当前位置: 首页 > 期刊 > 《核酸研究》 > 2006年第9期 > 正文
编号:11121664
GAS41 interacts with transcription factor AP-2? and stimulates AP-2?-mediated transactivation
http://www.100md.com 《中华首席医学网》
     ABSTRACT

    Transcription factor AP-2 regulates transcription of a number of genes involving mammalian development, differentiation

    and carcinogenesis. Recent studies have shown that interaction partners can modulate the transcriptional activity of AP-2

    over the downstream targets. In this study, we reported the identification of GAS41 as an interaction partner of AP-2?. We

    documented the interaction both in vivo by co-immunoprecipitation as well as in vitro through glutathione S-transferase (GST)

    pull-down assays. We also showed that the two proteins are co-localized in the nuclei of mammalian cells. We further mapped

    the interaction domains between the two proteins to the C-termini of both AP-2? and GAS41, respectively. Furthermore, we have

    identified three critical residues of GAS41 that are important for the interaction between the two proteins. In addition, by

    transient co-expression experiments using reporter containing three AP-2 consensus binding sites in the promoter region, we

    found that GAS41 stimulates the transcriptional activity of AP-2? over the reporter. Finally, electrophoretic mobility shift

    assay (EMSA) suggested that GAS41 enhances the DNA-binding activity of AP-2?. Our data provide evidence for a novel cellular

    function of GAS41 as a transcriptional co-activator for AP-2?.

    INTRODUCTION

    To date, five members of the AP-2 family of transcription factors, AP-2, AP-2?, AP-2, AP-2 and AP-2, have been

    identified. The AP-2, AP-2?, AP-2 genes are relatively well characterized (1–6). The AP-2 protein forms a unique modular

    structure consisting of an N-terminal proline- and glutamine-rich transactivational domain and a complex helix-span-helix

    motif necessary and sufficient for dimerization and site-specific DNA binding (7,8). A number of genes that mediate cell

    growth, cell shape, cell movement, cell fate and cell communication frequently possess the AP-2 binding site in their cis-

    regulatory sequences (9–15). Several genes related to cancers have also been shown to be regulated by AP-2, such as erbB-2

    (3,10,16,17), ER (12) and IGF IR (16,18) in breast cancer, and MUC18 and c-KIT genes in melanoma (19,20). The AP-2 family of

    genes also plays important roles in mammalian development. AP-2 genes show overlapping but distinct patterns of expression

    during vertebrate embryogenesis, and function in the development and differentiation of the neural tube, neural crest

    derivatives, heart, skin, urogenital tissues and extraembryonic trophoblasts (21–23). The importance of AP-2 genes is

    highlighted by knockout experiments of AP-2, AP-2? and AP-2. Mice lacking both copies of AP-2 gene die perinatally and

    exhibit at least six major defects during embryogenesis: morphogenesis of the neural tube, face, eye, body-wall,

    cardiovascular system and forelimbs (24–27). Mice lacking AP-2? display fewer gross phenotypic defects but die shortly after

    birth due to the disruption of terminal kidney differentiation (28). The AP-2-null mice die around E7.5, shortly after

    implantation due to the defects within the extraembryonic cell lineages (23,29).

    The AP-2 family of transcription factors plays a broad range of roles from cell growth, tissue morphogenesis and cancers.

    One of mechanisms for the AP-2 family fulfills their roles is to activate or suppress various downstream target genes at

    transcriptional levels. A number of studies demonstrated that AP-2-interacting proteins can affect the transcription of AP-2

    downstream targets by modulating the transcriptional activity of AP-2. In fact, several AP-2-interacting partners have been

    identified. For example, the transactivation of p21WAF1 by AP-2 was augmented while activation of laminin receptor by AP-2

    was reduced through a direct interaction with p53 (30,31). AP-2 represses the transactivation by Myc through associating with

    Myc and competing the binding site with Myc (11). Other AP-2-interacting proteins include Yin Yang factor 1 (YY1) (32),

    retinoblastoma protein (RB) (33,34) and oncogene DEK (35). Wwox tumor suppressor protein was also identified as an AP-2

    interacting partner, and Wwox protein triggers redistribution of nuclear AP-2 to the cytoplasm, hence suppressing AP-2-

    mediated transactivation (36).

