Overexpression of two DELLA subfamily genes MiSLR1 and MiSLR2 from mango promotes early flowering and enhances abiotic stress tolerance in Arabidopsis

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Plant Science Pub Date : 2024-09-05 DOI:10.1016/j.plantsci.2024.112242
Ziyi Yang, Bingbing Huo, Songjie Wei, Wei Zhang, Xiuxia He, Jiaqi Liang, Siyu Nong, Tianli Guo, Xinhua He, Cong Luo
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Abstract

Gibberellic acids (GAs) are a group of endogenous phytohormones that play important roles in plant growth and development. SLENDER RICE (SLR) serves as a vital component of the DELLA gene family, which plays an irreplaceable role in regulating plant flowering and height, as well as stress responses. SLR gene has not been reported in mango, and its function is unknown. In present study, two DELLA subfamily genes MiSLR1 and MiSLR2 were identified from mango. MiSLR1 and MiSLR2 were highly expressed in the stems of the juvenile stage, but were expressed at a low level in flower buds and flowers. Gibberellin treatment could up-regulate the expression of MiSLR1 and MiSLR2 genes, but gibberellin biosynthesis inhibitor prohexadione-calcium (Pro-Ca) and paclobutrazol (PAC) treatments significantly down-regulated the expression of MiSLR1, while MiSLR2 was up-regulated. The expression levels of MiSLR1 and MiSLR2 were up-regulated under both salt and drought treatments. Overexpression of MiSLR1 and MiSLR2 genes significantly resulted early flowering in transgenic Arabidopsis and significantly up-regulated the expression levels of endogenous flower-related genes, such as SUPPRESSOR OF CONSTANS1 (SOC1), APETALA1 (AP1), and FRUITFULL (FUL). Interestingly, MiSLR1 significantly reduced the height of transgenic plants, while MiSLR2 gene increased. Overexpression of MiSLR1 and MiSLR2 increased seed germination rate, root length and survival rate of transgenic plants under salt and drought stress. Physiological and biochemical detection showed that the contents of proline (Pro) and superoxide dismutase (SOD) were significantly increased, while the contents of malondialdehyde (MDA) and H2O2 were significantly decreased. Additionally, protein interaction analysis revealed that MiSLR1 and MiSLR2 interacted with several flowering-related and GA-related proteins. The interaction between MiSLR with MiGF14 and MiSOC1 proteins was found for the first time. Taken together, the data showed that MiSLR1 and MiSLR2 in transgenic Arabidopsis both regulated the flowering time and plant height, while also acting as positive regulators of abiotic stress responses.

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过量表达芒果中的两个 DELLA 亚家族基因 MiSLR1 和 MiSLR2 可促进拟南芥无花开花并增强其对非生物胁迫的耐受性。
赤霉素(GA)是一类内源植物激素,在植物生长和发育过程中发挥着重要作用。SLENDER RICE(SLR)是 DELLA 基因家族的重要组成部分,在调控植物开花和高度以及胁迫反应方面发挥着不可替代的作用。SLR 基因在芒果中尚未见报道,其功能也尚不清楚。本研究从芒果中发现了两个 DELLA 亚家族基因 MiSLR1 和 MiSLR2。MiSLR1和MiSLR2在幼果期的茎中高表达,但在花芽和花中表达水平较低。赤霉素处理能上调MiSLR1和MiSLR2基因的表达,但赤霉素生物合成抑制剂丙六酮-钙(Pro-Ca)和吡唑醚菌酯(PAC)处理能显著下调MiSLR1的表达,而上调MiSLR2的表达。在盐和干旱处理下,MiSLR1 和 MiSLR2 的表达水平均上调。过表达 MiSLR1 和 MiSLR2 基因会显著导致转基因拟南芥提前开花,并显著上调内源花相关基因的表达水平,如 CONSTANS1抑制因子(SOC1)、APETALA1(AP1)和 FRUITFULL(FUL)。有趣的是,MiSLR1 基因明显降低了转基因植株的高度,而 MiSLR2 基因则有所增加。过表达 MiSLR1 和 MiSLR2 能提高转基因植株在盐胁迫和干旱胁迫下的种子发芽率、根长和存活率。生理生化检测表明,脯氨酸(Pro)和超氧化物歧化酶(SOD)的含量显著增加,而丙二醛(MDA)和 H2O2 的含量显著降低。此外,蛋白质相互作用分析表明,MiSLR1 和 MiSLR2 与多种开花相关蛋白和 GA 相关蛋白相互作用。首次发现了 MiSLR 与 MiGF14 和 MiSOC1 蛋白的相互作用。总之,研究数据表明,转基因拟南芥中的 MiSLR1 和 MiSLR2 既调控开花时间和植株高度,同时也是非生物胁迫响应的正调控因子。
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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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