Populus PtrbHLH011 Is a Transcriptional Co-Regulator Involved in the Activation of Cell Wall Biosynthesis by Iron Deprivation

杨树 PtrbHLH011 是一种转录共调节因子,参与铁缺乏激活细胞壁生物合成。

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作者:Dimiru Tadesse ,Yuqiu Dai ,Gen Li ,Lin Yang ,Yang Yang ,Nidhi Dwivedi ,Desigan Kumaran ,Crysten E Blaby-Haas ,Anna Lipzen ,Kassandra Santiago ,Kerrie Barry ,Gary Coleman ,Yiping Qi ,Chang-Jun Liu ,Meng Xie

Abstract

The lack of a mechanistic understanding of the environmental plasticity of secondary cell wall (SCW) biosynthesis restricts large-scale biomass and bioenergy production on marginal lands. Using Populus (poplar), a key bioenergy crop, we discovered that iron deprivation, a prevalent abiotic stress on marginal lands, stimulates SCW biosynthesis in stems. We identified the transcription factor PtrbHLH011 as a critical regulator underlying this response. Through integrated analyses involving phenotypic characterisation of PtrbHLH011 knockout and overexpression plants, functional genomics and molecular investigations, we established that PtrbHLH011 functions as a central regulator of SCW biosynthesis, iron homeostasis and flavonoid biosynthesis by directly repressing essential genes in these pathways. Iron deprivation downregulates PtrbHLH011 expression, subsequently activating these biosynthetic pathways. Notably, cytosine base editing-based knockout of PtrbHLH011 significantly enhanced plant growth, yielding up to a 110% increase in stem diameter and a 300% increase in leaf iron content. These findings present a novel regulatory mechanism linking environmental iron availability to SCW biosynthesis and illustrate a practical strategy to improve biomass yield on iron-deficient marginal lands. Furthermore, our mechanistic insights into PtrbHLH011 target recognition and regulation provide a valuable foundation for precise manipulation of gene regulatory networks, facilitating the development of high-performance bioenergy crops adapted to marginal environments. Keywords: bioenergy; growth enhance; iron homeostasis; marginal lands; poplar; secondary cell wall; transcriptional co‐regulation.

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