    To date, no AP-2?-interacting factor has been reported yet. To search for AP-2?-interacting proteins, we used AP-2? as

    the bait and screened a HeLa cDNA library in yeast two-hybrid system. We identified GAS41 as a protein partner of AP-2?. The

    interaction between the two proteins was confirmed in vivo by co-immunoprecipitation and co-localization assays, and

    demonstrated in vitro by glutathione S-transferase (GST) pull-down assay. The interaction domains between the two proteins

    were mapped to the C-terminus of AP-2? and C-terminus of GAS41. Furthermore, we demonstrated that GAS41 resulted in

    enhancement of transcriptional activity of AP-2? over AP-2 response element reporter by, at least in part, enhancing the DNA

    -binding activity of AP-2?.

    MATERIALS AND METHODS

    Vector construction

    For yeast two-hybrid screening, full-length cDNA of AP-2? was ligated in frame with the GAL4 DNA-binding domain of the

    pDBLeu vector resulting in pDBLeu/AP-2?. For immunoprecipitation and colocalization assays, the full-length cDNA of AP-2? was

    cloned into the mammalian expression plasmid pCMV-Myc vector (Clontech), forming a Myc tagged AP-2? expression vector pCMV-

    Myc-AP-2?, while full-length cDNA and the mutations of GAS41 were inserted into pCMV-HA vector (Clontech), forming a HA

    tagged GAS41 expression vector pCMV-HA-GAS41, and full-length cDNA of GAS41 was also cloned into pCMV-Myc vector. Vector

    pGEX-4T-2 (Amersham) was used to construct vectors expressing GST-AP-2? fusion proteins. The cDNA fragments encoding full-

    length and subdomains (Figure 3G) of AP-2? were cloned in frame with respect to GST into pGEX-4T-2 individually. Plasmid pQE

    -N3 (Qiagen) was used to generate vectors expressing His-tagged GAS41 fusion proteins. The cDNAs encoding full-length

    subdomains (Figure 4F) and point mutations of GAS41 were fused in frame to His tag of pQE-N3 individually. Reporter plasmid

    A2-Luc was constructed by replacing CAT gene with luciferase gene in pA2BCAT vector (generous gift of T. Williams) which

    contains three copies of AP-2 binding site in human metallothionein IIa gene in the promoter region (7). Vector pCMV-LacZ was

    constructed by fusing LacZ gene into pCMV-Myc.

    Yeast two-hybrid screens

    The pro yeast two-hybrid system was obtained from GIBCO/BRL. A HeLa cDNA library cloned in frame with the GAL4 activation

    domain in the vector pPC86 was used to screen AP-2?-interacting clones. The MaV203 yeast strain was transformed with the

    pDBLeu-AP-2? and tested for a basal expression activity, as described in the GIBCO/BRL protocol. The bait-containing MaV203

    cells were subsequently transformed with the HeLa cDNA library, and transformants were selected by growing SD-leu–, Trp–,

    Ura–, His– medium supplemented with 25 mM 3-amino-1, 2, 4-triazole (3-AT). False positive clones were eliminated by

    retransforming the prey DNA to the original bait strain and positive clones were further verified using X-gal filter assay.

    Finally, plasmids from positive clones were sequenced and characterized.

    Cell culture and transient transfections

    HeLa cells and human HepG2 cells were cultured in DMEM supplemented with 10% fetal bovine serum, penicillin (100 U/ml)

    and streptomycin (100 μg/ml). The cells were cultured at 37°C in a 5% CO2 incubator. Cells were transfected at 70%

    confluence using the Lipofectamine 2000 (Invitrogen) according to the manufacturer's instructions.

