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缺铁胁迫下转录因子(TF)的功能分析

Functional Analysis of Transcription Factor (TF) Under Iron (Fe) Deficiency Stress.

作者信息

Luo Hongjia, Liu Wenqing, Wang Xiaoya, Wang Yanxiu

机构信息

College of Horticulture, Gansu Agricultural University, Lanzhou 730070, China.

Forestry Technique Extension Station of Gansu Province, Lanzhou 730070, China .

出版信息

Curr Issues Mol Biol. 2025 Jul 21;47(7):576. doi: 10.3390/cimb47070576.

Abstract

Fe deficiency in apple trees can lead to leaf chlorosis and impede root development, resulting in significant alterations in signaling, metabolism, and genetic functions, which severely restricts fruit yield and quality. It is well established that WRKY transcription factors (TFs) are of vital significance in mediating plant responses to abiotic stress. Real-time quantitative fluorescence (RT-qPCR) analysis displayed that Fe deficiency stress can significantly induce TF gene expression. However, the potential mechanisms by which the gene involved in Fe deficiency stress remains to be investigated. To address this limitations, the gene (MD09G1235100) was successfully isolated from apple rootstock and performed both homologous and heterologous expression analyses in apple calli and tobacco to elucidate its functional role in response to Fe deficiency stress. The findings indicated that transgenic tobacco plants exhibited enhanced growth vigor and reduced chlorosis when subjected to Fe deficiency stress compared to the wild type (WT). Additionally, the apple calli that were overexpressed also exhibited superior growth and quality. Furthermore, the overexpression of the gene enhanced the ability of tobacco to Fe deficiency stress tolerance by stimulating the synthesis of photosynthetic pigments, increasing antioxidant enzyme activity, and facilitating Fe reduction. Additionally, it increased the resistance of apple calli to Fe deficiency stress by enhancing Fe reduction and elevating the activity of antioxidant enzymes. For example, under Fe deficiency stress, the proline (Pro) contents of the overexpression lines (OE-2, OE-5, OE-6) were 26.18 mg·g, 26.13 mg·g, and 26.27 mg·g, respectively, which were 16.98%, 16.76%, and 17.38% higher than the proline content of 22.38 mg·g in the wild-type lines, respectively. To summarize, a functional analysis of tobacco plants and apple calli displayed that WRKY69 TF serves as a positive regulator under Fe deficiency stress, which provides candidate genetic resources for cultivating apple rootstocks or varieties with strong stress (Fe deficiency) resistance.

摘要

苹果树缺铁会导致叶片黄化并阻碍根系发育,从而引起信号传导、新陈代谢和基因功能的显著变化,严重限制果实产量和品质。众所周知,WRKY转录因子在介导植物对非生物胁迫的反应中具有至关重要的意义。实时定量荧光(RT-qPCR)分析表明,缺铁胁迫可显著诱导转录因子基因表达。然而,参与缺铁胁迫的基因的潜在机制仍有待研究。为了解决这一局限性,从苹果砧木中成功分离出该基因(MD09G1235100),并在苹果愈伤组织和烟草中进行了同源和异源表达分析,以阐明其在响应缺铁胁迫中的功能作用。研究结果表明,与野生型(WT)相比,转基因烟草植株在缺铁胁迫下表现出更强的生长活力和更少的黄化现象。此外,过表达该基因的苹果愈伤组织也表现出更好的生长和品质。此外,该基因的过表达通过刺激光合色素的合成、增加抗氧化酶活性和促进铁还原,增强了烟草对缺铁胁迫的耐受性。此外,它还通过增强铁还原和提高抗氧化酶活性,增加了苹果愈伤组织对缺铁胁迫的抗性。例如,在缺铁胁迫下,过表达系(OE-2、OE-5、OE-6)的脯氨酸(Pro)含量分别为26.18 mg·g、26.13 mg·g和26.27 mg·g,分别比野生型系中22.38 mg·g的脯氨酸含量高出16.98%、16.76%和17.38%。综上所述,对烟草植株和苹果愈伤组织的功能分析表明,WRKY69转录因子在缺铁胁迫下作为正调控因子,为培育具有强抗逆性(缺铁)的苹果砧木或品种提供了候选遗传资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2be/12293516/f1dd60c1c2f9/cimb-47-00576-g001.jpg

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