Class II KNOX Transcription Factors

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This entry is adapted from the peer-reviewed paper 10.3390/plants11040493

Knotted-like homeobox (KNOX) genes encode homeodomain-containing transcription factors (TFs) that modulate various important developmental processes in plants. While Class I KNOX TF genes are mainly expressed in the shoot apical meristems of both monocot and eudicot plants and are involved in meristem maintenance and/or formation, Class II KNOXTF genes exhibit diverse expression patterns and their precise functions have mostly remained unknown. The expression patterns of Class II KNOX TF genes in Arabidopsis, namely KNAT3, KNAT4, KNAT5, and KNAT7, suggest that TFs encoded by at least some of these genes, such as KNAT7 and KNAT3, may play a significant role in secondary cell wall formation.

bioethanol KNOX II transcription factors saccharification secondary cell walls xylan xylem and fiber development

1. KNOX Genes and Encoded KNOX Proteins in Plants

The KNOX genes are members of one of the ancestral gene families involved in the transition of plants from an aquatic to a terrestrial habitat during evolution ^[1]. KNOX genes encode homeodomain (HD)-containing TFs involved in various developmental processes. Typical HD proteins contain 60 amino acids, while the HD of KNOX proteins contains a highly conserved 63-amino acid stretch consisting of three ∝-helices that form a helix-turn-helix-type DNA binding motif ^[2] (Figure 1). Due to the presence of three extra amino acids between the first and second helices, all KNOX TF proteins are included in the TALE (three amino acid loop extension) superclass, the members of which are evolutionarily conserved from single-cell algae to higher plants ^[3]. The sequence immediately upstream of the HD, the ELK domain, has been suggested to function as a nuclear localization signal and be involved in protein–protein interactions ^[3]. In addition to the HD and ELK domains, a stretch of 100 amino acids located at the N terminus of almost all KNOX proteins, the MEINOX domain, also functions in protein–protein interactions ^[3]. This MEINOX domain in plants consists of two smaller domains, KNOX1 and KNOX2, separated by a poorly conserved linker sequence (Figure 1).

Figure 1. KNOX protein domain organization comprising MEINOX, ELK, and the TALE homeodomain (HD). The TALE homeodomain consists of three α-helices which comprise a helix-turn-helix type DNA binding motif, and contains three extra residues (PYP) in the loop between the first and second helices as compared to typical HDs. The MEINOX domain is present at the N terminus of the KNOX proteins, and it functions during protein–protein interactions. This MEINOX domain in plants is made of two smaller domains, KNOX1 and KNOX2, separated by a linker sequence. The ELK domain has been suggested to function as a nuclear localization signal and be involved in protein–protein interactions. The relatively small and less well-conserved amino acid motif located between the MEINOX and ELK domains is called the GSE domain; its function is not well understood.

Plant KNOX genes are divided into three subclasses based on their sequence similarity within the HD encoding regions, intron positions, expression patterns, and phylogenetic analysis ^[4]^[5]^[6]^[7]. Class I KNOX genes are similar to the knotted1 gene of maize ^[8] and are mainly expressed in the shoot apical meristems (SAMs) of both monocot and eudicot plants. The Class I KNOX genes STM, KNAT1/BP, KNAT2, and KNAT6 in Arabidopsis play an important role in the transcriptional regulation of meristem development, leaf shape control, and hormone homeostasis ^[9]. Loss-of-function mutations in these genes affect meristem maintenance and/or formation ^[10]. The only member of Class III KNOX gene, KNATM, is involved in the regulation of leaf polarity, leaf shape, and compound leaf development ^[11]. Four Class II KNOX genes (KNAT3, KNAT4, KNAT5, and KNAT7) in Arabidopsis form a separate monophyletic group and have several orthologues in higher plant genomes with few known functions ^[6]^[7]^[12]. Interestingly, Class II KNOX genes have been suggested to regulate the haploid-to-diploid morphological transition in land plants ^[1]. The first plant homeobox gene was discovered over 25 years ago; however, researchers only recently began to decipher the roles of Class II KNOX genes in higher plant growth and development. This entry focuses on the functions of Class II KNOX genes and their encoded proteins in higher plants.

