{"title":"Growth-regulating factor 15-mediated vascular cambium differentiation positively regulates wood formation in hybrid poplar (Populus alba × P. glandulosa)","authors":"Houjun Zhou, Xueqin Song, Meng-Zhu Lu","doi":"10.3389/fpls.2024.1343312","DOIUrl":null,"url":null,"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, <jats:italic>mPagGRF15</jats:italic> OE and <jats:italic>PagGRF15-SRDX</jats:italic> transgenic poplars were generated to investigate the function of <jats:italic>PagGRF15</jats:italic>. 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 <jats:italic>PagGRF15</jats:italic>.Results and discussionWe report that <jats:italic>PagGRF15</jats:italic> from hybrid poplar (<jats:italic>Populus alba</jats:italic> × <jats:italic>P. glandulosa</jats:italic>), a growth-regulating factor, plays a critical role in the regulation of vascular cambium activity. <jats:italic>PagGRF15</jats:italic> was expressed predominantly in the cambial zone of vascular tissue. Overexpression of <jats:italic>mPagGRF15</jats:italic> (the mutated version of <jats:italic>GRF15</jats:italic> in the <jats:italic>miR396</jats:italic> target sequence) in Populus led to decreased plant height and internode number. Further stem cross sections showed that the <jats:italic>mPagGRF15</jats:italic> 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 <jats:italic>mPagGRF15</jats:italic> OE plants. However, dominant suppression of the downstream genes of <jats:italic>PagGRF15</jats:italic> using <jats:italic>PagGRF15-SRDX</jats:italic> showed an opposite phenotype. Based on the RNA-seq and ChIP-seq results, combining qRT-PCR and ChIP-PCR analysis, candidate genes, such as <jats:italic>WOX4b</jats:italic>, <jats:italic>PXY</jats:italic> and <jats:italic>GID1.3</jats:italic>, were obtained and found to be mainly involved in cambial activity and xylem differentiation. Accordingly, we speculated that <jats:italic>PagGRF15</jats:italic> functions as a positive regulator mediating xylem differentiation by repressing the expression of the <jats:italic>WOX4a</jats:italic> and <jats:italic>PXY</jats:italic> genes to set the pace of cambial activity. In contrast, <jats:italic>PagGRF15</jats:italic> mediated the GA signaling pathway by upregulating <jats:italic>GID1.3</jats:italic> 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.","PeriodicalId":12632,"journal":{"name":"Frontiers in Plant Science","volume":null,"pages":null},"PeriodicalIF":4.1000,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Plant Science","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fpls.2024.1343312","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
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.
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.