    Immunoprecipitation and western blot analysis

    HeLa cells were co-transfected with pCMV-Myc-AP-2? and pCMV-HA-GAS41 or only transfected with pCMV-Myc-AP-2?. Twenty four

    hours after transfection, HeLa cells were lysed in RIPA buffer [50 mM Tris–HCl (pH 7.2), 150 mM NaCl, 1% (v/v) Triton X-100,

    1% (w/v) sodium deoxycholate, 0.1% (w/v) SDS] with protease inhibitors. Immunoprecipitation using either mouse monoclonal

    anti-Myc antibody or rabbit polyclonal anti-HA antibody (Santa Cruz Biotech) were performed as described previously (37). Co

    -precipitated proteins were subjected to electrophoresis on 13% SDS–polyacrylamide gel, and were then analyzed by western

    blot analysis using rabbit polyclonal anti-HA antibody, monoclonal anti-Myc antibody or rabbit polyclonal anti-GAS41 antibody

    (Santa Cruz Biotech).

    Immunofluorescent staining

    HeLa cells were cultured on glass coverslips and transfected with pCMV-Myc-AP-2? and pCMV-HA-GAS41. Twenty four hours

    after transfection, cells were fixed with 4% (w/v) paraformaldehyde in phosphate-buffered saline (PBS) for 10 min, and

    permeabilized with 0.2% Triton X-100 for 5 min. Cells were then incubated with primary antibodies diluted in PBS with 1%

    (v/v) normal goat serum for 1 h and with the secondary antibodies under the same conditions. The primary antibodies used were

    mouse monoclonal anti-Myc and rabbit polyclonal anti-HA antibodies (Clontech) while the secondary antibodies were Alexa 594

    goat anti-mouse and Alexa 488 goat anti-Rabbit antibodies (Molecular Probes). Hoechst 33 258 (Sigma) was used to stain the

    nuclei. Fluorescence on the processed slips was analyzed using a confocal laser microscope (Radiance 2100, BioRad).

    GST pull-down assay

    GST, GST-AP-2? and other GST fusion proteins, His-GAS41 and other His fusion proteins were expressed and purified

    according to manufacturer's instructions (Amersham). For the pull-down assay, 1–5 μg of the GST or GST fusion proteins were

    mixed with 40 μl of 50% suspension of glutathione-Sepharose 4B beads for 2 h in binding buffer [25 mM HEPES-NaOH (pH 7.5),

    12.5 mM MgCl2, 10% Glycerol, 5 mM DTT, 0.1% NP-40, 150 mM KCl and 20 μM ZnCl2]. Then 1–5 μg of His fusion proteins were

    added followed by incubation for another 2 h. The pellets were washed extensively and boiled. The bound proteins were

    resolved by 13% SDS–polyacrylamide gel and analyzed by western blot analysis with mouse monoclonal anti-His antibody (Santa

    Cruz Biotech).

    Luciferase assays

    Transient transfections of cells with A2-Luc, pCMV-LacZ and the indicated expression vectors were carried out with

    Lipofectamine 2000 (Invitrogen). Twenty four hours after transfection, the cells were lysed and luciferase assay was

    performed using the luciferase assay system (Promega). pCMV-LacZ was cotransfected in all experiments, and ?-galactosidase

    activity was used to normalize for different transfection efficiencies.

    Electrophoretic mobility shift assay (EMSA)

    The consensus AP-2 binding site in human metallothionein IIa promoter was used for EMSA. The oligonucleotide sequences

    used for EMSA were as follows. Forward, 5'-TGACCGCCCGCGGCCCGTG-3'; reverse, 5'-CACGGGCCGCGGGCGCTCA-3'. The binding

    specificity was determined using the AP-2 binding site within the PDIP1 promoter, Sp1 binding site in SV40 promoter and SV40

    oligo containing no binding site for transcription factor as specific and non-specific cold competitor DNA, respectively. The

    upper oligonucleotide sequences were shown, AP-2: 5'-GACGCGGCCCTCGGCCTGGCC-3', Sp1: 5'-GCGCTGGGGCGGCTGGTGGACG-3', SV40: 5'-

    ATTCGATCGGGGCGGGGCGAGC-3' (38). The EMSA assay was performedas described previously (7).