2. The Expression Patterns of Class II KNOX Genes in Plants Provide Some Clues about Their Functionality in SCW Formation

The only Class II KNOX gene that has recently been well characterized and extensively studied is KNAT7 ^[13]^[14]^[15]^[16]^[17]^[18]^[19]. The role of KNAT7 TF as a regulator in SCW biosynthesis was first reported in Arabidopsis through the observation of the irx (irregular xylem) phenotype that occurred in a loss-of-function knat7 mutant, irx11 ^[18]. At the same time, the tight co-expression of the KNAT7 TF gene along with SCW-specific CesA genes was reported using microarrays of Arabidopsis inflorescence stems undergoing SCW formation ^[20]^[21]. Promoter-GUS expression studies of AtKNAT7 in Arabidopsis showed that it is highly expressed in developing xylem, phloem fibers, and cambium cells of inflorescence stems ^[14]. Wang et al. ^[16] recently examined whether several Class II KNOX genes from Arabidopsis, KNAT3, KNAT4, KNAT5, and KNAT7, were expressed during SCW deposition. All these Class II KNOX gene promoters regulated GUS expression in the vascular bundles in younger stems and intrafascicular fibers and vessel cells in older stems. These observations suggest that these Class II KNOX genes have similar expression patterns during the deposition of the SCWs. Qin et al. ^[17] also showed that while KNAT7 expression was much higher in stem tissues, KNAT3 expression remained similar in all tissues examined. Promoter-GUS fusions confirmed that KNAT3 and KNAT7 genes are co-expressed in developing xylem and interfascicular fibers in the Arabidopsis stem.

In poplar (Populus balsamifera), the expression of PtKNAT7 gradually increases from the primary cell wall expansion stage to the mature xylem tissue formation stage, and from the youngest to the older internodes of stem ^[14]. Cotton GhKNL1 was reported to be preferentially expressed in developing cotton fibers during SCW biosynthesis ^[22]. Switchgrass KNAT7 also appears to be a functional ortholog of Arabidopsis KNAT7, based on its expression patterns ^[23]. In researchers' laboratory, researchers studied the expression patterns of two Class II KNOX genes, KNAT3 and KNAT7, in tobacco (Nicotiana benthamiana) ^[15]. Higher expression of NbKNAT7 was seen in older stems of tobacco showing secondary growth followed by young stems and old leaves, while NbKNAT3 displayed higher expression in older leaves followed by roots and young leaves. These two Class II KNOX genes were also found to be highly expressed during tension wood formation in aspen. The expression of NbKNAT3 and NbKNAT7 in young and old stems indicates that they play a role in wood formation. Thus, Class II KNOX genes are associated with SCW formation during xylem and fiber development.

