Walls are thin 1 (WAT1), an Arabidopsis homolog of Medicago truncatula NODULIN21, is a tonoplast-localized protein required for secondary wall formation in fibers

Ranocha, Philippe; Denancé, Nicolás; Vanholme, Ruben; Freydier, Amandine; Martinez, Yves; Hoffmann, Laurent; Köhler, L.; Pouzet, Cécile; Renou, Jean-Pierre; Sundberg, Björn; Boerjan, Wout; Goffner, Deborah

doi:10.1111/j.1365-313x.2010.04256.x

Cited by 170 publications

(217 citation statements)

References 62 publications

Supporting

Mentioning

207

Contrasting

Order By: Relevance

“…MtN3 and MtN21 also have recently been shown to be crucial for exine pattern formation and cell integrity of microspores (Guan et al, 2008) and secondary wall formation in xylary and cotton fibers (Ranocha et al, 2010), respectively. These genes code for transmembrane proteins involved in the cell wall development of specialized plant cells that require stringent impermeability to specific substances (e.g.…”

Section: Functional Differentiation Between M and Bs Cells And Identimentioning

confidence: 99%

Characterizing Regulatory and Functional Differentiation between Maize Mesophyll and Bundle Sheath Cells by Transcriptomic Analysis

et al. 2012

View full text Add to dashboard Cite

To study the regulatory and functional differentiation between the mesophyll (M) and bundle sheath (BS) cells of maize (Zea mays), we isolated large quantities of highly homogeneous M and BS cells from newly matured second leaves for transcriptome profiling by RNA sequencing. A total of 52,421 annotated genes with at least one read were found in the two transcriptomes. Defining a gene with more than one read per kilobase per million mapped reads as expressed, we identified 18,482 expressed genes; 14,972 were expressed in M cells, including 53 M-enriched transcription factor (TF) genes, whereas 17,269 were expressed in BS cells, including 214 BS-enriched TF genes. Interestingly, many TF gene families show a conspicuous BS preference in expression. Pathway analyses reveal differentiation between the two cell types in various functional categories, with the M cells playing more important roles in light reaction, protein synthesis and folding, tetrapyrrole synthesis, and RNA binding, while the BS cells specialize in transport, signaling, protein degradation and posttranslational modification, major carbon, hydrogen, and oxygen metabolism, cell division and organization, and development. Genes coding for several transporters involved in the shuttle of C 4 metabolites and BS cell wall development have been identified, to our knowledge, for the first time. This comprehensive data set will be useful for studying M/BS differentiation in regulation and function.C 4 plants, with few exceptions, require the coordination of the mesophyll (M) and bundle sheath (BS) cells, arranged in a wreath structure called Kranz leaf anatomy (Hatch and Agostino, 1992), to confer high rates of photosynthesis. The initial carboxylation phase of the C 4 pathway takes place in the M cells, while the decarboxylation phase is restricted to the BS cells. The high photosynthetic capacity of C 4 plants implies a massive efflux of C 4 -related metabolites between M and BS cells and between the cytosol and organelles in each cell type (Weber and von Caemmerer, 2010).Although research in the past few decades has greatly increased our understanding of the biochemical reactions and the enzymes involved in the C 4 pathway of photosynthesis, little is known about the specific genes involved in the development of the Kranz leaf anatomy, the C 4 biochemical pathway, and the underlying regulatory mechanisms for the high-level expression of C 4 -specific genes in a cell-, organ-, or development-specific manner. With the advancement in genomics, the genomic sequences of several C 3 and C 4 model plants have become available. These advances have allowed in-depth comparative proteomic and transcriptomic analyses of the whole leaves of typical C 3 and C 4 plants and their closely related C 3 -C 4 intermediate species of Cleome and Flaveria . These comparative studies allow deduction on how many genes are required to make a C 4 plant and possibly on how they may have been regulated at the genetic level. In addition, attempts have been made recently to characterize...

show abstract

Section: Functional Differentiation Between M and Bs Cells And Identimentioning

confidence: 99%

Characterizing Regulatory and Functional Differentiation between Maize Mesophyll and Bundle Sheath Cells by Transcriptomic Analysis

et al. 2012

View full text Add to dashboard Cite

show abstract

“…The MtN21 proteins group in six major subfamilies, which are separated by more than 50 changes each. WAT1 (Ranocha et al, 2010) is located in group V; SIAR1 is located in subgroup IIIa.…”

