NST3 induces ectopic transdifferentiation, forming secondary walls with diverse patterns and composition in Arabidopsis thaliana.

IF 3.6 2区 生物学 Q1 PLANT SCIENCES Annals of botany Pub Date : 2024-08-30 DOI:10.1093/aob/mcae153
Chetana Tamadaddi, Juseok Choi, Masoud Ghasemi, Seong H Kim, Enrique D Gomez, Esther W Gomez, Charles T Anderson
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Abstract

Background and aims: The master transcription factor NAC SECONDARY WALL THICKENING PROMOTING FACTOR3 (NST3), also known as SND1, plays a pivotal role in regulating secondary cell wall (SCW) development in interfascicular and xylary fibers in Arabidopsis thaliana. Despite progress in understanding SCW assembly in xylem vessel-like cells, the mechanisms behind its assembly across different cell types remain unclear. Overexpressing NST3 or its homolog NST1 leads to reduced fertility, posing challenges for studying their impact on secondary wall formation. This study aimed at developing a tightly regulated dexamethasone (DEX)-inducible expression system for NST3 and NST1 to elucidate the structure and assembly of diverse SCWs.

Methods: Using the DEX-inducible system, we characterized ectopically formed SCWs for their diverse patterns, mesoscale organization, cellulose microfibril orientation, and molecular composition using spinning disk confocal microscopy, field emission scanning electron microscopy (FESEM), vibrational sum-frequency generation (SFG) spectroscopy and, histochemical staining and time-of-flight secondary ion mass spectrometry (ToF-SIMS), respectively.

Key results: Upon DEX treatment, NST3 and NST1 transgenic hypocotyls underwent time-dependent transdifferentiation, progressing from protoxylem-like to metaxylem-like cells. NST3-induced plants exhibited normal growth but had rough secondary wall surfaces with delaminating S2 and S3 layers. Mesoscale examination of induced SCWs in epidermal cells revealed that macrofibril thickness and orientation were comparable to xylem vessels, while wall thickness resembled that of interfascicular fibers. Additionally, induced epidermal cells formed SCWs with altered cellulose and lignin contents.

Conclusions: These findings suggest NST3 and/or NST1 induce SCWs with shared characteristics of both xylem and fiber-like cells forming loosely arranged cell wall layers and cellulose organized at multiple angles relative to the cell growth axis and with varied cellulose and lignin abundance. This inducible system opens avenues to explore ectopic SCWs for bioenergy and bioproducts, offering valuable insights into SCW patterning across diverse cell types and developmental stages.

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NST3 可诱导拟南芥异位转分化,形成具有不同模式和组成的次生壁。
背景和目的:主转录因子 NAC 次级细胞壁增厚促进因子3 (NST3),又称 SND1,在调节拟南芥束间纤维和木质纤维的次级细胞壁(SCW)发育中起着关键作用。尽管在了解木质部血管样细胞中的 SCW 组装方面取得了进展,但其在不同细胞类型中的组装机制仍不清楚。过量表达 NST3 或其同源物 NST1 会导致繁殖力降低,这给研究它们对次生壁形成的影响带来了挑战。本研究旨在开发一种严格调控的地塞米松(DEX)诱导的NST3和NST1表达系统,以阐明不同SCW的结构和组装:方法:利用DEX诱导系统,我们分别使用旋转盘共焦点显微镜、场发射扫描电子显微镜(FESEM)、振动总频发生光谱(SFG)、组织化学染色和飞行时间二次离子质谱(ToF-SIMS)对异位形成的SCWs的不同形态、中尺度组织、纤维素微纤维取向和分子组成进行了表征:主要结果:经DEX处理后,NST3和NST1转基因下胚轴发生了时间依赖性的转分化,从原木质部样细胞转变为中木质部样细胞。NST3 诱导的植株生长正常,但其次生壁表面粗糙,S2 和 S3 层分层。对表皮细胞中的诱导 SCW 进行中尺度检查后发现,大纤维的厚度和取向与木质部血管相当,而壁厚度则与层间纤维相似。此外,诱导表皮细胞形成的SCW的纤维素和木质素含量也发生了变化:这些发现表明,NST3和/或NST1诱导的SCW具有木质部细胞和纤维样细胞的共同特征,即形成松散排列的细胞壁层和相对于细胞生长轴呈多角度排列的纤维素,且纤维素和木质素的丰度各不相同。这种诱导系统为探索生物能源和生物产品的异位SCW开辟了途径,为了解不同细胞类型和发育阶段的SCW形态提供了宝贵的信息。
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来源期刊
Annals of botany
Annals of botany 生物-植物科学
CiteScore
7.90
自引率
4.80%
发文量
138
审稿时长
3 months
期刊介绍: Annals of Botany is an international plant science journal publishing novel and rigorous research in all areas of plant science. It is published monthly in both electronic and printed forms with at least two extra issues each year that focus on a particular theme in plant biology. The Journal is managed by the Annals of Botany Company, a not-for-profit educational charity established to promote plant science worldwide. The Journal publishes original research papers, invited and submitted review articles, ''Research in Context'' expanding on original work, ''Botanical Briefings'' as short overviews of important topics, and ''Viewpoints'' giving opinions. All papers in each issue are summarized briefly in Content Snapshots , there are topical news items in the Plant Cuttings section and Book Reviews . A rigorous review process ensures that readers are exposed to genuine and novel advances across a wide spectrum of botanical knowledge. All papers aim to advance knowledge and make a difference to our understanding of plant science.
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