Identification of T-cadherin as a Novel Target of DNA Methyltransferase 3B and Its Role in the Suppression of Nerve Growth Factor-mediated Neurite Outgrowth in PC12 Cells*

Previously we showed that DNA methyltransferase 3b (Dnmt3b) is required for nerve growth factor (NGF)-induced differentiation of PC12 cells to neuronal phenotype. The present study identified T-cadherin (T-Cad) as one of the targets of Dnmt3b by chromatin immunoprecipitation (ChIP) assay. Combined bisulfite restriction analysis and bisulfite sequencing showed that T-Cad promoter was sparsely methylated in PC12 cells. ChIP-CHOP analysis demonstrated that Dnmt3b is associated with T-Cad promoter irrespective of its methylation status. The mRNA and protein levels of T-Cad were markedly elevated in cells depleted of Dnmt3b by antisense or small interfering RNA. Suppression of T-Cad promoter activity by Dnmt3b was independent of its catalytic activity, which was consistent with the insignificant change in T-Cad promoter methylation status in Dnmt3b-depleted cells. In contrast, deletion of its N-terminal ATRX and PWWP domain abolished its repressor function. Association of histone deacetylase 2 (Hdac2) with T-Cad promoter and restoration of the promoter activity from Dnmt3b-mediated suppression upon treatment with Hdac inhibitor indicated involvement of histone deacetylation in this process. NGF-induced neurite outgrowth was inhibited in a dose dependent manner upon ectopic expression of T-Cad in PC12 cells. Immunofluorescence studies showed that T-Cad was redistributed upon NGF treatment, as evident from its concentration in axon growth cones as opposed to its localization at cell-cell contact region in undifferentiated cells. These results demonstrate a novel role of T-Cad in the NGF-mediated differentiation of PC12 cells to neuronal phenotype.

ture condition, where T-Cad blocks neurite extension of spinal motor neurons both as a substratum and as a soluble recombinant protein (20). A high T-Cad level is also found in cardiac and vascular tissues where aryl hydrocarbon receptor ligands can repress its expression. T-Cad is co-segregated with signaling molecules such as G-protein and SRC family kinase, which implicates its role as an intracellular signaling molecule (25). Interestingly, T-Cad can also function as a receptor for low density lipoprotein and adiponection/Acrp30 (26,27). T-Cad is down-regulated by growth factors such as IGF, EGF, and bDGF in smooth muscle cells (28). The molecular mechanism for its down-regulation by these growth factors has not been elucidated. The identification of T-Cad as one of the target genes of DNA methyltransferase 3b coupled with increased expression of this DNA methyltransferase during differentiation of PC12 cells provided an important experimental system to study the function of T-Cad in the differentiation process. The present study addresses the mechanism by which Dnmt3b suppresses T-Cad expression and the role of T-Cad in NGF-induced differentiation of PC12 cells.

EXPERIMENTAL PROCEDURES
Reagents and Antibodies-Trichostatin A (TSA) was from Sigma. NGF was from Roche Applied Science. Anti Dnmt3b antibody was raised in our laboratory as described previously (29). Anti-T-Cad and anti-HDAC2 antibodies were from Santa Cruz Biotechnology. Anti-MYC and anti-FLAG (M2) antibodies were from Sigma and anti-Ku-70 antibody (N3H10) was from Neomarker.
Cell Line and Tissue Culture-PC12 cells were cultured and treated with NGF as described earlier (16).

Construction of Plasmids and Generation of Stable Cell Lines-T-Cad-FLAG (T-CadFLAG)
: T-Cad cDNA was amplified from mouse lung cDNA library (primers 5Ј-CGG GAT CCC TTC TAG TCG GGC AAG ATG CA, and 5Ј-CGG AAT CCT CAC AGA CCT GAC AAT AAG CTG A). The PCR product was phosphorylated and ligated to the EcoRV site of pcDNA3.1(Ϫ) to generate T-Cad-pcDNA3. The authenticity of the clone was verified by sequencing. Next, T-Cad was PCRamplified from T-Cad-pcDNA3 with the same forward primer and 5Ј-CGGGATCCCAGACCTGACAATAAGCTGA as the reverse primer digested with BamHI and was cloned into the same site of pCMV-3ϫFLAG (Sigma) to generate T-CadFLAG. To obtain T-Cadexpressing cells, T-CadFLAG was transfected into PC12 cells and selected with G418 (500 g/ml). Expression of T-Cad in stable cell lines was verified by Western blot analysis with anti-FLAG M2 antibody.