3. Genetic Mutations in Class II KNOX Genes Further Clarify Their Role in SCW Formation

Until 2005, KNAT7 was not often discussed in mutation studies of the Class II KNOX genes; however, a number of Class II KNOX mutations have recently been studied in detail (Table 1). A T-DNA insertion in the intron of the KNAT7 gene resulted in a loss-of-function mutant, irx11, that showed only a moderately weak growth phenotype. The irx11 mutant also exhibited the typical irx phenotype in xylem vessels that were collapsed due to weak SCW formation. The irx11 mutant did not have significantly altered cellulose or xylan content compared to controls. No lignin content of these mutants was reported at that time. While discovering a set of novel TFs involved in SCW biosynthesis, Zhong et al. ^[13] associated KNAT7 expression with SCW formation, and the dominant repression of KNAT7 (DR-KNAT7 mutants) affected SCW formation in both xylem and fiber cells (Table 1). Curiously, they did not observe the typical irx phenomenon in these DR-KNAT7 mutants, a tell-tale sign of weak SCW formation; however, the cell wall thicknesses of both xylem vessels and fibers were reduced compared to controls (28% down in interfascicular fibers (IF), 26% down in vessels (V), and 80% down in xylary fibers (XF)). Several monosaccharides from the cell walls of DR-KNAT7 mutants were reduced by 20–30%, except for arabinose, which was increased by 18%. The overexpression of KNAT7 did not increase the SCW thickness of fibers and vessels. These results indicated that KNAT7 could be a positive regulator of SCW formation in Arabidopsis. However, Li et al. ^[14] reported a contrasting observation that loss-of-function mutants in the AtKNAT7 gene resulted in differential thicknesses of interfascicular and xylary fibers compared to vessels (58% up in IF, 35% down in V, and 31% up in XF; Table 1). The vessels walls were thinner, resulting in collapsed xylem vessels that showed the irx phenotype (similar to ^[18]); however, the interfascicular fibers were significantly thicker than in the wild type control, suggesting that KNAT7 is a transcriptional repressor of fiber SCW formation (but a transcriptional activator of vessel SCW formation). KNAT7 overexpression lines exhibited thinner fiber walls (57% down in IF) with normal vessel and xylary fiber cell walls. Interestingly, even though many SCW-specific cellulose and xylan synthesis genes were upregulated in these mutants, no quantitative changes in cellulose or xylan were reported. All ten lignin synthesis genes tested were upregulated along with an 11% increase in lignin content of cell walls from the stem. Li et al. ^[18] speculated that KNAT7 interacts with different partner proteins in different cell types to form functionally distinct complexes. Recently, the regulatory roles of other members of the Class II KNOX gene family, KNAT3, KNAT4, and KNAT5, in SCW formation were explored in Arabidopsis inflorescence stems ^[16]^[17] (Table 1). Loss-of-function mutants of knat3, knat4, and knat5 did not produce any irx phenotype, as observed in the case of loss-of-function mutants of knat7 ^[16]. This could be due to the functional redundancy of KNOX II genes. However, knat3/knat7 double mutants displayed an enhanced irx phenotype compared to single knat7 mutants. These double mutants had thinner interfascicular fiber cell walls compared to the single mutants and wild-type plants (40% down in IF) indicating a potentially positive regulatory role of KNAT3 in combination with KNAT7 in xylem SCW development. Even though many SCW genes were highly expressed in the knat3/knat7 double mutants, the cellulose and xylan contents of their cell walls were reduced by 19% and 43%, respectively, and the changes in lignin content were not significant. The Syringyl to Guaicyl (S/G) lignin ratio was down by 83%; however, it was not possible to correlate all these cell wall content changes with the changes in gene expression patterns. In addition, the severe irx phenotype in these double mutants indicated the overlapping roles and partial functional redundancy of KNAT3 and KNAT7 in xylem vessel development during SCW formation. Furthermore, KNAT3 overexpression in Arabidopsis resulted in thickened interfascicular fibers in the SCW of inflorescence stems ^[16]. This entry described KNAT3 as a potential transcriptional activator, working together with KNAT7 to promote SCW biosynthesis in xylem vessels. A synergistic interaction of KNAT3 and KNAT7 to regulate monolignol biosynthesis in Arabidopsis was also reported in another study ^[17]. Most importantly, they attempted to link S-lignin formation with KNAT3 and KNAT7 expression; however, they could not show the direct transcriptional regulation of a key gene, ferulate 5-hydroxylase (F5H), involved in S-lignin formation by KNAT3 or KNAT7. Similar to the earlier observation by Wang et al. ^[16], the overexpression of KNAT3 also caused thickening in the interfascicular fiber walls, indicating the positive regulation of interfascicular fiber wall development by KNAT3. These studies by Wang et al. and Qin et al. ^[16]^[17] reconciled the paradoxical observations about KNAT7 mutants in Arabidopsis and indicated that KNAT3 and KNAT7 might be working synergistically in fibers, but antagonistically in vessels, during the regulation of SCW biosynthesis (Table 1).

Table 1. Gene Mutations in Class II KNOX genes and their effect on SCW formation.

