Abstract:SummaryThe four HD2 proteins of Arabidopsis thaliana (AtHD2A±D) belong to a unique class of histone deacetylases that is plant speci®c. Previously, we have demonstrated that one of the members, AtHD2A, can mediate transcriptional repression when targeted to the promoter of a reporter gene. Here, we report that AtHD2B and AtHD2C can also repress gene expression. AtHD2A and AtHD2C differ from AtHD2B and AtHD2D in the composition of their structural domains. Our data show that both structural types play a role in… Show more
“…Therefore, the most straightforward interpretation of these results is that the elevated expression levels of the CPC and GL2 genes are directly affected by histone hyperacetylation. The down-regulation of WER gene expression hyperacetylation does not fit this pattern, but there are a number of cases where histone hyperacetylation decreases gene expression (29)(30)(31). As expected based on the microarray and semiquantitative RT-PCR results, no discernable changes in the PCR products of the TTG promoters were observed after TSA treatment, although a slight increase in the upstream region of acetylated H4 was detected (Fig.…”
Section: Tsa Treatment Alters Cellular Pattern By Changing the Expressupporting
The Arabidopsis root has a unique cellular pattern in its singlelayered epidermis. Cells residing over the intercellular spaces between underlying cortical cells (H position) differentiate into hair cells, whereas those directly over cortical cells (N position) differentiate into non-hair cells. Recent studies have revealed that this cellular pattern is determined by interactions of six patterning genes CPC, ETC, GL2, GL3͞EGL3, TTG, and WER, and that the position-dependent expression of the CPC, GL2, and WER genes is essential for their appropriate interactions. However, little is known about how the expressions of the pattern genes are determined. Here we show that trichostatin A (TSA) treatment of germinating Arabidopsis seedlings alters the cellular pattern of the root epidermis to induce hair cell development at nonhair positions. The effects of TSA treatment are rapid, reversible, concentration-dependent, and position-independent. TSA inhibition of histone deacetylase activity results in hyperacetylation of the core histones H3 and H4, and alters the expression levels and cell specific expression of the patterning genes CPC, GL2 and WER. Analysis of histone deacetylase mutant cellular patterning further verified the participation of histone acetylation in cellular patterning, and revealed that HDA18 is a key component in the regulatory machinery of the Arabidopsis root epidermis. We propose a working model to suggest that histone acetylation may function in mediating a positional cue to direct expression of the patterning genes in the root epidermal cells.histone as a signaling mediator ͉ trichostatin A ͉ histone deacetylase ͉ positional cue ͉ chromatin immunoprecipitation
“…Therefore, the most straightforward interpretation of these results is that the elevated expression levels of the CPC and GL2 genes are directly affected by histone hyperacetylation. The down-regulation of WER gene expression hyperacetylation does not fit this pattern, but there are a number of cases where histone hyperacetylation decreases gene expression (29)(30)(31). As expected based on the microarray and semiquantitative RT-PCR results, no discernable changes in the PCR products of the TTG promoters were observed after TSA treatment, although a slight increase in the upstream region of acetylated H4 was detected (Fig.…”
Section: Tsa Treatment Alters Cellular Pattern By Changing the Expressupporting
The Arabidopsis root has a unique cellular pattern in its singlelayered epidermis. Cells residing over the intercellular spaces between underlying cortical cells (H position) differentiate into hair cells, whereas those directly over cortical cells (N position) differentiate into non-hair cells. Recent studies have revealed that this cellular pattern is determined by interactions of six patterning genes CPC, ETC, GL2, GL3͞EGL3, TTG, and WER, and that the position-dependent expression of the CPC, GL2, and WER genes is essential for their appropriate interactions. However, little is known about how the expressions of the pattern genes are determined. Here we show that trichostatin A (TSA) treatment of germinating Arabidopsis seedlings alters the cellular pattern of the root epidermis to induce hair cell development at nonhair positions. The effects of TSA treatment are rapid, reversible, concentration-dependent, and position-independent. TSA inhibition of histone deacetylase activity results in hyperacetylation of the core histones H3 and H4, and alters the expression levels and cell specific expression of the patterning genes CPC, GL2 and WER. Analysis of histone deacetylase mutant cellular patterning further verified the participation of histone acetylation in cellular patterning, and revealed that HDA18 is a key component in the regulatory machinery of the Arabidopsis root epidermis. We propose a working model to suggest that histone acetylation may function in mediating a positional cue to direct expression of the patterning genes in the root epidermal cells.histone as a signaling mediator ͉ trichostatin A ͉ histone deacetylase ͉ positional cue ͉ chromatin immunoprecipitation
“…Histone deacetylases and methylases control rDNA genes and thus regulate the epigenetic on/off switch (gene dosage), providing an important mechanism in the biogenesis of ribosomes (25,27). It has been demonstrated that the activity of the yeast RPD3 is required for nucleolar reorganization and RNA pol I delocalization via its association with the rDNA chromatin, which can be antagonized by TOR (13).…”
Section: Discussionmentioning
confidence: 99%
“…The Arabidopsis genome contains four isoforms of the HDT-type histone deacetylases, namely AtHD2A, AtHD2B, AtHD2C, and AtHD2D, among which AtHD2A and AtHD2B share the highest sequence homology and the apparent functional similarities (27)(28)(29). To test the specificity of interaction between RPS6 and the AtHD2B, GFP fusion construct of a fulllength RPS6 (S6FL-GFP) was co-expressed with AtHD2A in protoplasts (Fig.…”
Section: Identification Of Proteins Interacting With the Rps6 Cmentioning
Background: Ribosomal protein S6 has been known to be a key downstream effector of the TOR signaling pathway. Results: We demonstrated that ribosomal protein interacts with a histone deacetylase and binds to rRNA gene promoter.
Conclusion:The TOR signaling controls rRNA synthesis via interaction of RPS6 to rRNA genes. Significance: This study links the environmental signals via TOR kinase to control growth of an organism by regulating ribosome biogenesis.
“…In addition, plants contain an uncommon class of HDACs, the HD2 class, which was identified in plants only (Lusser et al, 1997;Aravind and Koonin, 1998;Wu et al, 2000aWu et al, , 2003Dangl et al, 2001;Zhou et al, 2004). Studies on the mechanism of action of HDACs in plants are beginning to emerge.…”
Histone acetylation is modulated through the action of histone acetyltransferases and deacetylases, which play key roles in the regulation of eukaryotic gene expression. Previously, we have identified a yeast histone deacetylase REDUCED POTASSIUM DEPENDENCY3 (RPD3) homolog, HISTONE DEACETYLASE19 (HDA19) (AtRPD3A), in Arabidopsis thaliana. Here, we report further study of the expression and function of HDA19. Analysis of Arabidopsis plants containing the HDA19:b-glucuronidase fusion gene revealed that HDA19 was expressed throughout the life of the plant and in most plant organs examined. In addition, the expression of HDA19 was induced by wounding, the pathogen Alternaria brassicicola, and the plant hormones jasmonic acid and ethylene. Using green fluorescent protein fusion, we demonstrated that HDA19 accumulated in the nuclei of Arabidopsis cells. Overexpression of HDA19 in 35S:HDA19 plants decreased histone acetylation levels, whereas downregulation of HDA19 in HDA19-RNA interference (RNAi) plants increased histone acetylation levels. In comparison with wild-type plants, 35S:HDA19 transgenic plants had increased expression of ETHYLENE RESPONSE FACTOR1 and were more resistant to the pathogen A. brassicicola. The expression of jasmonic acid and ethylene regulated PATHOGENESIS-RELATED genes, Basic Chitinase and b-1,3-Glucanase, was upregulated in 35S:HDA19 plants but downregulated in HDA19-RNAi plants. Our studies provide evidence that HDA19 may regulate gene expression involved in jasmonic acid and ethylene signaling of pathogen response in Arabidopsis.
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