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木质部特异性 SND5 及其同源物通过激活次生壁 NAC 结合元件来调节次生壁生物合成。

Xylem vessel-specific SND5 and its homologs regulate secondary wall biosynthesis through activating secondary wall NAC binding elements.

机构信息

Department of Plant Biology, University of Georgia, Athens, GA, 30602, USA.

Department of Plant & Environmental New Resources, College of Life Sciences, Kyung Hee University, Yongin, 17104, Republic of Korea.

出版信息

New Phytol. 2021 Aug;231(4):1496-1509. doi: 10.1111/nph.17425. Epub 2021 Jun 18.

Abstract

Secondary cell wall biosynthesis has been shown to be regulated by a suite of transcription factors. Here, we identified a new xylem vessel-specific NAC domain transcription factor, secondary wall-associated NAC domain protein5 (SND5), in Arabidopsis thaliana and studied its role in regulating secondary wall biosynthesis. We showed that the expression of SND5 and its close homolog, SND4/ANAC075, was specifically associated with secondary wall-containing cells and dominant repression of their functions severely reduced secondary wall thickening in these cells. Overexpression of SND4/5 as well as their homologs SND2/3 fused with the activation domain of the viral protein VP16 led to ectopic secondary wall deposition in cells that are normally parenchymatous. SND2/3/4/5 regulated the expression of the same downstream target genes as do the secondary wall NAC master switches (SWNs) by binding to and activating the secondary wall NAC binding elements (SNBEs). Furthermore, we demonstrated that the poplar (Populus trichocarpa) orthologs of SND2/3/4/5 also activated SNBEs and regulated secondary wall biosynthesis during wood formation. Together, these findings indicate that SND2/3/4/5 and their poplar orthologs regulate the expression of secondary wall-associated genes through activating SNBEs and they are positioned at an upper level in the SWN-mediated transcriptional network.

摘要

次生细胞壁生物合成已被证明受到一系列转录因子的调控。在这里,我们在拟南芥中鉴定了一个新的木质部导管特异性 NAC 结构域转录因子,次生壁相关 NAC 结构域蛋白 5(SND5),并研究了它在调节次生壁生物合成中的作用。我们表明,SND5 及其密切同源物 SND4/ANAC075 的表达与含有次生壁的细胞特异性相关,其功能的显性抑制严重降低了这些细胞中次生壁的增厚。SND4/5 的过表达及其与病毒蛋白 VP16 的激活结构域融合的同源物 SND2/3 导致在通常是薄壁组织的细胞中外生的次生壁沉积。SND2/3/4/5 通过与次生壁 NAC 结合元件(SNBEs)结合并激活 SNBEs,调节与次生壁 NAC 主开关(SWNs)相同的下游靶基因的表达。此外,我们证明杨树(Populus trichocarpa)的 SND2/3/4/5 同源物也激活 SNBEs 并在木质部形成过程中调节次生壁生物合成。总之,这些发现表明 SND2/3/4/5 及其杨树同源物通过激活 SNBEs 调节次生壁相关基因的表达,并且它们在 SWN 介导的转录网络中处于较高水平。

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