, AP2, SAUR, ECP, AGP, LEA, and ANT were higher in the embryogenic callus stage compared to initial culture and somatic embryo stages. This study provides the first insights into the gene expression patterns during somatic embryogenesis in coconut.
优质种植材料的生产和供应对椰子种植至关重要,但却是影响椰子产量的主要制约因素之一。因此,通过体外技术快速繁殖椰子至关重要。尽管椰子体细胞胚胎发生是一种很有前景的技术,能够实现高质量棕榈树的大规模生产,但椰子对体外培养具有高度的顽拗性。为了克服椰子体细胞胚胎发生中的瓶颈并开发可重复的方案,了解、鉴定和表征参与椰子体细胞胚胎发生途径的分子事件势在必行。我们在Illumina HiSeq 2000平台上对源自西海岸高种椰子品种胚轴外植体的胚性愈伤组织进行了转录组分析(RNA测序)。经过从头转录组组装和功能注释,我们获得了40367个转录本,这些转录本显示出显著的BLASTx匹配,相似度大于40%,E值≤10-5。鉴定出14个已知参与体细胞胚胎发生的基因。对这14个基因在六个发育阶段进行了定量实时PCR(qRT-PCR)分析。结果表明,CLV在愈伤组织形成初期上调。转录本GLP、GST、PKL、WUS和WRKY在体细胞胚胎阶段表达更多。与初始培养阶段和体细胞胚胎阶段相比,SERK、MAPK、AP2、SAUR、ECP、AGP、LEA和ANT在胚性愈伤组织阶段的表达更高。本研究首次深入了解了椰子体细胞胚胎发生过程中的基因表达模式。