Evolutionary and comparative analysis of MYB and bHLH plant transcription factors.
By A. Feller, Katja Machemer, Edward L. Braun, Erich Grotewold. The Plant Journal, 2011
1,153 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/89505f9c0f7cd279b17ba3fc2bb7bafc4b445cc2
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
In Plant Science
- M. Tattini
- Ricardo H. Ramirez-Gonzalez
- P. Casati
- Cristobal Uauy
- Xiansheng Zhang
- Pengda Ma
- P. Borrill
- A. Osbourn
Citations in the corpus
- Flavonoids as antioxidants in plants: location and functional significance. (2012, background): “[92] A.”
- The Role of Stress-Responsive Transcription Factors in Modulating Abiotic Stress Tolerance in Plants (2020, background): “The family of bHLH transcription factors is widespread in eukaryotes, and has expanded in plants [78,79].”
- A Conserved Network of Transcriptional Activators and Repressors Regulates Anthocyanin Pigmentation in Eudicots[C][W][OPEN] (2014, background): “Although the origin of the MBW activator complex for anthocyanins has not been resolved, the occurrence of at least some common TF components in gymnosperms and angiosperms (Wilkins et al., 2009; Feller et al., 2011) indicates it preceded the development of colorful flowers and so likely arose initi”
- Flavonoids: biosynthesis, biological functions, and biotechnological applications (2012, background): “In addition, the evolution of MYB and bHLH plant families has been deeply analyzed from structural and functional perspectives (Feller et al., 2011).”
- expVIP: a Customizable RNA-seq Data Analysis and Visualization Platform1[OPEN] (2016, background): “Feller et al., 2011; Nakashima et al., 2012), but this joint analysis identi fi ed precise candidates in wheat based on available experimental data that can be further characterized.”
- Plant phenolics: recent advances on their biosynthesis, genetics, and ecophysiology. (2013, background): “Another group of repressor TFs of note is the LATERAL ORGAN BOUNDARY DOMAIN (LBD) family of three Znfinger TFs, which can suppress PAP1 production as part of the response to nitrogen status in A. thaliana [115].”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “In contrast, plant genomes are endowed with a larger array of bHLH transcription factors than the human genome (Feller et al., 2011) and some plant bHLH transcription factors interact with environment-regulated receptors (Leivar and Quail, 2011).”
- MYB Transcription Factors as Regulators of Phenylpropanoid Metabolism in Plants. (2015, background): “1R proteins participate in 26 morphogenesis, secondary metabolism, including phenylpropanoid-derived 27 compounds, circadian clock control, response to phosphate starvation, and flower and 28 fruit development (Feller et al., 2011).”
- The bHLH transcription factor MdbHLH3 promotes anthocyanin accumulation and fruit colouration in response to low temperature in apples. (2012, background): “However, the specific amino acids in the MIR of bHLH factors that are responsible for the interaction with MYB TFs have not yet been identified in anthocyanin-related bHLH regulators in plants (Feller et al. 2011).”