Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Inhoffenstr. 7b, 38124 Braunschweig, Germany.
Plant Cell Rep. 2012 Jun;31(6):1061-71. doi: 10.1007/s00299-011-1225-5. Epub 2012 Jan 18.
Although many genes are supposed to be a part of plant cell tolerance mechanisms against osmotic or salt stress, their influence on tolerance towards stress during cryopreservation procedures has rarely been investigated. For instance, the overexpression of the pathogenesis-related gene 10a (pr-10a) leads to improved osmotic tolerance in a transgenic cell culture of Solanum tuberosum cv. Désirée. In this study, a cryopreservation method, consisting of osmotic pretreatment, cryoprotection with DMSO and controlled-rate freezing, was used to characterize the relation between cryopreservation success and pr-10a expression in suspension cultures of S. tuberosum wild-type cells and cells overexpressing pathogenesis-related protein 10a (Pr-10a). By varying the sorbitol concentration, thus modifying the strength of the osmotic stress during the pretreatment phase, it can be shown that the wild type can successfully be cryopreserved only in a relatively narrow range of sorbitol concentrations, while the pr-10a overexpression leads to an enhanced cryopreservation success over the whole range of applied sorbitol concentrations. Together with transcription data we show that the pr-10a overexpression causes an enhanced osmotic tolerance, which in turn leads to enhanced cryopreservability, but also indicates a role of pr-10a in signal transduction. An increased cryopreservability of the transgenic cell line occurs for pretreatments longer than 24 h. Since both genotypes, characterized by distinct baseline levels of expression, exhibited similar patterns of expression induction, the induction of pr-10a appears to be a key step in the stress signal transduction of plant cells under osmotic stress.
尽管许多基因被认为是植物细胞耐受渗透或盐胁迫机制的一部分,但它们对冷冻保存过程中耐受胁迫的影响很少被研究。例如,过表达病程相关蛋白 10a (pr-10a)可导致马铃薯 cv. Désirée 的转基因细胞培养物的耐渗性提高。在这项研究中,采用包括渗透预处理、二甲亚砜保护和控制速率冷冻的冷冻保存方法,来研究悬浮培养的马铃薯野生型细胞和过表达病程相关蛋白 10a (Pr-10a)的细胞中冷冻保存成功与 pr-10a 表达之间的关系。通过改变山梨醇浓度,从而改变预处理阶段的渗透胁迫强度,可以表明野生型只能在相对较窄的山梨醇浓度范围内成功冷冻保存,而过表达 pr-10a 则导致在整个应用山梨醇浓度范围内提高了冷冻保存成功率。结合转录数据,我们表明过表达 pr-10a 导致增强的耐渗性,这反过来又导致增强的冷冻保存能力,但也表明 pr-10a 在信号转导中的作用。对于预处理时间超过 24 小时的转化细胞系,冷冻保存能力增强。由于这两种基因型具有不同的基础表达水平,表现出相似的表达诱导模式,因此 pr-10a 的诱导似乎是植物细胞在渗透胁迫下应激信号转导的关键步骤。