    RESULTS

    AP-2? interacts with GAS41 in yeast two-hybrid assay

    To identify AP-2?–interacting proteins, we first performed yeast two-hybrid screening using full-length AP-2? protein as

    the bait and the HeLa cell cDNA library as a prey. The transactivational activity of the GAL4-AP-2? fusion protein in yeast

    was inhibited by 25 mM 3-AT. Approximately 2.0 x 106 transformants were screened and thirty clones were obtained on a SD-Leu

    –, Trp–, uracil–, His– medium supplemented with 25 mM 3-AT. Two clones were further shown to be positive when analyzed

    for ?-galactosidase activity using the colony lift assay. Sequence analysis revealed that one of the clones was identical to

    human GAS41 cDNA previously cloned from a glioblastoma cell line (39).

    AP-2? and GAS41 are co-immunoprecipitated in HeLa cells

    To demonstrate the possible interaction between AP-2? and GAS41 in mammalian cells, we asked whether the two proteins

    could be co-immunoprecipitated. HeLa cells were transiently transfected with expression vectors pCMV-Myc-AP-2? and pCMV-HA-

    GAS41. The lysates were immunoprecipitated with either control IgG or anti-HA polyclonal antibody. The co-immunoprecipitated

    protein was examined for the presence of Myc-AP-2? by immunoblotting assay using anti-Myc monoclonal antibody. As shown in

    Figure 1A, AP-2? could be co-immunoprecipitated with HA tagged GAS41 (Figure 1A, lane 2) but not by control rabbit IgG

    (Figure 1A, lane 3). To further confirm this finding, the same lysates were immunoprecipitated with anti-Myc monoclonal

    antibody, and the bound protein was detected by immunoblotting with anti-HA polyclonal antibody. As shown in Figure 1B, GAS41

    could also be precipitated by Myc tagged AP-2? (Figure 1B, lane 2) but not by control mouse IgG (Figure 1B, lane 3).

    Furthermore, HeLa cells were only transfected with pCMV-Myc-AP-2?. Endogenous GAS41 in HeLa cells could be co-

    immunoprecipitated with Myc tagged AP-2? (Figure 1C, lane 2) but not by control mouse IgG (Figure 1C, lane 3). These results

    indicated that AP-2? and GAS41 could be found in the same complex in mammalian cells, and GAS41 may directly or indirectly

    interact with AP-2?.

    AP-2? colocalizes with GAS41 in HeLa cell nuclei

    Because of the tight association found in immunoprecipitation experiments, we next investigated whether these proteins

    were present in the same region in cells. The immunofluorescent assays were performed as described in Materials and Methods.

    The images obtained with confocal laser scanning microscope revealed that both Myc-tagged AP-2? (Figure 2B) and HA-tagged

    GAS41 (Figure 2C) were localized in the nuclei of cells. After overlay, co-localized signals (yellow) were clearly observed

    (Figure 2D). These results are consistent with the presence of GAS41 and AP-2? in same complex in vivo but do not address

    whether both proteins directly interact.

    AP-2? and GAS41 interact directly in vitro

    It is possible that GAS41-AP-2? interaction may be indirect because other protein factors in the whole cell extract may

    be involved in mediating the interaction, e.g. acting as ‘bridging’ factors. Therefore we next decided to examine a

    possible direct interaction between the two proteins using GST pull-down assays. GST, GST fusion proteins and His fusion

    proteins were expressed and purified. Figure 3A showed the bacterially expressed and purified proteins. Figure 3B showed that

    GAS41 could be pulled-down by GST fused AP-2? (Figure 3B, lane 2) but not by GST alone (Figure 3B, lane 3), indicating that

    GAS41 and AP-2? specifically interact directly in vitro. We next decided to map the interaction domains between AP-2? and

    GAS41 using the same assay. The truncated proteins of AP-2? (Figure 3C and E) were used with His-GAS41 in pull-down

    experiments (Figure 3D and F). AP-2? P62R with the PY motif mutation that causes Char Syndrome (40) and AP-2?N233 efficiently

    pulled down GAS41 (Figure 3D and F, lanes 4 and 5), whereas other truncations of AP-2? pulled down little or none of GAS41

    ((Figure 3D and F). The results obtained indicated that domain of AP-2? interacting with GAS41 is located in the C-terminus.