Section: Expression In Yeast and Oocytes Shows That Siar1 Mediates Bomentioning

confidence: 99%

“…SIAR1 (At1g44800) belongs to group IIIa and has two closely related paralogs in Arabidopsis that are encoded by At1g21890 and At4g08300, but there are no direct orthologs in rice. WAT1 (At1g75500), the first described member of the family (Ranocha et al, 2010), is a distant homolog of SIAR1 and belongs to group V in the phylogram.…”

Section: Structure and Subgroups Of The Mtn21 Protein Family In Arabimentioning

confidence: 99%

See 1 more Smart Citation

Siliques Are Red1 from Arabidopsis Acts as a Bidirectional Amino Acid Transporter That Is Crucial for the Amino Acid Homeostasis of Siliques

et al. 2012

View full text Add to dashboard Cite

Many membrane proteins are involved in the transport of nutrients in plants. While the import of amino acids into plant cells is, in principle, well understood, their export has been insufficiently described. Here, we present the identification and characterization of the membrane protein Siliques Are Red1 (SIAR1) from Arabidopsis (Arabidopsis thaliana) that is able to translocate amino acids bidirectionally into as well as out of the cell. Analyses in yeast and oocytes suggest a SIAR1-mediated export of amino acids. In Arabidopsis, SIAR1 localizes to the plasma membrane and is expressed in the vascular tissue, in the pericycle, in stamen, and in the chalazal seed coat of ovules and developing seeds. Mutant alleles of SIAR1 accumulate anthocyanins as a symptom of reduced amino acid content in the early stages of silique development. Our data demonstrate that the SIAR1-mediated export of amino acids plays an important role in organic nitrogen allocation and particularly in amino acid homeostasis in developing siliques.

show abstract

“…Mounting genetic proof has characterized these NAC TFs as "master switches" for secondary wall formation in Arabidopsis (Kubo et al, 2005;Zhong et al, 2006Zhong et al, , 2007bYamaguchi et al, 2008). Although WALLS ARE THIN1 (WAT1) might be a regulator of SND1 and NST1 in fiber cells (Ranocha et al, 2010), the upstream signals for secondary wall cellulose synthesis regulation remain largely unknown.…”

Section: Introductionmentioning

confidence: 99%

A Gibberellin-Mediated DELLA-NAC Signaling Cascade Regulates Cellulose Synthesis in Rice

et al. 2015

View full text Add to dashboard Cite

Cellulose, which can be converted into numerous industrial products, has important impacts on the global economy. It has long been known that cellulose synthesis in plants is tightly regulated by various phytohormones. However, the underlying mechanism of cellulose synthesis regulation remains elusive. Here, we show that in rice (Oryza sativa), gibberellin (GA) signals promote cellulose synthesis by relieving the interaction between SLENDER RICE1 (SLR1), a DELLA repressor of GA signaling, and NACs, the top-layer transcription factors for secondary wall formation. Mutations in GA-related genes and physiological treatments altered the transcription of CELLULOSE SYNTHASE genes (CESAs) and the cellulose level. Multiple experiments demonstrated that transcription factors NAC29/31 and MYB61 are CESA regulators in rice; NAC29/31 directly regulates MYB61, which in turn activates CESA expression. This hierarchical regulation pathway is blocked by SLR1-NAC29/31 interactions. Based on the results of anatomical analysis and GA content examination in developing rice internodes, this signaling cascade was found to be modulated by varied endogenous GA levels and to be required for internode development. Genetic and gene expression analyses were further performed in Arabidopsis thaliana GA-related mutants. Altogether, our findings reveal a conserved mechanism by which GA regulates secondary wall cellulose synthesis in land plants and provide a strategy for manipulating cellulose production and plant growth.

show abstract

Walls are thin 1 (WAT1), an Arabidopsis homolog of Medicago truncatula NODULIN21, is a tonoplast-localized protein required for secondary wall formation in fibers

Cited by 170 publications

References 62 publications

Characterizing Regulatory and Functional Differentiation between Maize Mesophyll and Bundle Sheath Cells by Transcriptomic Analysis

Characterizing Regulatory and Functional Differentiation between Maize Mesophyll and Bundle Sheath Cells by Transcriptomic Analysis

Siliques Are Red1 from Arabidopsis Acts as a Bidirectional Amino Acid Transporter That Is Crucial for the Amino Acid Homeostasis of Siliques

A Gibberellin-Mediated DELLA-NAC Signaling Cascade Regulates Cellulose Synthesis in Rice

Contact Info

Product

Resources

About