scholarly journals Iron and Phosphate Deficiency Regulators Concertedly Control Coumarin Profiles in Arabidopsis thaliana Roots During Iron, Phosphate, and Combined Deficiencies

2019 ◽  
Vol 10 ◽  
Author(s):  
Ranju Chutia ◽  
Steffen Abel ◽  
Jörg Ziegler
Plant Biology ◽  
2020 ◽  
Vol 22 (5) ◽  
pp. 753-760 ◽  
Author(s):  
X. Lu ◽  
X. Li ◽  
D. Xie ◽  
C. Jiang ◽  
C. Wang ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e75452 ◽  
Author(s):  
Natasha Savage ◽  
Thomas J. W. Yang ◽  
Chung Ying Chen ◽  
Kai-Lan Lin ◽  
Nicholas A. M. Monk ◽  
...  

Author(s):  
Huiling Gao ◽  
Tian Wang ◽  
Yanting Zhang ◽  
Lili Li ◽  
Chuanqing Wang ◽  
...  

2019 ◽  
Author(s):  
Fangwei Yu ◽  
Shenyun Wang ◽  
Wei Zhang ◽  
Hong Wang ◽  
Li Yu ◽  
...  

Abstract Background The MYB transcription factor (MYB TF) family has been reported to be involved in the regulation of biotic and abiotic stresses in plants. However, the involvement of MYB TF in phosphate remobilization under phosphate deficiency remains largely unexplored. Results Here, we showed that an R2R3 type MYB transcription factor, MYB103, was involved in the tolerance to P deficiency in Arabidopsis thaliana . AtMYB103 was induced by P deficiency, and loss function of AtMYB103 significantly enhanced sensitivity to P deficiency, as root and shoot biomass and soluble P content in the myb103 mutant were significantly lower than those in wild-type (WT) plants under the P-deficient condition. Furthermore, the expression of Pi deficiency -responsive genes was more profound in myb103 than in WT. In addition, AtMYB103 may also be involved in the cell wall-based P reutilization, as less P was released from the cell wall in myb103 than in WT, which was in company with a reduction of the ethylene production. Conclusions These findings uncover the role of MYB103 in the P remobilization, presumably through ethylene signaling.


2020 ◽  
Vol 253 ◽  
pp. 153266
Author(s):  
Huiling Gao ◽  
Chuanqing Wang ◽  
Lili Li ◽  
Dali Fu ◽  
Yanting Zhang ◽  
...  

2000 ◽  
Vol 28 (6) ◽  
pp. 729-732 ◽  
Author(s):  
H. Härtel ◽  
C. Benning

To explore the role of digalactosyldiacylglycerol (DGDG) in plants the dgd1 mutant of Arabidopsis thaliana was grown in the presence and absence of inorganic phosphate. Phosphate deficiency in the dgd1 mutant causes a strong decrease in all phospholipids accompanied by an increase in DGDG and sulpholipid. Moreover, a significant DGDG accumulation was found in roots upon phosphate deprivation as well. Our data indicate that DGDG accumulation upon phosphate deprivation is due to the activation of a specific eukaryotic dgd1-independent biosynthetic pathway. We propose that DGDG may substitute for phosphatidylcholine upon phosphate deprivation.


2020 ◽  
Author(s):  
Ghazanfar Abbas Khan ◽  
Jules Deforges ◽  
Rodrigo S. Reis ◽  
Yi-Fang Hsieh ◽  
Jonatan Montpetit ◽  
...  

AbstractTranscription termination has important regulatory functions, impacting mRNA stability, localization and translation potential. Failure to appropriately terminate transcription can also lead to read-through transcription and the synthesis of antisense RNAs which can have profound impact on gene expression. The Transcription-Export (THO/TREX) protein complex plays an important role in coupling transcription with splicing and export of mRNA. However, little is known about the role of the THO/TREX complex in the control of transcription termination. In this work, we show that two proteins of the THO/TREX complex, namely TREX COMPONENT 1 (TEX1 or THO3) and HYPER RECOMBINATION1 (HPR1 or THO1) contribute to the correct transcription termination at several loci in Arabidopsis thaliana. We first demonstrate this by showing defective termination in tex1 and hpr1 mutants at the nopaline synthase (NOS) terminator present in a T-DNA inserted between exon 1 and 3 of the PHO1 locus in the pho1-7 mutant. Read-through transcription beyond the NOS terminator and splicing-out of the T-DNA resulted in the generation of a near full-length PHO1 mRNA (minus exon 2) in the tex1 pho1-7 and hpr1 pho1-7 double mutants, with enhanced production of a truncated PHO1 protein that retained phosphate export activity. Consequently, the strong reduction of shoot growth associated with the severe phosphate deficiency of the pho1-7 mutant was alleviated in the tex1 pho1-7 and hpr1 pho1-7 double mutants. Additionally, we show that RNA termination defects in tex1 and hpr1 mutants leads to 3’UTR extensions in several plant genes. These results demonstrate that THO/TREX complex contributes to the regulation of transcription termination.Author summaryProduction of messenger RNAs (mRNAs) involves numerous steps including initiation of transcription, elongation, splicing, termination, as well as export out of the nucleus. All these steps are highly coordinated and failure in any steps has a profound impact on the level and identity of mRNAs produced. The THO/TREX protein complex is associated with nascent RNAs and contributes to several mRNA biogenesis steps, including splicing and export. However, the contribution of the THO/TREX complex to mRNA termination was poorly defined. We have identified a role for two components of the THO/TREX complex, namely the proteins TEX1 and HPR1, in the control of transcription termination in the plant Arabidopsis thaliana. We show that the tex1 and hpr1 mutants have defects in terminating mRNA at the nopaline synthase (NOS) terminator found in T-DNA insertion mutants leading to the transcriptional read-through pass the NOS terminator. We also show that tex1 and hpr1 mutants have defects in mRNA termination at several endogenous genes, leading to the production of 3’UTR extensions. Together, these results highlight a role for the THO/TREX complex in mRNA termination.


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