Skorupa Monika, Gołębiewski Marcin, Domagalski Krzysztof, Kurnik Katarzyna, Abu Nahia Karim, Złoch Michał, Tretyn Andrzej, Tyburski Jarosław
Chair of Plant Physiology and Biotechnology, Nicolaus Copernicus University, Lwowska 1, 87-100 Toruń, Poland.
Chair of Plant Physiology and Biotechnology, Nicolaus Copernicus University, Lwowska 1, 87-100 Toruń, Poland; Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus University, Wileńska 4, 87-100 Toruń, Poland.
Plant Sci. 2016 Feb;243:56-70. doi: 10.1016/j.plantsci.2015.11.007. Epub 2015 Nov 26.
Beta vulgaris ssp. maritima is a halophytic relative of cultivated beets. In the present work a transcriptome response to acute salt stress imposed to excised leaves of sea beet was investigated. Salt treatments consisted of adding NaCl directly to the transpiration stream by immersing the petioles of excised leaves into the salt solutions. Sequencing libraries were generated from leaves subjected to either moderate or strong salt stress. Control libraries were constructed from untreated leaves. Sequencing was performed using the Illumina MiSeq platform. We obtained 32970 unigenes by assembling the pooled reads from all the libraries with Trinity software. Screening the nr database returned 18,362 sequences with functional annotation. Using the reference transcriptome we identified 1,246 genes that were differentially expressed after 48 h of NaCl stress. Genes related to several cellular functions such as membrane transport, osmoprotection, molecular chaperoning, redox metabolism or protein synthesis were differentially expressed in response to salt stress. The response of sea beet leaves to salt treatments was marked out by transcriptomic up-regulation of genes related to photosynthetic carbon fixation, ribosome biogenesis, cell wall-building and cell wall expansion. Furthermore, several novel and undescribed transcripts were responsive to salinity in leaves of sea beet.
海甜菜(Beta vulgaris ssp. maritima)是栽培甜菜的一种盐生近缘种。在本研究中,我们调查了海甜菜离体叶片对急性盐胁迫的转录组反应。盐处理是通过将离体叶片的叶柄浸入盐溶液中,直接向蒸腾流中添加氯化钠。从经受中度或重度盐胁迫的叶片中构建测序文库。从未处理的叶片构建对照文库。使用Illumina MiSeq平台进行测序。我们用Trinity软件组装来自所有文库的混合 reads,得到了32970个单基因。筛选nr数据库返回了18362个具有功能注释的序列。使用参考转录组,我们鉴定出1246个在NaCl胁迫48小时后差异表达的基因。与膜运输、渗透保护、分子伴侣、氧化还原代谢或蛋白质合成等几种细胞功能相关的基因在盐胁迫下差异表达。海甜菜叶片对盐处理的反应表现为与光合碳固定、核糖体生物发生、细胞壁构建和细胞壁扩展相关的基因的转录组上调。此外,一些新的和未描述的转录本对海甜菜叶片中的盐度有反应。