Huang Tsai-Lien, Huang Li-Yao, Fu Shih-Feng, Trinh Ngoc-Nam, Huang Hao-Jen
Department of Life Sciences, National Cheng Kung University, No. 1 University Road, Tainan City, 701, Taiwan.
Plant Mol Biol. 2014 Sep;86(1-2):157-70. doi: 10.1007/s11103-014-0219-4. Epub 2014 Jul 24.
Cr(VI) is the most toxic valency form of Cr, but its toxicity targets and the cellular systems contributing to acquisition of tolerance remain to be resolved at the molecular level in plants. We used microarray assay to analyze the transcriptomic profiles of rice roots in response to Cr(VI) stress. Gene ontology analysis revealed that the 2,688 Cr-responsive genes were involved in binding activity, metabolic process, biological regulation, cellular process and catalytic activity. More transcripts were responsive to Cr(VI) during long-term exposure (24 h, 2,097 genes), than short-term exposure (1- and 3-h results pooled, 1,181 genes). Long-term Cr(VI)-regulated genes are involved in cytokinin signaling, the ubiquitin-proteasome system pathway, DNA repair and Cu transportation. The expression of AS2 transcription factors was specifically modulated by long-term Cr(VI) stress. The protein kinases receptor-like cytoplasmic kinase and receptor-like kinase in flowers 3 were significantly upregulated with only short-term Cr(VI) exposure. In addition, 4 mitogen-activated protein kinase kinase kinases, 1 mitogen-activated protein kinase (MAPK) and 1 calcium-dependent protein kinase (CDPK) were upregulated with short-term Cr(VI) treatment. Expression of reactive oxygen species and calcium and activity of MAPKs and CDPK-like kinases were induced with increasing Cr(VI) concentration. These results may provide new insights into understanding the mechanisms of Cr toxicity and tolerance during different stages in rice roots.
六价铬是铬毒性最强的价态形式,但其毒性靶点以及植物中有助于获得耐受性的细胞系统在分子水平上仍有待解决。我们使用微阵列分析来研究水稻根系在六价铬胁迫下的转录组谱。基因本体分析表明,2688个对六价铬有响应的基因参与了结合活性、代谢过程、生物调控、细胞过程和催化活性。与短期暴露(将1小时和3小时的结果合并,共1181个基因)相比,长期暴露(24小时,2097个基因)期间有更多的转录本对六价铬有响应。长期受六价铬调控的基因参与细胞分裂素信号传导、泛素 - 蛋白酶体系统途径、DNA修复和铜转运。AS2转录因子的表达受到长期六价铬胁迫的特异性调节。仅在短期六价铬暴露下,类受体细胞质激酶和花3中的类受体激酶这两种蛋白激酶显著上调。此外,在短期六价铬处理下,4种丝裂原活化蛋白激酶激酶激酶、1种丝裂原活化蛋白激酶(MAPK)和1种钙依赖性蛋白激酶(CDPK)上调。随着六价铬浓度的增加,活性氧、钙的表达以及MAPK和类CDPK激酶的活性被诱导。这些结果可能为理解水稻根系不同阶段六价铬毒性和耐受性的机制提供新的见解。