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光敏色素互作因子与HECATE蛋白之间的负反馈环精细调控拟南芥的光形态建成。

A Negative Feedback Loop between PHYTOCHROME INTERACTING FACTORs and HECATE Proteins Fine-Tunes Photomorphogenesis in Arabidopsis.

作者信息

Zhu Ling, Xin Ruijiao, Bu Qingyun, Shen Hui, Dang Jonathan, Huq Enamul

机构信息

Department of Molecular Biosciences and The Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas 78712.

Department of Molecular Biosciences and The Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas 78712

出版信息

Plant Cell. 2016 Apr;28(4):855-74. doi: 10.1105/tpc.16.00122. Epub 2016 Apr 12.

Abstract

The phytochrome interacting factors (PIFs), a small group of basic helix-loop-helix transcription factors, repress photomorphogenesis both in the dark and light. Light signals perceived by the phytochrome family of photoreceptors induce rapid degradation of PIFs to promote photomorphogenesis. Here, we show that HECATE (HEC) proteins, another small group of HLH proteins, antagonistically regulate PIFs to promote photomorphogenesis. HEC1 and HEC2 heterodimerize with PIF family members. PIF1, HEC1, and HEC2 genes are spatially and temporally coexpressed, and HEC2 is localized in the nucleus. hec1, hec2, and hec3 single mutants and the hec1 hec2 double mutant showed hyposensitivity to light-induced seed germination and accumulation of chlorophyll and carotenoids, hallmark processes oppositely regulated by PIF1. HEC2 inhibits PIF1 target gene expression by directly heterodimerizing with PIF1 and preventing DNA binding and transcriptional activation activity of PIF1. Conversely, PIFs directly activate the expression of HEC1 and HEC2 in the dark, and light reduces the expression of these HECs possibly by degrading PIFs. HEC2 is partially degraded in the dark through the ubiquitin/26S-proteasome pathway and is stabilized by light. HEC2 overexpression also reduces the light-induced degradation of PIF1. Taken together, these data suggest that PIFs and HECs constitute a negative feedback loop to fine-tune photomorphogenesis in Arabidopsis thaliana.

摘要

光敏色素互作因子(PIFs)是一小类碱性螺旋-环-螺旋转录因子,在黑暗和光照条件下均抑制光形态建成。光感受器光敏色素家族感知的光信号会诱导PIFs快速降解,以促进光形态建成。在此,我们表明,另一小类HLH蛋白HECATE(HEC)蛋白通过拮抗调控PIFs来促进光形态建成。HEC1和HEC2与PIF家族成员形成异源二聚体。PIF1、HEC1和HEC2基因在空间和时间上共表达,且HEC2定位于细胞核。hec1、hec2和hec3单突变体以及hec1 hec2双突变体对光诱导的种子萌发以及叶绿素和类胡萝卜素积累表现出低敏感性,而这些标志性过程受PIF1的反向调控。HEC2通过与PIF1直接形成异源二聚体,并阻止PIF1的DNA结合和转录激活活性,从而抑制PIF1靶基因的表达。相反,PIFs在黑暗中直接激活HEC1和HEC2的表达,而光照可能通过降解PIFs来降低这些HEC的表达。HEC2在黑暗中通过泛素/26S蛋白酶体途径部分降解,并在光照下稳定。HEC2过表达也会减少光诱导的PIF1降解。综上所述,这些数据表明PIFs和HECs构成一个负反馈环,以微调拟南芥中的光形态建成。

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