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ArNAC148 通过激活 ABA 受体基因 ArPYR13 的转录诱导 Acer rubrum 叶片衰老。

ArNAC148 induces Acer rubrum leaf senescence by activating the transcription of the ABA receptor gene ArPYR13.

机构信息

Institute of Agricultural Engineering, Anhui Academy of Agricultural Sciences, Hefei 230031, China.

Anhui Wenda University of Information Engineering, Anhui Province, Anhui 230032, China.

出版信息

Int J Biol Macromol. 2024 Nov;279(Pt 2):134950. doi: 10.1016/j.ijbiomac.2024.134950. Epub 2024 Sep 1.

Abstract

Acer rubrum, an ornamental tree known for its stunning autumn colors, has an elusive molecular mechanism that governs its leaf senescence. We performed the genome-wide analysis of NAC transcription factor genes and PYRABACTIN RESISTANCE1-LIKE (PYLs) and found that ArNAC148 and ArPYL13 were significantly upregulated in senescing leaves as compared to mature leaves. Subcellular localization studies confirmed the nuclear localization of ArNAC148 and the cytoplasmic localization of ArPYL13. Electrophoretic mobility shift assay and yeast one-hybrid assay demonstrated that ArNAC148 directly binds to the promoter of ArPYL13. Luciferase reporter assays further showed that ArNAC148 activates the transcription of ArPYL13. The transient expression of ArNAC148 and ArPYL13 in tobacco leaves promoted chlorophyll degradation, increased HO level, MDA contents, and electrolyte leakage in response to abscisic acid (ABA). Moreover, the virus-induced gene silencing of ArNAC148 and ArPYL13 in A. rubrum produced results that were opposite to those observed in transient expression experiments. Our findings suggest that ArNAC148 induces leaf senescence by directly activating the transcription of ArPYL13, providing insights into the ABA-mediated regulatory mechanisms governing leaf senescence in A. rubrum. This study offers new perspectives for researchers to explore the roles of NAC and PYL genes in regulating leaf senescence in woody ornamental plants.

摘要

红花槭,一种以其惊艳的秋季色彩而闻名的观赏树种,其叶片衰老的分子机制一直难以捉摸。我们对 NAC 转录因子基因和 PYRABACTIN RESISTANCE1-LIKE(PYLs)进行了全基因组分析,发现与成熟叶片相比,ArNAC148 和 ArPYL13 在衰老叶片中显著上调。亚细胞定位研究证实了 ArNAC148 的核定位和 ArPYL13 的细胞质定位。电泳迁移率变动分析和酵母单杂交实验表明,ArNAC148 可直接结合到 ArPYL13 的启动子上。荧光素酶报告基因实验进一步表明,ArNAC148 激活了 ArPYL13 的转录。瞬时表达烟草叶片中的 ArNAC148 和 ArPYL13 可促进叶绿素降解,增加 HO 水平、MDA 含量和电解质渗漏,对脱落酸(ABA)产生响应。此外,在红花槭中病毒诱导的基因沉默 ArNAC148 和 ArPYL13 的实验结果与瞬时表达实验的观察结果相反。我们的研究结果表明,ArNAC148 通过直接激活 ArPYL13 的转录诱导叶片衰老,为 ABA 介导的红花槭叶片衰老调控机制提供了新的见解。本研究为研究人员探索 NAC 和 PYL 基因在调控木本观赏植物叶片衰老中的作用提供了新的视角。

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