T-Cad Promoter-Luciferase Reporter Gene (pT-CadGL2)-T-Cad promoter was PCR-amplified from PC12 cell genomic DNA with primers 5Ј-CGG GGT ACC CAG AGT CTG GGC AAC ATG CTG T and 5Ј-CCG CTC GAG TGC GGC TCA CAT TCC CTA CCTG and cloned into the KpnI and XhoI site of pGL2 basic plasmid (Promega).
Dnmt3b-⌬PWWP-PWWP domain deletion mutant of Dnmt3b was generated by PCR as described earlier (16) with the primers 5Ј-GG GGT ACC ACC ATG ATC TCT GCT GAC AAA CTG GTG and 5Ј-CG GGA TCC TTC ACA GGC AAA GTA GTC CTT. The PCR product was cloned into KpnI and BamHI sites of pCMV-3ϫFLAG (Sigma).
Western Blot Analysis-Cellular proteins were extracted with cell lysis buffer (50 mM Tris-HCl, pH 7.5, 10% glycerol, 2% SDS, and 1 mM dithiothreitol) or as indicated. The extract was resolved by SDS-PAGE, transferred to the nitrocellulose membrane, and subjected to immunoblot analysis.
Real-time Quantitative RT-PCR and RT-PCR-Total RNA was isolated from PC12 cells using acid guanidinium thiocyanate-phenol method (30) and was treated with Turbo DNase 1 (Ambion) following manufacturer's protocol. cDNA was synthesized from 1 g of total RNA using random hexamers as primers and murine leukemia virus reverse transcriptase following the manufacturer's protocol (Applied Biosystem). An aliquot of the cDNA (equivalent to 100 ng of RNA T-Cad and 2 ng for 18 S rRNA) was used for real-time PCR analysis. All reactions were carried out using the Mx3000 Multiplex quantitative PCR system (Stratagene) as described previously (16). The PCR primers used for RT-PCR analysis were 5Ј-AAA CCT CAG CGT GGT CAT CCT and 5Ј-GCG TGG GTG TTG TTG ATT TTG for amplification of T-Cad and TCA AGA ACG AAA GTC GGA GG and GGA CAT CTA AGG GCA TCA CA for 18 S rRNA. RT-PCR analysis of Dnmt3b and COX-1 (cytochrome c oxidase) was as described previously (16).
COBRA and Bisulfite Genomic Sequencing-Cells were treated with bisulfite reagent as described (31). T-Cad CpG island (CGI) located at proximal promoter and exon 1 was amplified by nested PCR with primer set #1 (proximal promoter) (5-GGT TGG ATT TTA GGA GTA AAA and AAA ACC AAC CTT TAA AAA AAA) and set #2 (exon) (5-TAT TTG GGA AGT TGG TTG G and 5-CTC ACA TTC CCT ACC TAA AAC). The PCR products were purified and digested with BstUI or TaqI to determine the methylation status. Tsp509I was used to verify the completion of bisulfite conversion. For bisuifite sequencing, the PCR products were cloned into TOPO-TA vector (Invitrogen), and purified plasmid from five individual clones from each set were sequenced. The construction of ⌬ATRX and ⌬N-Dnmt3b was described earlier (16).