    The domain of GAS41 interacting with AP-2? was also mapped by same assay. As shown in Figure 4A, GST-AP-2? pulled down

    His-GAS41N162 (Figure 4A, lane 4), but not His-GAS41C96 (Figure 4A, lane 2). The His-GAS41N162 contains C-terminal 65 amino

    acid residues (amino acids 163–227) of GAS41, indicating that the domain of GAS41 interacting with AP-2? is located in C-

    terminus. We next examined the ability of different fragments of GAS41 to interact with AP-2?. A further C-terminal deletion

    that deleted residues 215–227 did not affect the interaction with AP-2? (Figure 4B, lane 7). But deletions of C-terminal

    residues 203–227 and 193–227 abrogated the interaction (Figure 4B, lanes 8 and 9). And the further deletion of the C-

    terminal residues 212–227 and 208–227 also affected the interaction (Figure 4C, lanes 6–9). These results suggest lysine

    at position 212, Asparagine at position 213, Glutamic acid at position 214 or three are possibly critical for the

    interaction. Moreover, the three point mutations of GAS41, respectively, significantly reduced the interaction with AP-2?

    confirmed by the GST pull-down assay (Figure 4D) and co-immunoprecipitation (Figure 4E). However, GAS41 containing the three

    point mutations did not interact with AP-2?, (Figure 4E, lane 2). Therefore, the three residues of GAS41 have played an

    important role in the interaction, but we haven't found any change in their co-localization (data not shown).

    GAS41 stimulates activation of transcription by AP-2?

    To investigate the physiological relevance of the AP-2?-GAS41 interaction, we asked whether GAS41 could modulate AP-2?

    transcriptional activity. The A2-luc reporter construct was transfected into HepG2 cells either alone or together with AP-2?

    expression vector pCMV-Myc-AP-2? and/or GAS41 expression vector pCMV-HA-GAS41 as well as the mutants of GAS41 as indicated in

    the Figure 5. GAS41 alone hardly stimulated the luciferase expression (Figure 5, lane 2) in HepG2 cells which lack the

    expression of AP-2 proteins. Transfection of AP-2? significantly stimulated the luciferase activity (Figure 5, lane 3). The

    addition of GAS41 enhanced AP-2? activity (Figure 5, lane 4). Furthermore, notably, these mutations reduced their ability in

    stimulating AP-2? activity (Figure 5, lanes 5–8). Taken together, these results suggested that GAS41 can function as co-

    activator of AP-2?.

    GAS41 enhances binding of AP-2? to DNA

    To elucidate the mechanism for the enhanced transcription activity of AP-2? by GAS41, we then examined whether GAS41

    affected the formation of AP-2?–DNA complexes by the EMSA experiment. First, we documented the DNA-binding specificity, 10-

    and 50-fold amounts of unlabeled AP-2, Sp1 or SV40 oligonucleotide were added in competition. Cold AP-2 oligonucleotide

    significantly competed away the signal, whereas cold Sp-1 or SV40 oligonucleotide did not reduce the intensity of the band

    (Figure 6A). The result documented that AP-2? binds the consensus AP-2 site with specificity.

    As shown in Figure 6B, His-GAS41 significantly enhanced the DNA-binding activity of GST-AP-2? (lanes 5–7), comparing

    with BSA (lanes 2 and 3). The stimulatory effect of His-GAS41 was dose dependent. GAS41 alone incubated with the probe did

    not produce a band (lane 4). Furthermore, the point mutants of GAS41 markedly reduced the enhancement for DNA-binding

    activity of GST-AP-2? (lanes 9–11) compared to the same amount of wild-type GAS41 (lane 7), whereas the mutant GAS41 that is

    not capable of interacting with AP-2? did not stimulate the DNA-binding activity of GST-AP-2? (lane 8). Taken together, our

    result suggests GAS41 enhances the transcriptional activity by a mechanism that appears to involve an enhancement in the

    formation of AP-2?–DNA complex.

