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1
Non-cell-autonomous postmortem lignification of tracheary elements in Zinnia elegans.Zinnia elegans 导管分子的非细胞自主死后木质化。
Plant Cell. 2013 Apr;25(4):1314-28. doi: 10.1105/tpc.113.110593. Epub 2013 Apr 9.
2
A mechanism for localized lignin deposition in the endodermis.在内皮层中局部木质素沉积的机制。
Cell. 2013 Apr 11;153(2):402-12. doi: 10.1016/j.cell.2013.02.045. Epub 2013 Mar 28.
3
Engineering secondary cell wall deposition in plants.在植物中工程化次生细胞壁的沉积。
Plant Biotechnol J. 2013 Apr;11(3):325-35. doi: 10.1111/pbi.12016. Epub 2012 Nov 12.
4
Impact of the absence of stem-specific β-glucosidases on lignin and monolignols.缺乏木质素特异性β-葡萄糖苷酶对木质素和单体酚的影响。
Plant Physiol. 2012 Nov;160(3):1204-17. doi: 10.1104/pp.112.203364. Epub 2012 Sep 14.
5
Plant cell biology: the ABC of monolignol transport.植物细胞生物学:木质素单体运输的 ABC 。
Curr Biol. 2012 Jul 10;22(13):R533-5. doi: 10.1016/j.cub.2012.05.005.
6
AtABCG29 is a monolignol transporter involved in lignin biosynthesis.ABCG29 是一种参与木质素生物合成的单酚转运蛋白。
Curr Biol. 2012 Jul 10;22(13):1207-12. doi: 10.1016/j.cub.2012.04.064. Epub 2012 Jun 14.
7
Casparian strip diffusion barrier in Arabidopsis is made of a lignin polymer without suberin.拟南芥中的凯氏带扩散屏障由木质素聚合物构成,不含栓质体。
Proc Natl Acad Sci U S A. 2012 Jun 19;109(25):10101-6. doi: 10.1073/pnas.1205726109. Epub 2012 Jun 4.
8
Disruption of LACCASE4 and 17 results in tissue-specific alterations to lignification of Arabidopsis thaliana stems.LACCASE4 和 17 的缺失导致拟南芥茎木质化的组织特异性改变。
Plant Cell. 2011 Mar;23(3):1124-37. doi: 10.1105/tpc.110.082792. Epub 2011 Mar 29.
9
Cell-specific chemotyping and multivariate imaging by combined FT-IR microspectroscopy and orthogonal projections to latent structures (OPLS) analysis reveals the chemical landscape of secondary xylem.利用傅里叶变换红外显微光谱结合正交投影到潜在结构(OPLS)分析进行细胞特异性化学分型和多元成像揭示了次生木质部的化学特征。
Plant J. 2011 Jun;66(5):903-14. doi: 10.1111/j.1365-313X.2011.04542.x. Epub 2011 Mar 21.
10
Sequestration and transport of lignin monomeric precursors.木质素单体前体的隔离和运输。
Molecules. 2011 Jan 18;16(1):710-27. doi: 10.3390/molecules16010710.

邻近的实质细胞有助于拟南芥木质部的木质化,而束间纤维的木质化是细胞自主的。

Neighboring parenchyma cells contribute to Arabidopsis xylem lignification, while lignification of interfascicular fibers is cell autonomous.

机构信息

Department of Botany, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.

出版信息

Plant Cell. 2013 Oct;25(10):3988-99. doi: 10.1105/tpc.113.117176. Epub 2013 Oct 4.

DOI:10.1105/tpc.113.117176
PMID:24096341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3877792/
Abstract

Lignin is a critical structural component of plants, providing vascular integrity and mechanical strength. Lignin precursors (monolignols) must be exported to the extracellular matrix where random oxidative coupling produces a complex lignin polymer. The objectives of this study were twofold: to determine the timing of lignification with respect to programmed cell death and to test if nonlignifying xylary parenchyma cells can contribute to the lignification of tracheary elements and fibers. This study demonstrates that lignin deposition is not exclusively a postmortem event, but also occurs prior to programmed cell death. Radiolabeled monolignols were not detected in the cytoplasm or vacuoles of tracheary elements or neighbors. To experimentally define which cells in lignifying tissues contribute to lignification in intact plants, a microRNA against cinnamoyl CoA-reductase1 driven by the promoter from cellulose synthase7 (ProCESA7:miRNA CCR1) was used to silence monolignol biosynthesis specifically in cells developing lignified secondary cell walls. When monolignol biosynthesis in ProCESA7:miRNA CCR1 lines was silenced in the lignifying cells themselves, but not in the neighboring cells, lignin was still deposited in the xylem secondary cell walls. Surprisingly, a dramatic reduction in cell wall lignification of extraxylary fiber cells demonstrates that extraxylary fibers undergo cell autonomous lignification.

摘要

木质素是植物的重要结构组成部分,提供了维管束的完整性和机械强度。木质素前体(单酚)必须被运出到细胞外基质,在那里随机氧化偶联产生复杂的木质素聚合物。本研究的目的有两个:确定木质化与程序性细胞死亡的时间关系,并测试非木质化木质部薄壁细胞是否可以促进导管分子和纤维的木质化。本研究表明,木质素的沉积不仅是死后事件,也发生在程序性细胞死亡之前。放射性标记的单酚在导管分子或其相邻细胞的细胞质或液泡中未被检测到。为了在完整植物中实验性地定义木质化组织中的哪些细胞有助于木质化,使用由纤维素合酶 7(ProCESA7)启动子驱动的针对肉桂酰辅酶 A 还原酶 1(cinnamoyl CoA-reductase1)的 microRNA(ProCESA7:miRNA CCR1)来沉默专门在木质化次生细胞壁发育中的细胞中单酚的生物合成。当 ProCESA7:miRNA CCR1 系中的单酚生物合成在木质化细胞中被沉默,但不在相邻细胞中被沉默时,木质素仍被沉积在木质部次生细胞壁中。令人惊讶的是,外生纤维细胞细胞壁木质素的急剧减少表明外生纤维细胞经历了细胞自主木质化。