ChIP and ChIP-CHOP Analysis and Sequencing-ChIP assay was performed as described earlier (9,32). Cells were cross-linked with 1% formaldehyde for 10 min followed by sonication of cell lysate that was precleared with preimmune serum for Dnmt3b or protein G-agarose A beads for Hdac2. Dnmt3b or Hdac2 associated protein-DNA complex was pulled down by anti-Dnmt3b or anti-Hdac2 antibody, respectively, followed by extensive washing. Eluted DNA was dissolved in radioimmune precipitation assay buffer and subjected to one more round of immunoprecipitation with the same antibody to minimize nonspecific pull-down. To identify Dnmt3b target genes the DNA fragments pulldown by Dnmt3b were subjected to end filling/repairing with Klenow and subsequently cloned into the SmaI site of pBlueScript-SKϩ to allow blue white color selection. Individual clones were identified by automated sequencing. The identity of the potential genes was established with gene analyzing tools and gene databases (BLAST: www.ncbi.nlm. nih.gov/BLAST; BLAT: genome.ucsc.edu/cgi-bin/hgBlat; SOURCE: genome-www5.stanford.edu/cgi-bin/source/; Uniprot: www.expasy. uniprot.org/). The primers used to amplify the T-Cad promoter were 5Ј-AGG GAG CGT TAT GAA GGA ATCC and 5Ј-GAG GAG GCG AAC CAA AGT TACC. The primers used for GAPDH promoter were 5Ј-TCA GCG GGT GTT GTT TGT GTCC and 5Ј-TTT GCG TGC GTG TGT GTC TG. The primers used for PI3K promoter were TCC GCT TTT GTG GAG ATA CCG and AAC TGC TGT TGG AAG TAG TGT CCC. For CHIP-CHOP analysis, the Dnmt3b pulled down DNA, and input DNA were digested with either HpaII (methylation-sensitive) or its isoschizomer MspI (methylation-insensitive) followed by PCR analysis with the same primers.
In Vitro DNA Methylation-The protocol used for the site-specific methylation of T-Cad was as described (33).
Transient Transfection and Luciferase Assay-PC12 cells were plated at a density of 5 ϫ 10 5 /12-well plate, transfected with T-Cad promoter (pT-cadGL2 along with Dmt3b or empty vector using Lipofectamine 2000 TM (Invitrogen). Cells were harvested 48 h post-transfection followed by the luciferase reporter assay in the cell lysate (29). Transfection of Dnmt3b siRNA was performed as described (16).

RESULTS
T-Cad Is a Dnmt3b Target Gene in PC12 Cells-To explore the molecular mechanism of Dnmt3b-mediated differentiation of PC12 cells, we identified the potential targets in these cells. For this purpose, the Dnmt3b-DNA complex was immunoprecipitated with Dnmt3b antibody and the purified DNA was cloned into pBSKϩ. Approximately 120 clones were sequenced. The identity of the potential target genes was established by data base analysis. Based on their known or postulated function, Dnmt3b target genes were classified into five categories, namely, cell matrix/transmembrane proteins, proteins specific to brain/ neuron, signaling transduction, cell cycle progression, and transcriptional regulation (see supplemental Table S1). Approximately 10% of the pulled down sequences were ALU repeats, single repeats, or long terminal repeats (not listed).
We selected one of the target genes, T-Cad, for further study based on the important role of the encoded protein in cell-cell adhesion, cell signaling, embryogenesis, and in motor neuron axon growth (20,17,34). The association of Dnmt3b with T-Cad promoter in PC12 cells was verified by chromatin immunoprecipitation followed by PCR analysis. T-Cad promoter was specifically amplified from the DNA immunoprecipitated with Dnmt3b antibody but not from the DNA pulled down from preimmune serum. The result showed that Dnmt3b was indeed associated with T-Cad promoter (Fig. 1A). Furthermore, the lack of association of Dnmt3b with the GAPDH promoter, a housekeeping gene, confirmed its specific association with T-Cad promoter (Fig. 1A). . T-Cad mRNA was also up-regulated in cells depleted of Dnmt3b using siRNA (Fig. 1C, top panel). The level of T-Cad 48h posttransfection increased proportionately (ϳ2-fold) with the concentration of Dnmt3b siRNA used, whereas the same amount of scrambled siRNA did not have any significant effect. The increase in T-Cad mRNA level after 72 h was less pronounced (Fig. 1C, top panel), which is consistent with the increase in Dnmt3b mRNA (Fig. 1C, middle panel) probably due to decrease in intracellular siRNA level with time. No significant alteration in Dnmt3b protein level was detected in scramble siRNA transfected cells compared with that of the parental cells whereas its level was reduced by 75% in Dnmt3b-siRNA transfected cells (Fig. 1C, bottom panel). Western blot analysis showed that T-Cad protein level significantly increased upon Dnmt3b depletion in PC12 cells (Fig. 1D) that correlated with increase in its mRNA level (Fig. 1, B and C). These results demonstrate that Dnmt3b negatively regulates T-Cad expression. Dnmt3b level was not altered in vector-transfected cells compared with that of parental cells (data not shown).

