Shi Xueping, Zhang Cuijie, Liu Qinhong, Zhang Zhe, Zheng Bo, Bao Manzhu
Key Laboratory of Horticultural Plant Biology of Ministry of Education, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, P. R. China.
BMC Genomics. 2016 Jan 5;17:26. doi: 10.1186/s12864-015-2357-8.
Somatic embryogenesis is a notable illustration of cell totipotency, by which somatic cells undergo dedifferentiation and then differentiate into somatic embryos. Our previous work demonstrated that pretreatment of immature zygotic embryos with 0.5 M sucrose solution for 72 h efficiently induced somatic embryo initiation in camphor tree. To better understand the molecular basis of somatic embryogenesis induced by osmotic stress, de novo transcriptome sequencing of three tissues of camphor tree (immature zygotic embryos, sucrose-pretreated immature zygotic embryos, and somatic embryos induced from sucrose-pretreated zygotic embryos) were conducted using Illumina Hiseq 2000 platform.
A total of 30.70 G high quality clean reads were obtained from cDNA libraries of the three samples. The overall de novo assembly of cDNA sequence data generated 205592 transcripts, with an average length of 998 bp. 114229 unigenes (55.56 % of all transcripts) with an average length of 680 bp were annotated with gene descriptions, gene ontology terms or metabolic pathways based on Blastx search against Nr, Nt, Swissprot, GO, COG/KOG, and KEGG databases. CEGMA software identified 237 out of 248 ultra-conserved core proteins as 'complete' in the transcriptome assembly, showing a completeness of 95.6 %. A total of 897 genes previously annotated to be potentially involved in somatic embryogenesis were identified. Comparative transcriptome analysis showed that a total of 3335 genes were differentially expressed in the three samples. The differentially expressed genes were divided into six groups based on K-means clustering. Expression level analysis of 52 somatic embryogenesis-related genes indicated a high correlation between RNA-seq and qRT-PCR data. Gene enrichment analysis showed significantly differential expression of genes responding to stress and stimulus.
The present work reported a de novo transcriptome assembly and global analysis focused on gene expression changes during initiation and formation of somatic embryos in camphor tree. Differential expression of somatic embryogenesis-related genes indicates that sucrose induced somatic embryogenesis may share or partly share the mechanisms of somatic embryogenesis induced by plant hormones. This study provides comprehensive transcript information and gene expression data for camphor tree. It could also serve as an important platform resource for further functional studies in plant embryogenesis.
体细胞胚胎发生是细胞全能性的一个显著例证,通过该过程体细胞经历去分化,然后分化形成体细胞胚。我们之前的研究表明,用0.5M蔗糖溶液预处理未成熟合子胚72小时可有效诱导樟树体细胞胚的起始。为了更好地理解渗透胁迫诱导体细胞胚胎发生的分子基础,使用Illumina Hiseq 2000平台对樟树的三种组织(未成熟合子胚、蔗糖预处理的未成熟合子胚以及由蔗糖预处理的合子胚诱导产生的体细胞胚)进行了从头转录组测序。
从三个样品的cDNA文库中总共获得了30.70G高质量的clean reads。cDNA序列数据的总体从头组装产生了205592个转录本,平均长度为998bp。基于对Nr、Nt、Swissprot、GO、COG/KOG和KEGG数据库的Blastx搜索,114229个单基因(占所有转录本的55.56%)被注释了基因描述、基因本体术语或代谢途径,平均长度为680bp。CEGMA软件在转录组组装中鉴定出248个超保守核心蛋白中的237个为“完整”,完整性为95.6%。总共鉴定出897个先前注释为可能参与体细胞胚胎发生的基因。比较转录组分析表明,三个样品中共有3335个基因差异表达。基于K均值聚类,差异表达基因被分为六组。对52个与体细胞胚胎发生相关基因的表达水平分析表明,RNA-seq和qRT-PCR数据之间具有高度相关性。基因富集分析显示,响应胁迫和刺激的基因存在显著差异表达。
本研究报道了樟树体细胞胚起始和形成过程中基因表达变化的从头转录组组装和全局分析。体细胞胚胎发生相关基因的差异表达表明,蔗糖诱导的体细胞胚胎发生可能与植物激素诱导的体细胞胚胎发生共享或部分共享机制。本研究为樟树提供了全面的转录信息和基因表达数据。它也可以作为植物胚胎发生进一步功能研究的重要平台资源。