Li Xiao-Jing, Guo Xie, Zhou Yan-Hong, Shi Kai, Zhou Jie, Yu Jing-Quan, Xia Xiao-Jian
Department of Horticulture, Zijingang Campus, Zhejiang University, Hangzhou, 310058, P.R. China.
Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Hangzhou, 310058, China.
BMC Plant Biol. 2016 Jan 28;16:33. doi: 10.1186/s12870-016-0715-6.
Genetic manipulation of brassinosteroid (BR) biosynthesis or signaling is a promising strategy to improve crop yield and quality. However, the relationships between the BR-promoted growth and photosynthesis and the exact mechanism of BR-regulated photosynthetic capacity are not clear. Here, we generated transgenic tomato plants by overexpressing Dwarf, a BR biosynthetic gene that encodes the CYP85A1, and compared the photosynthetic capacity with the BR biosynthetic mutant d (im) and wild type.
Overexpression of Dwarf promoted net photosynthetic rate (P N), whereas BR deficiency in d (im) led to a significant inhibition in P N as compared with WT. The activation status of RuBisCO, and the protein content and activity of RuBisCO activase, but not the total content and transcripts of RuBisCO were closely related to the endogenous BR levels in different genotypes. However, endogenous BR positively regulated the expression and activity of fructose-1,6-bisphosphatase. Dwarf overexpression enhanced the activity of dehydroascorbate reductase and glutathione reductase, leading to a reduced redox status, whereas BR deficiency had the contrasting effects. In addition, BR induced a reduction of 2-cystein peroxiredoxin without altering the protein content.
BR plays a role in the regulation of photosynthesis. BR can increase the photosynthetic capacity by inducing a reduced redox status that maintains the activation states of Calvin cycle enzymes.
对油菜素内酯(BR)生物合成或信号传导进行基因操作是提高作物产量和品质的一种有前景的策略。然而,BR促进生长与光合作用之间的关系以及BR调节光合能力的确切机制尚不清楚。在此,我们通过过表达Dwarf(一个编码CYP85A1的BR生物合成基因)生成了转基因番茄植株,并将其光合能力与BR生物合成突变体d(im)和野生型进行了比较。
Dwarf的过表达促进了净光合速率(P N),而与野生型相比,d(im)中BR缺乏导致P N显著抑制。核酮糖-1,5-二磷酸羧化酶/加氧酶(RuBisCO)的激活状态、RuBisCO活化酶的蛋白质含量和活性,而非RuBisCO的总含量和转录本,与不同基因型中的内源BR水平密切相关。然而,内源BR正向调节果糖-1,6-二磷酸酶的表达和活性。Dwarf过表达增强了脱氢抗坏血酸还原酶和谷胱甘肽还原酶的活性,导致氧化还原状态降低,而BR缺乏则产生相反的效果。此外,BR诱导2-半胱氨酸过氧化物酶减少,但不改变蛋白质含量。
BR在光合作用调节中发挥作用。BR可通过诱导降低的氧化还原状态来维持卡尔文循环酶的激活状态,从而提高光合能力。