Target Gene	Mutation	Type of Mutation	Anatomy of Mutants	References
AtKNAT7	irx11	T-DNA insertion	Irregular xylem with collapsed vessels.	^[18]
AtKNAT7	-	Dominant repression	Reduced cell wall thickness of both xylem vessels and fibers; reduced composition of several monosaccharides from the cell walls.	^[13]
AtKNAT7	irx11	Loss-of-function mutation	Thinner vessels walls resulted in a collapse of xylem vessels that showed the irx phenotype and thicker interfascicular fibers compared to controls; increase in lignin content.	^[14]
AtKNAT3, AtKNAT4, AtKNAT5	Single mutants	T-DNA insertion	No irx phenotype.	^[16]
KNAT3/KNAT7	Double mutant	T-DNA insertion	Enhanced irregular xylem (irx) phenotype characterized by weak inflorescence stem; reduced interfascicular fiber wall thickness and modified cell wall composition.	^[16]
KNAT3/KNAT7	Double mutant	Chimeric repression	Thinner interfascicular fiber cell walls compared to single mutants and wild type (WT); reduced cellulose and xylan and reduced S/G lignin ratio.	^[17]
OsKNAT7	CRISPR/CAS9	T-DNA insertion	Thicker fiber cell walls; larger grain size due to cell expansion in spikelet bracts.	^[24]
GhKNL1	-	Dominant repression	Abnormal shorter fiber length.	^[22]

4. Targeted Genetic Manipulations in Class II KNOX Genes Confirm Their Role in SCW Formation

Apart from the detailed study of Class II KNOX gene mutants, targeted genetic manipulations of Class II KNOX genes, especially, KNAT7 genes have offered some additional clues regarding the functions of these genes (Table 2). While the overexpression of KNAT7 in Arabidopsis did not produce any specific SCW phenotype ^[13], subsequently, Li et al. ^[14] reported that such experiments produced thin interfascicular fibers without any changes in wall thickness of vessels suggesting that KNAT7 TF is indeed a regulator of SCW formation.

Table 2. Genetic manipulation of Class II KNOX genes in different plant species.

Gene Used	Target Plant	Gene Modification Method	Impact on Transgenic Plants	References
AtKNAT7	Arabidopsis	Overexpression	Thin interfascicular fiber walls, but no change in vessel wall thickness.	^[14]
Cotton GhKNL1	Arabidopsis	Overexpression	Thinner interfascicular fibers and slightly thinner vessel walls, but no change in xylary fibers.	^[22]
Cotton GhKNAT7	Arabidopsis	Overexpression	Reduced deposition of lignocellulose in interfascicular fibers, but no change in the SCWs of xylem fibers and vessels.	^[7]
NbKNAT7	Tobacco	Downregulation by VIGS and RNAi	Increased xylem proliferation with thin-walled fiber cells, increased polysaccharide extractability, and higher saccharification rate.	^[15]
AtKNAT7	Arabidopsis	Dominant repression	Reduced expression of SCW genes that resulted in thinner fiber cell walls with altered cell wall composition.	^[13]
PtKNAT7	Poplar	Overexpression	Enhanced expression of SCW genes, CesA8, IRX9, PAL, and CCR.	^[25]
PtKNAT7	Poplar	Downregulation by antisense	Reduced expression of SCW genes, reduced lignin content, altered lignin composition (S/G ratio), and increased saccharification.	^[25]

The successful complementation of Arabidopsis knat7 mutants with the overexpression of the cotton GhKNL1 gene ^[22] and poplar PtKNAT7 ^[14] rescued the defective irx phenotype of the knat7 mutants, suggesting the functional conservation of KNAT7 genes among Arabidopsis, cotton, and poplar. The overexpression of cotton GhKNL1 in Arabidopsis resulted in thinner interfascicular fibers and slightly thinner vessels walls without any change in the xylary fibers compared to control plants ^[22]. The overexpression of cotton GhKNAT7 significantly reduced the deposition of lignocellulose in the interfascicular fibers of Arabidopsis ^[7]. However, the SCWs of the xylem fibers and vessels in the transgenic plants did not show any difference from the control plants. The dominant repression of the same cotton KNAT7 orthologue in Arabidopsis produced thinner interfascicular fibers, but thicker vessels and xylary fiber walls, suggesting that KNAT7 can act as a negative or positive regulator of SCW formation in different cell types.