    DISCUSSION

    We reported here the interaction between transcription factor AP-2? and GAS41, which resulted in the enhancement of

    transcriptional activity of AP-2?. The stimulating effect of GAS41 to AP-2? was, at least in part, due to the enhancement of

    AP-2? to bind to its specific DNA-binding site. In the EMSA assay, GAS41 appears to enhance the binding of AP-2? to DNA

    without affecting the rate of migration of this complex. There may be a transient interaction between GAS41 and AP-2? in

    which GAS41 induces conformational change of AP-2?, favoring its DNA-binding. After AP-2? bound to its DNA, GAS41 leaves

    without forming a ternary complex. Such ‘hit and run’ mechanism has been demonstrated for the effects of Miz 1 over the

    DNA-binding of transcription factor Msx2 (41) and oncogene DEK over AP-2 (35). In both transient transfection and EMSA

    assays, the GAS41 protein with mutation of three critical amino acid residues that does not interact with AP-2? lost its

    stimulating effect on AP-2? activity, whereas those with mutation of single amino acid residue that significantly reduced

    their abilities to interact with AP-2? also significantly reduced their stimulating activity over AP-2? (Figures 4–6),

    suggesting that the interaction between GAS41 and AP-2? is essential for the physiological relevance of these two proteins.

    To the best of our knowledge, this is the first report that suggests a role for GAS41 as a co-activator of a sequence-

    specific transcription factor by directly interacting with the transcription factor AP-2?. In addition, GAS41 also stimulated

    the transcriptional activity of endogenous AP-2 family members in COS7, MCF-7 and NIH3T3 cells (data not shown).

    GAS41 gene was originally identified as an amplified sequence in the chromosome region 12q13–15, a region known to be

    involved in gene amplification in human gliomas (39). GAS41 amplification was detected in 23% of glioblastomas and 80% of

    grade I astrocytomas, suggesting gene amplification can occur not only in late tumor progression but also in early tumor

    development (39,42). Sequence analysis and comparison of GAS41 and known protein sequences revealed a high similarity between

    GAS41 and human AF-9 and ENL proteins (43). This finding is intriguing since AF-9 and ENL genes are frequently involved in

    translocation events in leukemia, in particular, AF-9 being found fused to the ALL-gene with t(9:11) translocations and ENL

    being found fused to the ALL-1 gene with t(11:19) translocations (44), leaving the question open whether GAS41 also plays

    roles in leukemia.

    GAS41 is a highly conserved protein with homologous found in invertebrates, vertebrates, plants and fungi (43). It is

    probably one of most highly conserved proteins during evolution with the degree of homology between human and Drosophila

    proteins of 61% identity and 70% overall similarity (43), suggesting GAS41 may play an essential role during biological

    evolution. A number of proteins involved in nuclear matrix formation, chromatin remodeling, nuclear scaffolding or mitotic

    spindle assembly have been shown to interact with GAS41, those including NuMA (43), TACC1 (37) and AF10 (45). It is possible

    that by associating with those factors, GAS41 can produce a change in chromatin conformation in such a way that enhances the

    DNA-binding of transcription factor, such as AP-2? in vivo. Recent studies have also been shown that targeted disruption of

    GAS41 in chicken pre-lymphoid cells results in cell death, indicating that it is essential for cell viability. It has been

    further demonstrated that depletion of GAS41 causes a significant decrease in RNA synthesis and subsequently cell death,

    suggesting a role of GAS41 in gene transcription (46). The gene transcription in eukaryotes is a quite complicated process

    which has not been fully understood. However, the transcription of a specific gene is generally processed by: (i) remodeling

    of chromatin to facilitate the binding of subsequent factor to nucleosomal DNA, involving the participation of SWI–SNF

    complex or other homologous multiprotein complexes with similar chromatin-remodeling activities, (ii) formation of

    transcription initiation complex involving recruiting of general transcription factors (TFIIA, TFIIB, TFIID, TFIIF, etc.) and

    RNA polymerase II to the transcription initiation sites of specific gene, (iii) the interaction of sequence-specific

    transcription factors with the basal transcriptional initiation complex to enhance or repress the transcription rate. GAS41

    seems to be a mediator among these three steps. GAS41 appears to be a human homologue of yeast ANC1, a protein known to be an

    integral member of two basal transcription factor complexes, TFIID and TFIIF. ANCI binds to the SWI–SNF chromatin-remodeling

    complex through its interaction with SNF5, a component of SWI–SNF complex (47). Homologues of SNF5 have been isolated in

    both human and Drosophila, named INT1 and Snr1, respectively. They have been shown to be component in large complexes

    equivalent to the yeast SWI–SNF5 complex (48,49). It has been shown that GAS41 can interact with INI1 (45), which bridges

    the chromatin-remodeling complex and the basal transcription complex. As a component of basal transcription complex, GAS41

    has been proposed to regulate gene transcription by directly associating with the sequence-specific transcription factor.

