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红松转录组分析鉴定了与次生细胞壁形成相关的关键基因和参与导管形成的 NAC 转录因子。

Wood transcriptome analysis of Pinus densiflora identifies genes critical for secondary cell wall formation and NAC transcription factors involved in tracheid formation.

机构信息

Department of Plant & Environmental New Resources, Kyung Hee University, 1732 Deogyeong-daero, Yongin 17104, Republic of Korea.

Division of Forest Biotechnology, National Institute of Forest Science, 39 Onjeong-ro, Suwon 16631, Republic of Korea.

出版信息

Tree Physiol. 2021 Jul 5;41(7):1289-1305. doi: 10.1093/treephys/tpab001.

Abstract

Although conifers have significant ecological and economic value, information on transcriptional regulation of wood formation in conifers is still limited. Here, to gain insight into secondary cell wall (SCW) biosynthesis and tracheid formation in conifers, we performed wood tissue-specific transcriptome analyses of Pinus densiflora (Korean red pine) using RNA sequencing. In addition, to obtain full-length transcriptome information, PacBio single molecule real-time iso-sequencing was carried out using RNAs from 28 tissues of P. densiflora. Subsequent comparative tissue-specific transcriptome analysis successfully pinpointed critical genes encoding key proteins involved in biosynthesis of the major secondary wall components (cellulose, galactoglucomannan, xylan and lignin). Furthermore, we predicted a total of 62 NAC (NAM, ATAF1/2 and CUC2) family transcription factor members and identified seven PdeNAC genes preferentially expressed in developing xylem tissues in P. densiflora. Protoplast-based transcriptional activation analysis found that four PdeNAC genes, homologous to VND, NST and SND/ANAC075, upregulated GUS activity driven by an SCW-specific cellulose synthase promoter. Consistently, transient overexpression of the four PdeNACs induced xylem vessel cell-like SCW deposition in both tobacco (Nicotiana benthamiana) and Arabidopsis leaves. Taken together, our data provide a foundation for further research to unravel transcriptional regulation of wood formation in conifers, especially SCW formation and tracheid differentiation.

摘要

尽管针叶树具有重要的生态和经济价值,但有关针叶树木质部形成的转录调控信息仍然有限。在这里,为了深入了解针叶树次生细胞壁 (SCW) 的生物合成和管胞形成,我们使用 RNA 测序对赤松 (Korean red pine) 的木质部组织进行了特异性转录组分析。此外,为了获得全长转录组信息,我们使用赤松的 28 种组织的 RNA 进行了 PacBio 单分子实时同聚物测序。随后的比较组织特异性转录组分析成功地确定了关键基因,这些基因编码参与主要次生壁成分(纤维素、半乳糖甘露聚糖、木聚糖和木质素)生物合成的关键蛋白。此外,我们总共预测了 62 个 NAC(NAM、ATAF1/2 和 CUC2)家族转录因子成员,并鉴定了 7 个在赤松发育木质部组织中优先表达的 PdeNAC 基因。基于原生质体的转录激活分析发现,四个 PdeNAC 基因与 VND、NST 和 SND/ANAC075 同源,可上调由 SCW 特异性纤维素合酶启动子驱动的 GUS 活性。一致地,四个 PdeNAC 基因的瞬时过表达在烟草(Nicotiana benthamiana)和拟南芥叶片中诱导了木质部导管细胞样 SCW 沉积。总之,我们的数据为进一步研究针叶树木质部形成的转录调控,特别是 SCW 形成和管胞分化,提供了基础。

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