In researchers' laboratory, researchers generated RNAi lines of tobacco (N. benthamiana) that exhibited reduced expression of KNAT7 ^[15]. NbKNAT7 downregulated through a transient virus-induced gene silencing (VIGS) system resulted in increased xylem proliferation with thin-walled fiber cells. The glycome analyses of the cell walls showed increased polysaccharide extractability in 1 M KOH extracts of the VIGS-NbKNAT7 lines, suggestive of SCW loosening. In addition, there were increased saccharification rates (40% higher than control) in stems of VIGS-NbKNAT7 lines, which indicated the alteration of cell wall composition in VIGS lines downregulated for the NbKNAT7 gene. Similar to the VIGS results, the stems of stable RNAi lines also showed increased xylem area in their stems as compared to control stems ^[15]. The cell walls of xylem fibers were thinner (over 50%) in the RNAi lines as compared to vector control lines. The stems of KNAT7 repression lines in tobacco showed reduced expression of SCW genes that resulted in thinner fiber cell walls with altered cell wall composition ^[15]. All these results suggested that KNAT7 TF might act as a positive regulator of SCW formation in tobacco.

In a recent study performed in researchers' laboratory by Ahlawat et al. ^[25], transgenic poplar plants overexpressing PtKNAT7 and AtKNAT7 genes showed enhanced expression of the SCW genes CesA8, IRX9, PAL, and CCR, and reduced expression of the same genes in the poplar PtKNAT7 antisense plants. These results further suggested a positive regulatory role of KNAT7 in SCW formation in poplars. In addition, the genetic suppression of KNAT7 in transgenic poplar stems reduced lignin content by about 6% and altered the lignin composition (S/G ratio) of poplar wood with increased saccharification ability (44–53% higher saccharification efficiency over control plants). Yoo et al. ^[26] also reported a negative correlation between lignin content and the saccharification efficiency of woody tissues and a positive correlation between the S/G ratio and the saccharification efficiency of SCW biomass. Therefore, a change in the S/G ratio and reduction in lignin content might be important for improving the saccharification efficiency of SCW biomass. All the studies reported so far in Arabidopsis and other higher plants suggest that KNAT7 acts differentially as a negative and positive regulator of SCW biosynthesis in different cell types of the same plant or in different plant species.

5. Transcriptional Network of the Class II KNOX Genes Involved in SCW Formation

A complex network of transcription factors regulates SCW biosynthesis in plants ^[27]^[28]^[29]^[30]^[31]^[32]. Among these, some Class II KNOX TFs also regulate SCW biogenesis. The major constituents of the SCW are cellulose, lignin, and hemicelluloses ^[33]. Cellulose is a polymer of glucose synthesized at the plasma membrane by the cellulose synthase (CesA) complex ^[34], while lignin is composed of guaiacyl (G), syringyl (S), and p-hydroxyphenyl (H) units that are synthesized through the phenylpropanoid pathway ^[35]. Xylan is the major hemicellulose component in the SCW and consists of a linear backbone of β-(1–4)-linked D-xylosyl (Xyl) residues and α-linked (OMe(methyl)) glucuronic acid (GlcA) side branches ^[36]. Many specific genes involved in cellulose, hemicellulose, and lignin biosynthesis pathways have previously been identified in plants (e.g., ^[36]^[37]^[38]) and it was anticipated that Class II KNOX TF proteins might directly regulate the expression of some of these genes. The first direct evidence of KNAT7-mediated regulation of xylan biosynthesis in the SCW was reported only recently by He et al. ^[19], who demonstrated that KNAT7 physically binds to the promoters of the xylan biosynthetic genes, IRREGULAR XYLEM 9 (IRX9), IRX10, IRX14L, and FRAGILE FIBER 8 (FRA8; Figure 2). Wang et al. ^[39] also reported the involvement of KNAT7 in xylan synthesis during mucilage production. While various cellulose and lignin biosynthesis genes have been shown to be differentially expressed in various knat7 mutants and during the ectopic expression of the KNAT7 gene in transgenic plants, the direct regulation of any of these SCW genes by KNAT7 TF has not yet been reported. In addition, no information is currently available on transcriptional regulation by the TFs encoded by the other three Class II KNOX genes, namely KNAT3, KNAT4, and KNAT5, or their orthologs in any other plant species.