    However, previous to this report, GAS41 has not been shown to bind directly to any known transcription factor. So, it is

    proposed that an additional protein may be required for GAS41 to bind to sequence-specific transcription factor. Our finding

    fulfils such gap, indicating that GAS41 can bind to DNA-sequence-specific transcription factor, such as AP-2?. It is possible

    that, as a component of basal transcription complex, one of the roles of GAS41 is to act as a recruiting protein for certain

    sequence-specific transcription factors in vivo. Taken together, it is attemptable to speculate that the general role of

    GAS41 is to function as a mediator which bridges the chromatin-remodeling complex, basal transcription complex and DNA-

    sequence-specific transcription factor to facilitate the efficient gene transcription, and deregulation of GAS41

    transcription would result in diseases, such as gliomas and leukemia.

    ACKNOWLEDGEMENTS

    The authors are grateful to Mr Yunhai Liu for cell culture, Dr T. Williams and members of Zhang's lab for critical

    reading of the manuscript and helpful discussion. This work was supported in part by the National Natural Science Foundation

    of China (Nos 20335020, 30470945), the Program for Changjiang Scholars and Innovative Research Team in University (No.

    IRT0445), the 973 project of Ministry of Science and Technique of China (No. 2005CB522505), the Cultivation Fund of the Key

    Scientific and Technical Innovation Project, Ministry of Education of China (No. 705041), and The E-Institutes of Shanghai

    Municipal Education Commission (No. E03003 [GenBank] ). Funding to pay the Open Access publication charges for this article

    was provided by IRT0445.

    Conflict of interest statement. None declared.

    REFERENCES

    Williams, T., Admon, A., Luscher, B., Tjian, R. (1988) Cloning and expression of AP-2, a cell-type-specific transcription

    factor that activates inducible enhancer elements Genes Dev, . 2, 1557–1569.

    Moser, M., Imhof, A., Pscherer, A., Bauer, R., Amselgruber, W., Sinowatz, F., Hofstadter, F., Schule, R., Buettner, R.

    (1995) Cloning and characterization of a second AP-2 transcription factor: AP-2 beta Development, 121, 2779–2788

    Bosher, J.M., Totty, N.F., Hsuan, J.J., Williams, T., Hurst, H.C. (1996) A family of AP-2 proteins regulates c-erbB-2

    expression in mammary carcinoma Oncogene, 13, 1701–1707.

    Zhao, F., Lufkin, T., Gelb, B.D. (2003) Expression of Tfap2d, the gene encoding the transcription factor Ap-2 delta,

    during mouse embryogenesis Gene Expr. Patterns, 3, 213–217.

    Wang, H.V., Vaupel, K., Buettner, R., Bosserhoff, A.K., Moser, M. (2004) Identification and embryonic expression of a new

    AP-2 transcription factor, AP-2 epsilon Dev. Dyn, . 231, 128–135.

    Feng, W. and Williams, T. (2003) Cloning and characterization of the mouse AP-2 epsilon gene: a novel family member

    expressed in the developing olfactory bulb Mol. Cell. Neurosci, . 24, 460–475 .

    Williams, T. and Tjian, R. (1991) Analysis of the DNA-binding and activation properties of the human transcription factor

    AP-2 Genes Dev, . 5, 670–682.

    Williams, T. and Tjian, R. (1991) Characterization of a dimerization motif in AP-2 and its function in heterologous DNA-

    binding proteins Science, 251, 1067–1071.

    Somasundaram, K., Jayaraman, G., Williams, T., Moran, E., Frisch, S., Thimmapaya, B. (1996) Repression of a matrix

    metalloprotease gene by E1A correlates with its ability to bind to cell type-specific transcription factor AP-2 Proc. Natl

    Acad. Sci. USA, 93, 3088–3093.

