Growth-regulating factor 15-mediated vascular cambium differentiation positively regulates wood formation in hybrid poplar (Populus alba × P. glandulosa)

IF 4.1 2区 生物学 Q1 PLANT SCIENCES Frontiers in Plant Science Pub Date : 2024-02-15 DOI:10.3389/fpls.2024.1343312
Houjun Zhou, Xueqin Song, Meng-Zhu Lu
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Abstract

IntroductionHybrid poplars are industrial trees in China. An understanding of the molecular mechanism underlying wood formation in hybrid poplars is necessary for molecular breeding. Although the division and differentiation of vascular cambial cells is important for secondary growth and wood formation, the regulation of this process is largely unclear.MethodsIn this study, mPagGRF15 OE and PagGRF15-SRDX transgenic poplars were generated to investigate the function of PagGRF15. RNA-seq and qRT-PCR were conducted to analyze genome-wide gene expression, while ChIP‒seq and ChIP-PCR were used to identified the downstream genes regulated by PagGRF15.Results and discussionWe report that PagGRF15 from hybrid poplar (Populus alba × P. glandulosa), a growth-regulating factor, plays a critical role in the regulation of vascular cambium activity. PagGRF15 was expressed predominantly in the cambial zone of vascular tissue. Overexpression of mPagGRF15 (the mutated version of GRF15 in the miR396 target sequence) in Populus led to decreased plant height and internode number. Further stem cross sections showed that the mPagGRF15 OE plants exhibited significant changes in vascular pattern with an increase in xylem and a reduction in phloem. In addition, cambium cell files were decreased in the mPagGRF15 OE plants. However, dominant suppression of the downstream genes of PagGRF15 using PagGRF15-SRDX showed an opposite phenotype. Based on the RNA-seq and ChIP-seq results, combining qRT-PCR and ChIP-PCR analysis, candidate genes, such as WOX4b, PXY and GID1.3, were obtained and found to be mainly involved in cambial activity and xylem differentiation. Accordingly, we speculated that PagGRF15 functions as a positive regulator mediating xylem differentiation by repressing the expression of the WOX4a and PXY genes to set the pace of cambial activity. In contrast, PagGRF15 mediated the GA signaling pathway by upregulating GID1.3 expression to stimulate xylem differentiation. This study provides valuable information for further studies on vascular cambium differentiation mechanisms and genetic improvement of the specific gravity of wood in hybrid poplars.
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生长调节因子 15 介导的维管束分化对杂交杨(白杨×腺杨)木材的形成具有积极的调节作用
引言杂交杨树是中国的工业树种。了解杂交杨树木材形成的分子机制对于分子育种非常必要。本研究通过mPagGRF15 OE和PagGRF15-SRDX转基因杨树来研究PagGRF15的功能。结果与讨论我们发现杂交杨树(Populus alba × P. glandulosa)中的 PagGRF15 是一种生长调节因子,在调控维管束韧皮部活性中起着关键作用。PagGRF15 主要在维管组织的韧皮部表达。在杨树中过表达 mPagGRF15(miR396 目标序列中 GRF15 的突变版本)会导致植株高度和节间数下降。进一步的茎横切面显示,mPagGRF15 OE 植物的维管形态发生了显著变化,木质部增加,韧皮部减少。此外,在 mPagGRF15 OE 植物中,骨架细胞档也有所减少。然而,使用 PagGRF15-SRDX 对 PagGRF15 的下游基因进行显性抑制却显示出相反的表型。根据 RNA-seq 和 ChIP-seq 的结果,结合 qRT-PCR 和 ChIP-PCR 分析,我们得到了候选基因,如 WOX4b、PXY 和 GID1.3,并发现它们主要参与骨皮层活性和木质部分化。因此,我们推测 PagGRF15 是通过抑制 WOX4a 和 PXY 基因的表达来调控木质部分化的速度,从而起到正向调节的作用。相反,PagGRF15通过上调GID1.3的表达来刺激木质部分化,从而介导GA信号通路。这项研究为进一步研究杨树维管束分化机制和杂交杨树木材比重的遗传改良提供了宝贵的信息。
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来源期刊
Frontiers in Plant Science
Frontiers in Plant Science PLANT SCIENCES-
CiteScore
7.30
自引率
14.30%
发文量
4844
审稿时长
14 weeks
期刊介绍: In an ever changing world, plant science is of the utmost importance for securing the future well-being of humankind. Plants provide oxygen, food, feed, fibers, and building materials. In addition, they are a diverse source of industrial and pharmaceutical chemicals. Plants are centrally important to the health of ecosystems, and their understanding is critical for learning how to manage and maintain a sustainable biosphere. Plant science is extremely interdisciplinary, reaching from agricultural science to paleobotany, and molecular physiology to ecology. It uses the latest developments in computer science, optics, molecular biology and genomics to address challenges in model systems, agricultural crops, and ecosystems. Plant science research inquires into the form, function, development, diversity, reproduction, evolution and uses of both higher and lower plants and their interactions with other organisms throughout the biosphere. Frontiers in Plant Science welcomes outstanding contributions in any field of plant science from basic to applied research, from organismal to molecular studies, from single plant analysis to studies of populations and whole ecosystems, and from molecular to biophysical to computational approaches. Frontiers in Plant Science publishes articles on the most outstanding discoveries across a wide research spectrum of Plant Science. The mission of Frontiers in Plant Science is to bring all relevant Plant Science areas together on a single platform.
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