Identification of Novel Genes in Arabidopsis Involved in Secondary Cell Wall Formation Using Expression Profiling and Reverse Genetics

By David M Brown, L. Zeef, Joanne Ellis, Royston Goodacre, S. Turner. The Plant Cell Online, 2005

822 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/3b5f3b5edc1119fed402160192af762e7cd1cc55

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Citations in the corpus

The NAC Transcription Factors NST1 and NST2 of Arabidopsis Regulate Secondary Wall Thickenings and Are Required for Anther Dehiscencew⃞ (2005, background): “…IRX4, and IRX12 genes encode a cellulose synthase that is specific for secondary walls (Taylor et al., 1999), cinnamoyl-CoA reductase, which is involved in lignin biosynthesis (Jones et al., 2001), and a putative laccase that is involved in lignin biosynthesis (Brown et al., 2005), respectively.”
SND1, a NAC Domain Transcription Factor, Is a Key Regulator of Secondary Wall Synthesis in Fibers of Arabidopsis[W] (2006, background): “In addition, genomic analysis revealed a number of novel glycosyltransferases that might be involved in secondary wall synthesis (Aspeborg et al., 2005; Brown et al., 2005; Persson et al., 2005).”
Quantitative trait locus (QTL) analysis of wood quality traits in Eucalyptus nitens (2010, background): “COBL4 has been shown to be involved in cellulose synthesis in a number of species (Brown et al. 2005; Ching et al. 2006; Li et al. 2003).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “The concept of KNAT7 functioning as a negative regulator of secondary cell wall deposition is consistent with the thinner secondary cell wall phenotypes observed in Arabidopsis fibres in response to either KNAT7 overexpression or overexpression of KNAT7 dominant repression constructs designed to rep”
The cell biology of lignification in higher plants. (2015, background): “However, this cell specificity for phenoloxidases is not so clear-cut as xylem TE lignification requires both laccases and peroxidases (Table 5), and collapsed TE phenotypes have been observed in lossof-function mutants of both At-LAC4 (Brown et al., 2005; Berthet et al., 2011) and At-PRX72 (Herrero”
NAC Transcription Factors, NST1 and NST3, Are Key Regulators of the Formation of Secondary Walls in Woody Tissues of Arabidopsis[W][OA] (2007, methodology): “IRX3 and IRX5 encode cellulose synthase (Taylor et al., 1999, 2003), IRX4, IRX12, and At OMT1 are related to lignin biosynthesis (Muzac et al., 2000; Jones et al., 2001; Brown et al., 2005; Sawa et al., 2005), and FRA8 is considered to function in the biosynthesis of xylan (Zhong et al., 2005).”
Lignin Biosynthesis and Structure1 (2010, background): “This “irregular xylem” phenotype, indicative of reduced mechanical cell wall strength, is not unique to reductions in lignin, as it is also noted in mutants with defects in the biosynthesis of other cell wall polymers (Brown et al., 2005).”
An Arabidopsis Gene Regulatory Network for Secondary Cell Wall Synthesis (2014, methodology): “The analysis performed was categorized as (1) supervised tier Ia, network inferred with SIRENE with the provided”
Plant cell walls: the skeleton of the plant world (2010, methodology): “The IRX and PARVUS genes and their homologues in poplar and rice were all initially identified by correlative expression analyses using EST ormicroarray data aimed at identifying genes that function in secondary wall polysaccharide synthesis, including xylan (Aspeborg et al. 2005; Brown et al. 2005;”