    Bosher, J.M., Williams, T., Hurst, H.C. (1995) The developmentally regulated transcription factor AP-2 is involved in c-

    erbB-2 overexpression in human mammary carcinoma Proc. Natl Acad. Sci. USA, 92, 744–747 .

    Gaubatz, S., Imhof, A., Dosch, R., Werner, O., Mitchell, P., Buettner, R., Eilers, M. (1995) Transcriptional activation

    by Myc is under negative control by the transcription factor AP-2 EMBO J, . 14, 1508–1519.

    McPherson, L.A., Baichwal, V.R., Weigel, R.J. (1997) Identification of ERF-1 as a member of the AP2 transcription factor

    family Proc. Natl Acad. Sci. USA, 94, 4342–4347.

    Zeng, Y.X., Somasundaram, K., el-Deiry, W.S. (1997) AP2 inhibits cancer cell growth and activates p21WAF1/CIP1 expression

    Nature Genet, . 15, 78–82

    Zhao, F., Weismann, C.G., Satoda, M., Pierpont, M.E.M., Sweeney, E., Thompson, E.M., Gelb, B.D. (2001) Novel TFAP2B

    mutations that cause char syndrome provide a genotype-phenotype correlation Am. J. Hum. Genet, . 69, 695–703

    Wu, L., Wu, H., Ma, L., Sangiorgi, F., Wu, N., Bell, J.R., Lyons, G.E., Maxson, R. (1997) Miz1, a novel zinc finger

    transcription factor that interacts with Msx2 and enhances its affinity for DNA Mech. Dev, . 65, 3–17

    Fischer, U., Heckel, D., Michel, A., Janka, M., Hulsebos, T., Meese, E. (1997) Cloning of a novel transcription factor-

    like gene amplified in human glioma including astrocytoma grade I Hum. Mol. Genet, . 6, 1817–1822 .

    Harborth, J., Weber, K., Osborn, M. (2000) GAS41, a highly conserved protein in eukaryotic nuclei, binds to NuMA J. Biol.

    Chem, . 275, 31979–31985

    Nakamura, T., Alder, H., Gu, Y., Prasad, R., Canaani, O., Kamada, N., Gale, R.P., Lange, B., Crist, W.M., Nowell, P.C.,

    et al. (1993) Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology

    and/or common motifs Proc. Natl Acad. Sci. USA, 90, 4631–4635

    Debernardi, S., Bassini, A., Jones, L.K., Chaplin, T., Linder, B., de Bruijn, D.R., Meese, E., Young, B.D. (2002) The MLL

    fusion partner AF10 binds GAS41, a protein that interacts with the human SWI/SNF complex Blood, 99, 275–281

    Zimmermann, K., Ahrens, K., Matthes, S., Buerstedde, J.M., Stratling, W.H., Phi-van, L. (2002) Targeted disruption of the

    GAS41 gene encoding a putative transcription factor indicates that GAS41 is essential for cell viability J. Biol. Chem, .

    277, 18626–18631

    Cairns, B.R., Henry, N.L., Kornberg, R.D. (1996) TFG/TAF30/ANC1, a component of the yeast SWI/SNF complex that is similar

    to the leukemogenic proteins ENL and AF-9 Mol. Cell. Biol, . 16, 3308–3316

    Wang, W., Cote, J., Xue, Y., Zhou, S., Muchardt, C., Khavari, P.A., Biggar, S.R., Kalpana, G.V., Goff, S.P., Yaniv, M.,

    et al. (1996) Purification and biochemical heterogeneity of the mammalian SWI-SNF complex EMBO J, . 15, 5370–5382

    Dingwall, A.K., Beek, S.J., McCallum, C.M., Tamkun, J.W., Kalpana, G.V., Goff, S.P., Scott, M.P. (1995) The Drosophila

    snr1 and brm proteins are related to yeast SWI/SNF proteins and are components of a large protein complex Mol. Biol. Cell, 6,

    777–791(Xiaofeng Ding1, Changzhen)