Jyothi-Prakash Pavithra A, Mohanty Bijayalaxmi, Wijaya Edward, Lim Tit-Meng, Lin Qingsong, Loh Chiang-Shiong, Kumar Prakash P
BMC Plant Biol. 2014 Nov 18;14:291. doi: 10.1186/s12870-014-0291-6.
Salt stress is a major challenge for growth and development of plants. The mangrove tree Avicennia officinalis has evolved salt tolerance mechanisms such as salt secretion through specialized glands on its leaves. Although a number of structural studies on salt glands have been done, the molecular mechanism of salt secretion is not clearly understood. Also, studies to identify salt gland-specific genes in mangroves have been scarce.
By subtractive hybridization (SH) of cDNA from salt gland-rich cell layers (tester) with mesophyll tissues as the driver, several Expressed Sequence Tags (ESTs) were identified. The major classes of ESTs identified include those known to be involved in regulating metabolic processes (37%), stress response (17%), transcription (17%), signal transduction (17%) and transport functions (12%). A visual interactive map generated based on predicted functional gene interactions of the identified ESTs suggested altered activities of hydrolase, transmembrane transport and kinases. Quantitative Real-Time PCR (qRT-PCR) was carried out to validate the expression specificity of the ESTs identified by SH. A Dehydrin gene was chosen for further experimental analysis, because it is significantly highly expressed in salt gland cells, and dehydrins are known to be involved in stress remediation in other plants. Full-length Avicennia officinalis Dehydrin1 (AoDHN1) cDNA was obtained by Rapid Amplification of cDNA Ends. Phylogenetic analysis and further characterization of this gene suggested that AoDHN1 belongs to group II Late Embryogenesis Abundant proteins. qRT-PCR analysis of Avicennia showed up-regulation of AoDHN1 in response to salt and drought treatments. Furthermore, some functional insights were obtained by growing E. coli cells expressing AoDHN1. Growth of E. coli cells expressing AoDHN1 was significantly higher than that of the control cells without AoDHN1 under salinity and drought stresses, suggesting that the mangrove dehydrin protein helps to mitigate the abiotic stresses.
Thirty-four ESTs were identified to be enriched in salt gland-rich tissues of A. officinalis leaves. qRT-PCR analysis showed that 10 of these were specifically enriched in the salt gland-rich tissues. Our data suggest that one of the selected genes, namely, AoDHN1 plays an important role to mitigate salt and drought stress responses.
盐胁迫是植物生长发育面临的主要挑战。红树植物海榄雌进化出了耐盐机制,如通过叶片上的特化腺体分泌盐分。尽管已经对盐腺进行了多项结构研究,但盐分分泌的分子机制仍不清楚。此外,在红树林中鉴定盐腺特异性基因的研究也很少。
通过以叶肉组织为驱动,对富含盐腺的细胞层(测试样本)的cDNA进行消减杂交(SH),鉴定出了几个表达序列标签(EST)。鉴定出的主要EST类别包括已知参与调节代谢过程(37%)、应激反应(17%)、转录(17%)、信号转导(17%)和运输功能(12%)的那些。基于所鉴定EST的预测功能基因相互作用生成的可视化交互图谱表明水解酶、跨膜运输和激酶的活性发生了改变。进行了定量实时PCR(qRT-PCR)以验证通过SH鉴定的EST的表达特异性。选择了一个脱水素基因进行进一步的实验分析,因为它在盐腺细胞中显著高表达,并且已知脱水素在其他植物中参与应激修复。通过cDNA末端快速扩增获得了全长海榄雌脱水素1(AoDHN1)cDNA。该基因的系统发育分析和进一步表征表明AoDHN1属于II组晚期胚胎丰富蛋白。对海榄雌的qRT-PCR分析表明,AoDHN1在盐和干旱处理下上调。此外,通过培养表达AoDHN1的大肠杆菌细胞获得了一些功能见解。在盐度和干旱胁迫下,表达AoDHN1的大肠杆菌细胞的生长明显高于不表达AoDHN1的对照细胞,这表明红树林脱水素蛋白有助于减轻非生物胁迫。
在海榄雌叶片富含盐腺的组织中鉴定出34个EST富集。qRT-PCR分析表明其中10个在富含盐腺的组织中特异性富集。我们的数据表明,所选基因之一,即AoDHN1在减轻盐和干旱胁迫反应中起重要作用。