Singla Bhumica, Tyagi Akhilesh K, Khurana Jitendra P, Khurana Paramjit
Interdisciplinary Centre for Plant Genomics, Department of Plant Molecular Biology, University of Delhi South Campus, Benito Juarez Road, New Delhi 110021, India.
Plant Mol Biol. 2007 Nov;65(5):677-92. doi: 10.1007/s11103-007-9234-z. Epub 2007 Sep 12.
Somatic embryogenesis is a notable illustration of plant totipotency and involves reprogramming of development in somatic cells toward the embryogenic pathway. Auxins are key components as their exogenous application recuperates the embryogenic potential of the mitotically quiescent somatic cells. In order to unravel the molecular basis of somatic embryogenesis, cDNA library was made from the regeneration proficient wheat leaf base segments treated with auxin. In total, 1440 clones were sequenced and among these 1,196 good quality sequences were assembled into 270 contigs and 425 were singletons. By reverse northern analysis, a total of 57 clones were found to be upregulated during somatic embryogenesis, 64 during 2,4-D treatment, and 170 were common to 2,4-D treatment and somatic embryogenesis. A substantial number of genes involved in hormone response, signal transduction cascades, defense, anti-oxidation, programmed cell death/senescence and cell division were identified and characterized partially. Analysis of data of select genes suggests that the induction phase of somatic embryogenesis is accompanied by the expression of genes that may also be involved in zygotic embryogenesis. The developmental reprogramming process may in fact involve multiple cellular pathways and unfolding of as yet unknown molecular events. Thus, an interaction network draft using bioinformatics and system biology strategy was constructed. The outcome of a systematic and comprehensive analysis of somatic embryogenesis associated interactome in a monocot leaf base system is presented.
体细胞胚胎发生是植物全能性的一个显著例证,涉及体细胞发育重编程至胚胎发生途径。生长素是关键成分,因为其外源应用可恢复有丝分裂静止体细胞的胚胎发生潜能。为了揭示体细胞胚胎发生的分子基础,从用生长素处理的具有再生能力的小麦叶基部片段构建了cDNA文库。总共对1440个克隆进行了测序,其中1196个高质量序列被组装成270个重叠群,425个为单拷贝序列。通过反向Northern分析,共发现57个克隆在体细胞胚胎发生过程中上调,64个在2,4 - D处理过程中上调,170个在2,4 - D处理和体细胞胚胎发生过程中均上调。鉴定并部分表征了大量参与激素反应、信号转导级联、防御、抗氧化、程序性细胞死亡/衰老和细胞分裂的基因。对选定基因数据的分析表明,体细胞胚胎发生的诱导阶段伴随着可能也参与合子胚胎发生的基因的表达。发育重编程过程实际上可能涉及多个细胞途径和尚未知晓的分子事件的展开。因此,利用生物信息学和系统生物学策略构建了一个相互作用网络草图。本文展示了对单子叶基部系统中与体细胞胚胎发生相关的相互作用组进行系统全面分析的结果。