Coordinated chromatin modifications mediated by AREB and MYB transcription factors sustain drought tolerance in Populus.

IF 6.5 1区 生物学 Q1 PLANT SCIENCES
Jinghui Gao,Xiaoqian Wu,Rui Zhai,Huizi Liu,Jinfeng Zhao,Chenguang Zhou,Shuang Li,Wei Li
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引用次数: 0

Abstract

Sustained drought tolerance in plants relies on transcriptional memory through successive stress cycles, yet the chromatin-based mechanisms underlying this memory remain unclear. Previously, we revealed that PtrMYB161 overexpression in Populus trichocarpa results in phenotypes characteristic of drought tolerance. Here, we confirm that such transgenesis instills an epigenetic path to gene transregulation for drought tolerance. PtrMYB161 binds directly to the MYB-core motif in the promoter of PtrNAC120, a drought response/tolerance gene, to recruit the histone acetyltransferase (HAT) dimer GENERAL CONTROL NON-DEREPRESSIBLE5-1-ALTERATION/DEFICIENCY IN ACTIVATION2b-3 (PtrGCN5-1-PtrADA2b-3), forming the ternary protein complex (PtrMYB161-PtrGCN5-1-PtrADA2b-3). This ternary system enables enhanced acetylation of nucleosome histone 3 lysine-9, -14, and -27 (H3K9, H3K14, and H3K27) for enriched RNA Pol II occupancy in the PtrNAC120 promoter to elevate its expression for drought tolerance. Unlike PtrAREB1-2, an important drought-inducible transcription factor that can also mediate PtrNAC120 transactivation for tolerance, PtrMYB161 expression remains unaffected by drought. However, under drought conditions, induced PtrAREB1-2 could form HAT ternary complexes, PtrAREB1-2-PtrGCN5-1-PtrADA2b-3, and bind to PtrAREB1-binding sites (ABREs) in the PtrNAC120 promoter for PtrNAC120's enhanced H3K acetylation, RNA Pol II occupancy, and transactivation for drought tolerance. PtrMYB161-PtrGCN5-1-PtrADA2b-3-mediated PtrNAC120 transactivation was induced following severe, prolonged drought stress (below 40% Relative Soil Water Content) and PtrAREB1-2-induced PtrNAC120 transactivation. Further loss- and gain-of-function transgenesis experiments in whole plants and stem differentiating xylem protoplasts suggest that, under stress, the PtrAREB1-2 regulatory system activates an ancillary regulation mediated by PtrMYB161. Our findings propose coordinated epigenetic regulations mediated by HAT complexes to jointly sustain drought tolerance in Populus.
由AREB和MYB转录因子介导的染色质修饰维持了杨树的抗旱性。
植物的持续耐旱性依赖于通过连续胁迫循环的转录记忆,然而基于染色质的记忆机制尚不清楚。先前,我们发现PtrMYB161在毛杨中过表达导致了耐旱表型特征。在这里,我们证实了这种转基因为耐旱性基因的转调控注入了一条表观遗传途径。PtrMYB161直接与干旱响应/耐受基因PtrNAC120启动子中的myb核心基元结合,募集组蛋白乙酰转移酶(HAT)二聚体GENERAL CONTROL non - deresible5 -1- change / deficient in ACTIVATION2b-3 (PtrGCN5-1-PtrADA2b-3),形成三元蛋白复合物(PtrMYB161-PtrGCN5-1-PtrADA2b-3)。该三元体系能够增强核小体组蛋白3赖氨酸-9、-14和-27 (H3K9、H3K14和H3K27)的乙酰化,从而在PtrNAC120启动子中富集RNA Pol II占用,从而提高其耐旱性表达。与PtrAREB1-2不同,PtrMYB161的表达不受干旱影响。PtrAREB1-2是一种重要的干旱诱导转录因子,也可以介导PtrNAC120的转录激活,从而提高耐受性。然而,在干旱条件下,诱导的PtrAREB1-2可以形成HAT三元配合物,即PtrAREB1-2- ptrgcn5 -1- ptrada2b -3,并与PtrNAC120启动子中的ptrareb1结合位点(ABREs)结合,从而增强PtrNAC120的H3K乙酰化、RNA Pol II占据和转激活,从而获得耐旱性。ptrmyb161 - ptrgcn5 -1- ptrada2b -3介导的PtrNAC120转录激活是在严重、长期干旱胁迫(土壤相对含水量低于40%)和ptrareb1 -2诱导的PtrNAC120转录激活后诱导的。在整个植物和茎分化木质部原生质体中进一步进行的功能丧失和功能获得的转基因实验表明,在逆境下,PtrAREB1-2调控系统激活了由PtrMYB161介导的辅助调控。我们的研究结果表明,由HAT复合物介导的协调表观遗传调控共同维持了杨树的抗旱性。
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
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