T-cadherin CGI Is Partially Methylated in PC12 Cells, Which Is Not
Significantly Altered upon Dnmt3b Depletion-To identify the underlying mechanism of Dnmt3b-mediated down-regulation of T-Cad expression, we first investigated whether Dnmt3b regulates the methylation status of T-Cad promoter in PC12 cells. To address this issue, we performed COBRA (combined bisulfite-restriction analysis) of T-cad promoter CGI in the vector-transfected and Dnmt3b depleted PC12 cells. Bisulfite treatment of DNA converts unmethylated cytosines to uracils, whereas methylated cytosines remain unaffected. Upon subsequent PCR, uracils and methylcytosines are amplified as thymine and cytosines, respectively. The amplified PCR product from only methylated DNA could be digested by enzymes such as TaqI (TCGA) or BstUI (CGCG) due to retention of cytosine. The PCR products obtained from two regions of the T-Cad CGI spanning the proximal promoter (Ϫ220 to Ϫ38) and first exon (Ϫ38 to ϩ96) ( Fig. 2A) were digested with these enzymes. The results showed that the promoter was partially digested with these enzymes demonstrating partial methylation (Fig. 2B, left and middle panels). The methylation of proximal promoter was significantly less (ϳ20%) than that of exon 1 (ϳ40%) (Fig. 2B, left and middle panels). Complete digestion of the PCR products with Tsp509I confirmed complete bisulfite conversion (Fig. 2B, right panel). It is noteworthy that the

Dnmt3b Represses T-cadherin Expression
extent of digestion of the PCR product obtained from Dnmt3b-depleted cells with BstUI (Fig. 2B, left panel) or TaqI (Fig. 2B, middle panel) was comparable with that of vector-transfected cells. To determine the methylation profile of individual CpG base pairs within the CGI of T-Cad, bisulfite genomic sequencing was performed (Fig. 2C). The sequence analysis revealed sparse methylation of CpGs in the proximal promoter region and comparatively dense methylation of CpGs in the exon 1 in both Dnmt3b-depleted cells and vector-transfected control cells (Fig. 2C), which corroborated the COBRA data (Fig. 2B). These results suggest that T-Cad CGI is not heavily methylated in PC12 cells, which is maintained in the absence of Dnmt3b probably by Dnmt1 and/or Dnmt3a.
Partial methylation of T-Cad promoter raised the question whether Dnmt3b is preferentially associated with the methylated promoter. To address this issue ChIP-CHOP assay was performed. DNA pulled down with preimmune sera or Dnmt3b antibodies was either undigested or digested with HpaII or MspI. The input DNA was digested in parallel. An aliquot of the digested DNA was amplified with primers spanning the HpaII/MspI site on the CGI. The amount of PCR product from HpaII-digested DNA (methylated promoter) was 40% of that obtained from the undigested DNA (both methylated and unmethylated promoter) pulled down by Dnmt3b antibody (Fig. 3, B and C). These data suggest that Dnmt3b is associated with both methylated and unmethylated T-Cad promoter. Absence of PCR product from the DNA precipitated by preimmune sera and lack of amplification of GAPDH promoter showed the specificity of this assay (Fig. 3B).
PWWP and ATRX Domains of Dnmt3b Mediate Its Inhibitory Activity on the T-Cad Promoter-Since Dnmt3b is associated with T-Cad promoter irrespective of its methylation status, it was important to determine whether it regulates activity of both promoters. To test this possibility, T-Cad promoter was amplified from PC12 genomic DNA and cloned into luciferase reporter vector (pT-cadGL2). The cloned T-Cad promoter encompasses two HpaII sites, which were in vitro methylated with HpaII methylase to generate methylated promoter.
