对珍珠粟(Pennisetum glaucum)盐胁迫响应的分子认识:途径、差异表达基因和转录因子

Faten Dhawi
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摘要

引言 珍珠粟(Pennisetum glaucum)作为一种谷类作物在干旱和半干旱地区发挥着至关重要的作用,它面临着盐胁迫的严峻挑战。 材料与方法 为了揭示支撑其抗盐胁迫能力的潜在分子机制,我们将 14 天大的幼苗分为三组:对照组、75 mM NaCl 组和 150 mM NaCl 组。在为期 7 天的时间里,这些花盆每天都接受各自处理溶液的灌溉。经过一周的处理后,我们测量了植物的叶绿素含量以及芽和根的鲜重和干重。结果表明,与对照组相比,盐水处理(尤其是 150 mM NaCl 组)对重量和叶绿素含量的影响更为明显,超过了在 75 mM NaCl 组观察到的效果。随后,我们对对照组和 150 mM NaCl 处理组的珍珠米叶片进行了 RNA 序列分析。 结果表明,与对照组相比,27.6%的珍珠粟基因表现出差异表达,其中 3246 个基因上调,7408 个基因下调。主成分分析强调了对照组和盐胁迫组之间基因表达模式的明显差异。通路分析揭示了上调的差异表达基因(DEGs),突出表明它们参与了phytyl-PP 生物合成、赖氨酸降解、谷氨酸生物合成、硝酸盐同化和 DLO 生物合成等关键通路。相反,下调的 DEGs 与香豆素生物合成、蒎烷醇生物合成、UDP-d-葡萄糖醛酸生物合成和胆固醇生物合成等途径有关。此外,我们的转录因子分析揭示了与盐胁迫反应相关的特定家族,包括 bHLH、ERF、NAC、WRKY、bZIP、MYB 和 HD-ZIP。 结论 这些发现标志着我们在理解珍珠粟抵御盐胁迫能力方面取得了重大进展,并为开发抗盐作物提供了潜在目标,有助于促进受盐碱影响地区的可持续农业发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Molecular insights into the salt stress response of Pearl millet (Pennisetum glaucum): Pathways, differentially expressed genes and transcription factors

Introduction

Pearl millet (Pennisetum glaucum) plays a crucial role as a cereal crop in arid and semi-arid regions, where it confronts the formidable challenge of salt stress.

Materials and Methods

To unravel the underlying molecular mechanisms that underpin its salt stress resilience, we subjected 14-day-old seedlings to three distinct groups: Control, 75 mM NaCl and 150 mM NaCl. These pots received daily irrigation with their respective treatment solutions for a duration of 7 days. Following this week-long treatment, we measured plant chlorophyll content, as well as the fresh and dry weights of shoots and roots. It became evident that the saline treatment, particularly in the 150 mM NaCl group, had a more pronounced impact on both weight and chlorophyll content in comparison to the control group, surpassing the effects observed in the 75 mM NaCl group. Subsequently, we conducted RNA sequence analysis on the leaves of Pearl millet from both the control and 150 mM NaCl-treated groups.

Results

The results revealed that 27.6% of Pennisetum glaucum genes exhibited differential expression, with 3246 genes being upregulated and 7408 genes downregulated when compared to the control group. Principal component analysis underscored distinct variations in gene expression patterns between the control and salt-stressed groups. Pathway analysis sheds light on the upregulated differentially expressed genes (DEGs), highlighting their involvement in crucial pathways such as phytyl-PP biosynthesis, lysine degradation, glutamate biosynthesis, nitrate assimilation and DLO biosynthesis. Conversely, the downregulated DEGs were associated with pathways like coumarins biosynthesis, pinobanksin biosynthesis, UDP- d-glucuronate biosynthesis and cholesterol biosynthesis, among others. Furthermore, our transcription factor analysis unveiled specific families associated with the salt stress response, including bHLH, ERF, NAC, WRKY, bZIP, MYB and HD-ZIP.

Conclusions

These findings represent a significant advancement in our comprehension of Pearl millet's capacity to withstand salt stress and provide potential targets for the development of salt-resistant crops, contributing to the advancement of sustainable agriculture in regions affected by salinity.

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