Figure 2. Transcriptional regulation pathway of KNAT7 gene. SCW-associated upstream transcription factors (MYB61, SND1/NST1/NST2, VND1/VND7) and MYB46 directly bind the binding sites in the KNAT7 gene promoter to regulate the expression of the KNAT7 gene. KNAT7 positively regulates the expression of various xylan synthesis genes (IRX9/10 and IRX14L/FRA8). Interactions between KNAT7 and KNAT3 TFs might regulate F5H expression, and the interactions between KNAT7 and BLH6 negatively regulate the expression of the homeodomain-ZIP (HD-ZIP) TF gene Revoluta. All these interactions ultimately regulate SCW formation in higher plants. All genes are shown as rounded rectangles and proteins are indicated by rectangles.

References

Sakakibara, K.; Ando, S.; Yip, H.K.; Tamada, Y.; Hiwatashi, Y.; Murata, T.; Deguchi, H.; Hasebe, M.; Bowman, J.L. KNOX2 Genes Regulate the Haploid-to-Diploid Morphological Transition in Land Plants. Science 2013, 339, 1067–1070.
Desplan, C.; Theis, J.; O’Farrell, P.H. The Sequence Specificity of Homeodomain-DNA Interaction. Cell 1988, 54, 1081–1090.
Burglin, T.R. Analysis of TALE Superclass Homeobox Genes (MEIS, PBC, KNOX, Iroquois, TGIF) Reveals a Novel Domain Conserved between Plants and Animals. Nucleic Acids Res. 1997, 25, 4173–4180.
Kerstetter, R.; Vollbrecht, E.; Lowe, B.; Veit, B.; Yamaguchi, J.; Hake, S. Sequence Analysis and Expression Patterns Divide the Maize Knotted1-like Homeobox Genes into Two Classes. Plant Cell 1994, 6, 1877–1887.
Bharathan, G.; Janssen, B.J.; Kellogg, E.A.; Sinha, N. Phylogenetic Relationships and Evolution of the KNOTTED Class of Plant Homeodomain Proteins. Mol. Biol. Evol. 1999, 16, 553–563.
Xiong, H.; Shi, A.; Wu, D.; Weng, Y.; Qin, J.; Ravelombola, W.S.; Shu, X.; Zhou, W. Genome-Wide Identification, Classification and Evolutionary Expansion of KNOX Gene Family in Rice (Oryza Sativa) and Populus (Populustrichocarpa). Am. J. Plant Sci. 2018, 9, 1071–1092.
Ma, Q.; Wang, N.; Hao, P.; Sun, H.; Wang, C.; Ma, L.; Wang, H.; Zhang, X.; Wei, H.; Yu, S. Genome-Wide Identification and Characterization of TALE Superfamily Genes in Cotton Reveals Their Functions in Regulating Secondary Cell Wall Biosynthesis. BMC Plant Biol. 2019, 19, 432.
Vollbrecht, E.; Veit, B.; Sinha, N.; Hake, S. The Developmental Gene Knotted-1 Is a Member of a Maize Homeobox Gene Family. Nature 1991, 350, 241–243.
Hake, S.; Smith, H.M.S.; Holtan, H.; Magnani, E.; Mele, G.; Ramirez, J. The Role of Knox Genes in Plant Development. Annu. Rev. Cell Dev. Biol. 2004, 20, 125–151.
Sakamoto, T.; Sato, Y.; Matsuoka, M. Function of KNOX Homeodomain Proteins in Plant Development. Plant Biotechnol. 2001, 18, 85–92.
Kimura, S.; Koenig, D.; Kang, J.; Yoong, F.Y.; Sinha, N. Natural Variation in Leaf Morphology Results from Mutation of a Novel KNOX Gene. Curr. Biol. 2008, 18, 672–677.
Di Giacomo, E.; Sestili, F.; Iannelli, M.A.; Testone, G.; Mariotti, D.; Frugis, G. Characterization of KNOX Genes in Medicago Truncatula. Plant Mol. Biol. 2008, 67, 135–150.