Mock-methylated or HpaII-methylated T-Cad promoter was co-transfected with the wild type or different mutants of Dnmt3b (Fig. 4A). The T-Cad promoter-driven luciferase activity was significantly impeded (ϳ50%) when the promoter was methylated at HpaII sites (Fig. 4B,  upper panel, lanes 1 and 4). Ectopic expression of Dnmt3b further inhibited the activity of the promoter irrespective of its methylation status (lanes 2 and 5). The extent of inhibition of Dnmt3b on both promoters was comparable (55 and 58% on mock-methylated and methylated promoters, respectively). It is noteworthy that the inhibitory  effect of the catalytic site (CS) mutant of Dnmt3b on both T-Cad promoters was similar (ϳ60%) to that of the wild type protein (lanes 3 and  6). The level of the ectopic wild type and CS mutant Dnmt3b was also comparable (Fig. 4B, lower panel). These results indicate that Dnmt3b suppresses T-Cad promoter activity irrespective of its methylation status and its catalytic activity is not required for this process. Furthermore, the extent of repression of T-Cad promoter activity increased with increasing amount of transfected Dnmt3b expression vector (Fig. 4C).
To determine whether the transfected T-Cad promoter is methylated de novo upon ectopic expression of Dnmt3b, the reporter plasmid (pT-cadGL2) was isolated from PC12 cells co-transfected with Dnmt3b expression vector or the corresponding empty vector. The plasmid DNA was subjected to digestion with methylation sensitive restriction enzyme HpaII, AciI, or methylation-insensitive MspI, followed by PCR analysis with T-Cad-specific forward primer and pGL2 specific reverse primer. Lack of amplification of the T-Cad promoter fragment from HpaII-or AciI-digested plasmid DNA showed that the promoter was not methylated when co-expressed with Dnmt3b or empty vector (Fig.  4D). These results further prove that the Dnmt3b-mediated suppression of T-Cad promoter activity does not involve promoter methylation. Furthermore, inability of 5-azacytidine to increase basal expression of the endogenous and transfected T-Cad promoter (data not shown) supports the notion that methylation does not regulate its expression in PC12 cells, although its promoter is sparsely methylated (Fig. 2C). Apart from the catalytic domain, Dnmt3b harbors a relatively larger N-terminal region that encompasses PWWP and ATRX domains (Fig.  4A). Although PWWP domain of Dnmt3b exhibits DNA binding property (35), Dnmt3b can still binds to DNA in its absence (36). It is also involved in protein-protein interaction (37,38). The ATRX domain is homologous to the ATRX gene, a member of the SWI/SNF family of chromatin remodeling proteins (39). ATRX domain can recruit histone deacetylases (Hdacs) and other transcriptional co-repressors to inhibit gene expression (40,41). To investigate the potential involvement of these domains in the repressor function of Dnmt3b, pT-cadGL2 was co-transfected with ⌬ATRX or ⌬PWWP mutants. The inhibitory effect of Dnmt3b on the promoter activity was partially recovered upon deletion of PWWP or ATRX domain (Fig. 4E, inhibition of mock-methylated promoter was 61 and 37%, respectively, versus 79% by the wild type; methylated promoter was 42 and 30%, respectively, versus 58% by the wild type). Western blot analysis demonstrated comparable expression of Dnmt3b variants (Fig. 4, B and E). The partial reversal of its inhibitory effect on T-Cad promoter upon deletion of these domains suggests that both PWWP and ATRX domain are essential for the repressor function of Dnmt3b on T-Cad promoter irrespective of its methylation status. These results were further confirmed by ectopic expression of the entire N-terminal deletion mutant of Dnmt3b (⌬N), where its inhibitory effect on T-Cad promoter was abolished (Fig. 4F). The inhibitory effect of Dnmt3b on T-Cad promoter varied slightly between experiments (Fig.  4, B and E), which was possibly due to differential expression of Dnmt3b.
