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小麦 bHLH 结构域蛋白基因的分离与鉴定及其对叶绿素合成的负调控

Isolation and Identification of a Wheat Gene Encoding a bHLH Domain Protein, Which Negatively Regulates Chlorophyll Biosynthesis in .

机构信息

Key Laboratory of Crop Heterosis of Shaanxi Province, Wheat Breeding Engineering Research Center, Ministry of Education, College of Agronomy, Northwest A & F University, Yangling 712100, Shaanxi, China.

College of Plant Protection, Northwest A & F University, Yangling 712100, Shaanxi, China.

出版信息

Int J Mol Sci. 2020 Jan 17;21(2):629. doi: 10.3390/ijms21020629.

Abstract

Chlorophyll biosynthesis plays a vital role in chloroplast development and photosynthesis in plants. In this study, we identified an orthologue of the rice gene ( L., Tapetum Degeneration Retardation) in wheat ( L.) called () by sequence comparison. TaTDRL encodes a putative 557 amino acid protein with a basic helix-loop-helix (bHLH) conserved domain at the C-terminal (295-344 aa). The TaTDRL protein localised to the nucleus and displayed transcriptional activation activity in a yeast hybrid system. was expressed in the leaf tissue and expression was induced by dark treatment. Here, we revealed the potential function of gene in wheat by utilizing transgenic plants TaTDRL overexpressing (TaTDRL-OE) and TaTDRL-EAR (EAR-motif, a repression domain of only 12 amino acids). Compared with wild-type plants (WT), both TaTDRL-OE and TaTDRL-EAR were characterized by a deficiency of chlorophyll. Moreover, the expression level of the chlorophyll-related gene () in TaTDRL-OE and TaTDRL-EAR was lower than that of WT. We found that TaTDRL physically interacts with wheat Phytochrome Interacting Factor 1 (PIF1) and Arabadopsis PIF1, suggesting that TaTDRL regulates light signaling during dark or light treatment. In summary, TaTDRL may respond to dark or light treatment and negatively regulate chlorophyll biosynthesis by interacting with AtPIF1 in transgenic .

摘要

叶绿素生物合成在植物叶绿体发育和光合作用中起着至关重要的作用。在这项研究中,我们通过序列比较,在小麦(L.)中鉴定到一个与水稻基因(L.,花粉退化延迟)的同源物,称为()。TaTDRL 编码一个假定的 557 个氨基酸的蛋白质,在 C 端(295-344 aa)具有一个基本螺旋-环-螺旋(bHLH)保守结构域。TaTDRL 蛋白定位于细胞核,并在酵母杂交系统中显示转录激活活性。在叶片组织中表达,黑暗处理可诱导表达。在这里,我们通过利用转基因(TaTDRL-OE 和 TaTDRL-EAR)过表达和 TaTDRL-EAR(EAR 基序,仅 12 个氨基酸的抑制域)的小麦()揭示了该基因在小麦中的潜在功能。与野生型植物(WT)相比,TaTDRL-OE 和 TaTDRL-EAR 都表现出叶绿素缺乏的特征。此外,TaTDRL-OE 和 TaTDRL-EAR 中叶绿素相关基因()的表达水平低于 WT。我们发现 TaTDRL 与小麦光受体相互作用因子 1(PIF1)和拟南芥 PIF1 发生物理相互作用,表明 TaTDRL 在黑暗或光照处理期间调节光信号。总之,TaTDRL 可能通过与 AtPIF1 相互作用,对黑暗或光照处理做出反应,并负调控转基因小麦中的叶绿素生物合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d67f/7014150/e87409d9bb13/ijms-21-00629-g001.jpg

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