Zhong, R.; Lee, C.; Zhou, J.; McCarthy, R.L.; Ye, Z.-H. A Battery of Transcription Factors Involved in the Regulation of Secondary Cell Wall Biosynthesis in Arabidopsis. Plant Cell 2008, 20, 2763–2782.
Li, E.; Bhargava, A.; Qiang, W.; Friedmann, M.C.; Forneris, N.; Savidge, R.A.; Johnson, L.A.; Mansfield, S.D.; Ellis, B.E.; Douglas, C.J. The Class II KNOX Gene KNAT7 Negatively Regulates Secondary Wall Formation in Arabidopsis and Is Functionally Conserved in Populus. New Phytol. 2012, 194, 102–115.
Pandey, S.K.; Nookaraju, A.; Fujino, T.; Pattathil, S.; Joshi, C.P. Virus-Induced Gene Silencing (VIGS)-Mediated Functional Characterization of Two Genes Involved in Lignocellulosic Secondary Cell Wall Formation. Plant Cell Rep. 2016, 35, 2353–2367.
Wang, S.; Yamaguchi, M.; Grienenberger, E.; Martone, P.T.; Samuels, A.L.; Mansfield, S.D. The Class II KNOX Genes KNAT3 and KNAT7 Work Cooperatively to Influence Deposition of Secondary Cell Walls That Provide Mechanical Support to Arabidopsis Stems. Plant J. 2020, 101, 293–309.
Qin, W.; Yin, Q.; Chen, J.; Zhao, X.; Yue, F.; He, J.; Yang, L.; Liu, L.; Zeng, Q.; Lu, F.; et al. The Class II KNOX Transcription Factors KNAT3 and KNAT7 Synergistically Regulate Monolignol Biosynthesis in Arabidopsis. J. Exp. Bot. 2020, 71, 5469–5483.
Brown, D.M.; Zeef, L.A.H.; Ellis, J.; Goodacre, R.; Turner, S.R. Identification of Novel Genes in Arabidopsis Involved in Secondary Cell Wall Formation Using Expression Profiling and Reverse Genetics. Plant Cell 2005, 17, 2281–2295.
He, J.-B.; Zhao, X.-H.; Du, P.-Z.; Zeng, W.; Beahan, C.T.; Wang, Y.-Q.; Li, H.-L.; Bacic, A.; Wu, A.-M. KNAT7 Positively Regulates Xylan Biosynthesis by Directly Activating IRX9 Expression in Arabidopsis: KNAT7 Positively Regulates Xylan Biosynthesis. J. Integr. Plant Biol. 2018, 60, 514–528.
Ehlting, J.; Mattheus, N.; Aeschliman, D.S.; Li, E.; Hamberger, B.; Cullis, I.F.; Zhuang, J.; Kaneda, M.; Mansfield, S.D.; Samuels, L.; et al. Global Transcript Profiling of Primary Stems from Arabidopsis Thaliana Identifies Candidate Genes for Missing Links in Lignin Biosynthesis and Transcriptional Regulators of Fiber Differentiation: Global Transcript Profiling of Stems. Plant J. 2005, 42, 618–640.
Persson, S.; Wei, H.; Milne, J.; Page, G.P.; Somerville, C.R. Identification of Genes Required for Cellulose Synthesis by Regression Analysis of Public Microarray Data Sets. Proc. Natl. Acad. Sci. USA 2005, 102, 8633–8638.
Gong, S.-Y.; Huang, G.-Q.; Sun, X.; Qin, L.-X.; Li, Y.; Zhou, L.; Li, X.-B. Cotton KNL1, Encoding a Class II KNOX Transcription Factor, Is Involved in Regulation of Fibre Development. J. Exp. Bot. 2014, 65, 4133–4147.
Zhong, R.; Yuan, Y.; Spiekerman, J.J.; Guley, J.T.; Egbosiuba, J.C.; Ye, Z.-H. Functional Characterization of NAC and MYB Transcription Factors Involved in Regulation of Biomass Production in Switchgrass (Panicum Virgatum). PLoS ONE 2015, 10, e0134611.