Hdac2 Is Associated with T-Cad Promoter, and the Inhibitory Activity of Dnmt3b on the Promoter Can Be Relieved by Treatment with TSA, a Hdac Inhibitor-The involvement of ATRX domain of Dnmt3b in the repression of T-Cad suggested to us the potential involvement of Hdac as a co-repressor. Our earlier study demonstrated Dnmt3b physically and functionally interact with Hdac2 in PC12 cells differentiated by NGF (16). To investigate whether Hdac2 plays a role in the regulation of the expression of T-Cad, we performed ChIP assay with Hdac2 specific antibody. Indeed, Hdac2 was associated with T-Cad promoter (Fig. 5A,  upper panel, lane 3). No PCR product was detected when protein G-agarose beads alone were used for the assay (lane 2). Lack of amplification of PI3K promoter further showed the specificity of this association (Fig. 5A, lower panel). Next, we measured T-Cad mRNA level in cells treated with TSA. The result showed dramatic increase (ϳ25-fold) in T-Cad mRNA upon treatment with TSA (Fig. 5B). Similarly, TSA treatment also activated the trasfected promoter by 4.5-fold (Fig. 5C) suggesting that Hdacs also regulate the activity of the promoter. Significantly less activation of the ectopic promoter compared with that of the mRNA level is probably due to the availability of a small fraction of the transfected promoter in the nucleosomal structure. Alternatively, the transfected promoter (ϳ1.6 kb) cannot execute full function due to lack of some regulatory elements. However, the results demonstrate that both endogenous and the transfected promoters are regulated by Hdacs. The next obvious question was whether Dnmt3b repressed T-Cad by recruiting Hdac. A 7.6-fold increase in T-Cad promoter activity in Dnmt3b transfected cells upon TSA treatment showed that suppression of histone deacetylatase activity could overcome the inhibitory activity of Dnmt3b on the promoter (Fig. 5C). This result suggests that the recruitment of Hdac(s), probably Hdac2, by Dnmt3b is essential to repress the T-Cad promoter.
T-Cad Inhibits NGF-induced Neurite Outgrowth in PC12 Cells-To investigate the potential role of T-Cad in NGF-induced PC12 cell differentiation, stable cell lines constitutively expressing FLAG-tagged T-Cad (T-CadFLAG) were generated. Two cell lines expressing low (T-Cad1) and high (T-Cad2) levels of T-Cad (Fig. 6A) were used for further studies. First, the neuronal differentiation was examined in these cells treated with NGF for up to 6 days and compared with that of vector-transfected (control) cells. Neurite outgrowth was visible within 24 to 48 h of NGF treatment in control cells (Fig. 6A). In contrast, both T-Cad1 and T-Cad2 cells exhibited a tendency to grow in clusters and responded poorly to NGF treatment (Fig. 6, B and C). After prolonged NGF exposure, neurite outgrowth was observed only at the periphery of the clusters in T-Cad-expressing cells, and the extent of neurite formation was inversely correlated with the level of T-Cad expression (Fig. 6, B and C). Thus, T-Cad1 cells (low T-Cad level) exhibited twice as much neurite outgrowth as T-Cad2 cells (high T-Cad level) (Fig. 6, B and C) after 6 days of NGF exposure. This result suggests that T-Cad impedes NGF-induced neurite outgrowth.

T-Cad Is Redistributed from Cell-Cell Contact Region to Neurite Growth Cones in Differentiated Cells
-T-Cad is predominantly an extracellular protein associated with the plasma membrane through GPI anchor. Because NGF-induced differentiation of PC12 cells causes profound changes on the plasma membrane that include membrane depolarization (42) and translocation or redistribution of membranebond signaling molecules such as TrkA (43), PKC␣ (44), and inositol polyphosphate 5-phosphatase (PIPP) (45), we examined the localization of T-Cad after NGF treatment. T-Cad exhibited punctate staining at the plasma membrane and dense staining was observed at cell-cell contact in untreated cells (Fig. 7, A and C), which indicated its concentration at the cell-cell contact points. Strikingly, T-Cad was redistributed upon NGF treatment as demonstrated by its localization at neurite growth cones and growing axon processes (Fig. 7, D and F, G and I, and J and L). The redistribution of T-Cad to growth cone in response to NGF might have a role in its inhibition of neurite outgrowth in PC12 cells.

