2020
DOI: 10.1093/jxb/eraa355
|View full text |Cite
|
Sign up to set email alerts
|

The MYB transcription factor TaPHR3-A1 is involved in phosphate signaling and governs yield-related traits in bread wheat

Abstract: Improved inorganic phosphate (Pi) use efficiency in crops will be important for sustainable agriculture. Exploring molecular mechanisms that regulate Pi uptake could provide useful information for breeding wheat with improved Pi use efficiency. Here, a TaPHR3-A1 (Gene ID: TraesCS7A02G415800), ortholog of rice OsPHR3 that functions in transcriptional regulation of Pi signaling, was cloned from wheat chromosome 7A. Ectopic expression of TaPHR3-A1 in Arabidopsis and rice gave in enhanced vegetative growth and mor… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
7
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
9

Relationship

3
6

Authors

Journals

citations
Cited by 20 publications
(11 citation statements)
references
References 71 publications
1
7
0
Order By: Relevance
“…Phytohormone signallings of LR and AR formation have been evidenced to be subject to the regulatory mechanisms in which TFs are the major players (Bellini et al ., 2014 ; Crombez et al ., 2019 ). Among Pi starvation‐related TFs, PHOSPHATE RESPONSE 1 (PHR1), a MYB coiled‐coil domain TF (Dubos et al ., 2010 ; Sega and Pacak, 2019 ), is known as the master regulator that mediates phosphate starvation response in Arabidopsis (Devaiah et al ., 2009 ), bread wheat (Zheng et al ., 2020 ), rice (Dai et al ., 2012 ; Rubio et al ., 2001 ), and soybean (Xue et al ., 2017 ); thousands of phytohormone signalling factors and many other LR‐related TFs have been identified to be the direct targets of PHR1 (Castrillo et al ., 2017 ). PHR1 and related TFs have been suggested to be the major players in Pi‐starvation‐induced LR formation (Crombez et al ., 2019 ).…”
Section: Introductionmentioning
confidence: 99%
“…Phytohormone signallings of LR and AR formation have been evidenced to be subject to the regulatory mechanisms in which TFs are the major players (Bellini et al ., 2014 ; Crombez et al ., 2019 ). Among Pi starvation‐related TFs, PHOSPHATE RESPONSE 1 (PHR1), a MYB coiled‐coil domain TF (Dubos et al ., 2010 ; Sega and Pacak, 2019 ), is known as the master regulator that mediates phosphate starvation response in Arabidopsis (Devaiah et al ., 2009 ), bread wheat (Zheng et al ., 2020 ), rice (Dai et al ., 2012 ; Rubio et al ., 2001 ), and soybean (Xue et al ., 2017 ); thousands of phytohormone signalling factors and many other LR‐related TFs have been identified to be the direct targets of PHR1 (Castrillo et al ., 2017 ). PHR1 and related TFs have been suggested to be the major players in Pi‐starvation‐induced LR formation (Crombez et al ., 2019 ).…”
Section: Introductionmentioning
confidence: 99%
“…Other grain-related QTL in cereals overlapped marker Xbarc121, a flanking marker of QHtscc.ksu-7A. Several QTL controlling thousand-grain weight and grain number in bread wheat for grain weight per plant in durum wheat, panicle number, seed setting rate, and grain weight per plant in rice also overlapped Xbarc121 and therefore QHtscc.ksu-7A [35,36].…”
Section: Targeted Genomic Regions Of Nils Overlap Previously Reported Qtl For Root Traits and Other Yield-related Traitsmentioning
confidence: 92%
“…MYB transcription factor (TF) encoding genes in wheat, such as TaPHR3-A1 and TaSIM, improved P uptake, salt stress tolerance, grain number, and notably root length in Arabidopsis [35,50]. A mutant of soybean overexpressing wheat R2R3-MYB TF (GmMYB84) had greater primary rooting depth at optimum reactive oxygen species (ROS) level and drought tolerance [51].…”
Section: Putative Candidate Genes Controlling Wheat Root Traitsmentioning
confidence: 99%
“…Quantitative real-time PCR was performed using SYBR® Premix Ex Taq™ II (Takara) according to the manufacturer’s instructions on a 7,300 Real-time PCR System (Applied Biosystems), where the relative expression of each gene was calculated according to the 2 −ΔΔCT method ( Zheng et al, 2020 ). The glyceraldehyde-3-phosphate dehydrogenase gene was used as an endogenous reference for real-time PCR, and all analyses were performed with three technical and three biological replications.…”
Section: Methodsmentioning
confidence: 99%