Wang, S.; Yang, H.; Mei, J.; Liu, X.; Wen, Z.; Zhang, L.; Xu, Z.; Zhang, B.; Zhou, Y. Rice Homeobox Protein KNAT7 Integrates the Pathways Regulating Cell Expansion and Wall Stiffness. Plant Physiol. 2019, 181, 669–682.
Ahlawat, Y.K.; Nookaraju, A.; Harman-Ware, A.E.; Doeppke, C.; Biswal, A.K.; Joshi, C.P. Genetic Modification of KNAT7 Transcription Factor Expression Enhances Saccharification and Reduces Recalcitrance of Woody Biomass in Poplars. Front. Plant Sci. 2021, 12, 762067.
Yoo, C.G.; Dumitrache, A.; Muchero, W.; Natzke, J.; Akinosho, H.; Li, M.; Sykes, R.W.; Brown, S.D.; Davison, B.; Tuskan, G.A.; et al. Significance of Lignin S/G Ratio in Biomass Recalcitrance of Populus Trichocarpa Variants for Bioethanol Production. ACS Sustain. Chem. Eng. 2018, 6, 2162–2168.
Ko, J.-H.; Kim, W.-C.; Han, K.-H. Ectopic Expression of MYB46 Identifies Transcriptional Regulatory Genes Involved in Secondary Wall Biosynthesis in Arabidopsis. Plant J. 2009, 60, 649–665.
Zhong, R.; Ye, Z.-H. Complexity of the Transcriptional Network Controlling Secondary Wall Biosynthesis. Plant Sci. 2014, 229, 193–207.
Pimrote, K. Transcriptional Regulatory Network Controlling Secondary Cell Wall Biosynthesis and Biomass Production in Vascular Plants. Afr. J. Biotechnol. 2012, 11, 13928–13937.
Nakano, Y.; Yamaguchi, M.; Endo, H.; Rejab, N.A.; Ohtani, M. NAC-MYB-Based Transcriptional Regulation of Secondary Cell Wall Biosynthesis in Land Plants. Front. Plant Sci. 2015, 6.
Rao, X.; Dixon, R.A. Current Models for Transcriptional Regulation of Secondary Cell Wall Biosynthesis in Grasses. Front. Plant Sci. 2018, 9, 399.
Yu, Y. OsKNAT7 Bridges Secondary Cell Wall Formation and Cell Growth Regulation. Plant Physiol. 2019, 181, 385–386.
de Vries, L.; Guevara-Rozo, S.; Cho, M.; Liu, L.-Y.; Renneckar, S.; Mansfield, S.D. Tailoring Renewable Materials via Plant Biotechnology. Biotechnol. Biofuels 2021, 14, 167.
Joshi, C.P.; Bhandari, S.; Ranjan, P.; Kalluri, U.C.; Liang, X.; Fujino, T.; Samuga, A. Genomics of Cellulose Biosynthesis in Poplars. New Phytol. 2004, 164, 53–61.
Boerjan, W.; Ralph, J.; Baucher, M. Lignin Biosynthesis. Annu. Rev. Plant Biol. 2003, 54, 519–546.
Lee, C.; Teng, Q.; Zhong, R.; Ye, Z.-H. Molecular Dissection of Xylan Biosynthesis during Wood Formation in Poplar. Mol. Plant 2011, 4, 730–747.
Polko, J.K.; Kieber, J.J. The Regulation of Cellulose Biosynthesis in Plants. Plant Cell 2019, 31, 282–296.
Behr, M.; Guerriero, G.; Grima-Pettenati, J.; Baucher, M. A Molecular Blueprint of Lignin Repression. Trends Plant Sci. 2019, 24, 1052–1064.
Wang, Y.; Xu, Y.; Pei, S.; Lu, M.; Kong, Y.; Zhou, G.; Hu, R. KNAT7 Regulates Xylan Biosynthesis in Arabidopsis Seed-Coat Mucilage. J. Exp. Bot. 2020, 71, 4125–4139.

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Subjects: Plant Sciences

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YOGESH AHLAWAT

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Update Date: 24 Feb 2022

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