DISCUSSION
The present study explored the role of T-Cad in neuronal differentiation using NGF-mediated neurite outgrowth in PC12 cells as the model system. Specific increase in Dnmt3b level, one of the three functional DNA methyltransferases, reported in our earlier study (16) and the present observation that T-Cad is one of the Dnmt3b target genes prompted us to explore the functional significance of this finding. Interestingly, Dnmt3b suppressed T-Cad expression with no significant effect on its promoter methylation. Furthermore, depletion of Dnmt3b from PC12 cells enhanced its expression, which correlated with continued proliferation of the cells in the presence of NGF (16). This result reinforces the notion that T-Cad functions as a negative signal in neuronal differentiation. In this context, it is noteworthy that T-Cad functions in initiating proliferation in vascular cells and that it may facilitate progression of proliferative vascular disorders (46). There are also indications that human T-Cad is involved in lung metastasis of osteosarcomas (47). The abundant expression of T-Cad in undifferentiated or metastatic cancer cells is consistent with the lack of or markedly reduced expression of T-Cad in differentiated sympathetic neurons in vivo (20) and in differentiated PC12 cells observed in the present study.
The molecular mechanism underlining T-Cad-mediated inhibition of neurite outgrowth remains to be resolved. It appears that it can function as a negative regulator of axon growth. It is expressed in the region devoid of extending growing motor axons during chick embryo hind limb projection, which implicates that T-Cad functions as an inhibitory factor for motor axon growth (48). The present study showed re-distribution of T-Cad during NGF-induced differentiation of PC12 cells as shown by its strong staining in restricted membrane region and growing axon processes after NGF treatment in contrast to dense staining at cell-cell contact region. This observation together with the finding that its overexpression inhibits neurite outgrowth suggests that T-Cad functions as a negative navigator for axon guidance during NGF-induced neuronal differentiation. The high level of T-Cad in the cerebral cortex, medulla oblongata, and nucleus olivaris relative to its absence from granular cells (19) suggests that it may play an important role in specific neural growth. Exploration of its regulation will help us understand its function.
The suppression of T-Cad by Dnmt3b independent of its enzymatic function merits discussion. All DNA methyltransferases consist of the catalytic domain at their C termini and a transcription repressor domain at their N termini. Through their N-terminal domains, Dnmts transcriptionally repress gene expression by recruiting transcriptional co-repressors and chromatin remodeling enzymes in a methylation independent manner (5,41,49,50). Dnmt3L, a Dnmt3 family member devoid of intrinsic DNA methyltransferase activity due to lack of the catalytic motif, can also function as a transcriptional repressor (51).
Although T-Cad is a Dnmt3b target gene its promoter region is sparsely methylated (Fig. 2), and its expression is not induced after treatment of the differentiated PC12 cells with the potent DNA hypomethylating agent, 5-AzaC (data not shown). The lack of requirement of the catalytic activity of Dnmt3b in T-Cad promoter repression further reinforces the notion that Dnmt3b regulates expression of this gene by methylation independent mechanisms. Restoration of T-Cad expression by an Hdac inhibitor suggests that histone deacetylation plays a significant role in its suppression. Since genes suppressed by methylation are not re-activated by Hdac inhibitors in the absence of a DNA hypomethylating agent (9,52), up-regulation of T-Cad expression by TSA alone further proves the concept that suppression of the cadherin protein by Dnmt3b in PC12 cells is independent of its DNA methyltransferase activity.
Finally, the specific function of T-Cad deserves comments. The present study established it as a possible negative regulator of axon growth in neuronal differentiation. T-Cad expression is enhanced in some cancers such as metastatic lung cancer (47), whereas its expression is significantly down-regulated in other cancers like colorectal cancer, breast cancer, and skin cancers, probably mediated by promoter methylation (53)(54)(55)(56). It would be of interest to investigate its role in brain tumorigenesis. Nevertheless, these findings have demonstrated an important role of T-Cad in altering the differentiated state that contributes to FIGURE 7. T-Cad redistribution occurs concomitantly with NGF treatment. T-Cadexpressing PC12 cells either untreated or treated with NGF for 24 -96 h were stained with anti-FLAG M2 antibody (to detect FLAG-tagged T-Cad, red) and 4Ј,6-diamidino-2-phenylindole (DAPI) (to locate the nucleus, blue) and visualized under fluorescence microscope. The arrow indicates strong staining of T-Cad.

Dnmt3b Represses T-cadherin Expression
cancer and has provided the impetus to explore the molecular mechanism of T-Cad signaling as well as regulation of its expression.