Wu Tao, Yang Chunyan, Ding Baoxu, Feng Zhiming, Wang Qian, He Jun, Tong Jianhua, Xiao Langtao, Jiang Ling, Wan Jianmin
State Key Laboratory of Crop Genetics and Germplasm Enhancement, Research Center of Jiangsu Plant Gene Engineering, Nanjing Agricultural University, Nanjing, 210095, China.
Hunan Provincial Key Laboratory of Phytohormones and Growth Development, Hunan Agricultural University, Changsha, 410128, China.
Plant Physiol Biochem. 2016 Feb;99:27-38. doi: 10.1016/j.plaphy.2015.12.001. Epub 2015 Dec 9.
Seed dormancy in rice is an important trait related to the pre-harvest sprouting resistance. In order to understand the molecular mechanisms of seed dormancy, gene expression was investigated by transcriptome analysis using seeds of the strongly dormant cultivar N22 and its less dormant mutants Q4359 and Q4646 at 24 days after heading (DAH). Microarray data revealed more differentially expressed genes in Q4359 than in Q4646 compared to N22. Most genes differing between Q4646 and N22 also differed between Q4359 and N22. GO analysis of genes differentially expressed in both Q4359 and Q4646 revealed that some genes such as those for starch biosynthesis were repressed, whereas metabolic genes such as those for carbohydrate metabolism were enhanced in Q4359 and Q4646 seeds relative to N22. Expression of some genes involved in cell redox homeostasis and chromatin remodeling differed significantly only between Q4359 and N22. The results suggested a close correlation between cell redox homeostasis, chromatin remodeling and seed dormancy. In addition, some genes involved in ABA signaling were down-regulated, and several genes involved in GA biosynthesis and signaling were up-regulated. These observations suggest that reduced seed dormancy in Q4359 was regulated by ABA-GA antagonism. A few differentially expressed genes were located in the regions containing qSdn-1 and qSdn-5 suggesting that they could be candidate genes underlying seed dormancy. Our work provides useful leads to further determine the underling mechanisms of seed dormancy and for cloning seed dormancy genes from N22.
水稻种子休眠是与抗穗发芽相关的重要性状。为了解种子休眠的分子机制,利用强休眠品种N22及其弱休眠突变体Q4359和Q4646抽穗后24天(DAH)的种子,通过转录组分析研究基因表达。微阵列数据显示,与N22相比,Q4359中差异表达的基因比Q4646更多。Q4646和N22之间不同的大多数基因在Q4359和N22之间也存在差异。对Q4359和Q4646中差异表达基因的GO分析表明,一些基因如淀粉生物合成相关基因受到抑制,而碳水化合物代谢等代谢基因在Q4359和Q4646种子中相对于N22增强。一些参与细胞氧化还原稳态和染色质重塑的基因表达仅在Q4359和N22之间存在显著差异。结果表明细胞氧化还原稳态、染色质重塑与种子休眠之间存在密切相关性。此外,一些参与ABA信号传导的基因被下调,一些参与GA生物合成和信号传导的基因被上调。这些观察结果表明,Q4359种子休眠降低是由ABA-GA拮抗作用调控的。少数差异表达基因位于包含qSdn-1和qSdn-5的区域,表明它们可能是种子休眠的潜在候选基因。我们的工作为进一步确定种子休眠的潜在机制以及从N22中克隆种子休眠基因提供了有用线索。