Bright/ARID3A contributes to chromatin accessibility of the immunoglobulin heavy chain enhancer
© Lin et al; licensee BioMed Central Ltd. 2007
Received: 12 February 2007
Accepted: 26 March 2007
Published: 26 March 2007
Bright/ARID3A is a nuclear matrix-associated transcription factor that stimulates immunoglobulin heavy chain (IgH) expression and Cyclin E1/E2F-dependent cell cycle progression. Bright positively activates IgH transcriptional initiation by binding to ATC-rich P sites within nuclear matrix attachment regions (MARs) flanking the IgH intronic enhancer (Eμ). Over-expression of Bright in cultured B cells was shown to correlate with DNase hypersensitivity of Eμ. We report here further efforts to analyze Bright-mediated Eμ enhancer activation within the physiological constraints of chromatin. A system was established in which VH promoter-driven in vitro transcription on chromatin- reconstituted templates was responsive to Eμ. Bright assisted in blocking the general repression caused by nucleosome assembly but was incapable of stimulating transcription from prebound nucleosome arrays. In vitro transcriptional derepression by Bright was enhanced on templates in which Eμ is flanked by MARs and was inhibited by competition with high affinity Bright binding (P2) sites. DNase hypersensitivity of chromatin-reconstituted Eμ was increased when prepackaged with B cell nuclear extract supplemented with Bright. These results identify Bright as a contributor to accessibility of the IgH enhancer.
Numerous studies have demonstrated the requirement of the intronic enhancer (Eμ) in transcription of immunoglobulin heavy chains (reviewed in ). In vivo, Eμ is required for successful B-cell development, and in its absence, completion of antigen receptor assembly through VDJ recombination is blocked [2, 3]. Based on chromatin immunoprecipitation (ChIP) measurements of its histone modification status, Eμ assumes an accessible chromatin configuration specifically in B cells [4–6]. Conventional transcription factors may seize upon this B cell-accessible state to bind to Eμ for transactivation via VDJ-associated promoters (Fig. 1A). Transcriptional activators further exploit increasingly accessible chromatin structures to enhance their binding as B cells progress through development .
Bright, a nuclear matrix-associated, B cell-restricted r egulator of IgH t ranscription, binds with differential affinity to four ATC-rich motifs (P1–P4, Fig. 1B) within the Eμ MARs to activate transcription of IgH . Bright is stage-specifically expressed in B lymphocytes, where it accumulates primarily within the cytoplasm and the nuclear matrix [22–24]. In addition to its participation in IgH transcription, a function for Bright in cell cycle regulation was suggested by the finding that a fraction of nuclear matrix-associated Bright fractionated into PML nuclear bodies . Consistent with this notion, ectopic over-expression of Bright in embryonic fibroblasts leads to their immortalization via accumulation of Cyclin E and activation of E2F1 . Potential relevance of these observations to B-cell malignancy is suggested by the finding that the sub-type of diffuse large B-cell lymphoma with the worst clinical prognosis has elevated levels of Bright [27, 28].
Bright is the founder of the 13-member (in humans) ARID (AT-R ich I nteraction D omain) family . Bright/ARID3A and several other ARID members (or their fly or yeast orthologues) have been implicated directly or indirectly in chromatin remodeling [30–35]. As often seen with remodeling proteins, Bright has strict contextual requirements for transactivation [21, 30]. For example, Bright cannot transactivate via out-of-context, concatenated P binding sites, and transactivation is maximal on integrated substrates [21, 30]. Bright binding to its highest affinity P2 site within the Eμ 5' MAR induces severe (80–90)° bending [21, 30]. Over-expression of Bright in a mature B cell line induced DNAse I hypersensitivity extending through both Eμ MARs . These results suggest that the enhancer assumes a more open chromatin configuration as a direct or indirect consequence of Bright.
To address the issue directly, we have examined Bright transcriptional activation in an Eμ-responsive chromatin-reconstituted in vitro system. Our results support a role for Bright, or a Bright complex which retains Eμ MAR binding, in chromatin remodeling of the enhancer.
Rationale and reaction order
In vitro transcription on reassembled chromatin templates is the only in vitro system in which transcriptional enhancement over distances of 1–2 kb has been achieved (e.g., ). Activity requires that the template be packaged into chromatin and that the transcriptional regulatory factors be present before or during chromatin formation so that general repression caused by nucleosome assembly will be blocked.
The 3 template DNAs employed in this study are shown in Fig. 1C, and their construction is detailed in Methods and Materials. Transcription is driven from the promoter of the rearranged VDJ expressed by the BCL1 leukemia B cell line . VHBCL1 extends ~270 bp upstream of the 5' most transcriptional initiation site and includes the conserved heptamer and octamer binding motifs  (Fig. 1D). VHBCL1 has been shown to have strong in vitro activity when assayed in nuclear extracts [39, 40]. The Eμ core alone (Eμ) or flanked by 5' and 3' MARs (Eμ+MARs) is positioned ~2 kb downstream (or ~400 bp upstream on the circular plasmid backbone) (Fig. 1C).
Our experimental design is shown in Fig. 1E. There are two orders of addition. In the first, naked DNA templates are prebound with nuclear extract from B-cell lines, or with recombinant Bright, or with B-cell extracts supplemented with recombinant Bright (or with buffer) (Step 1). Chromatin is assembled using S-190 extracts from 4 hr Drosophlia embryos supplemented with core histones [41, 42]. Following chromatin assembly (Step 2), packaged templates are assayed upon addition of nucleotide triphosphates for transcription initiated off of the VHBCL1 promoter by quantitative RNase protection. Chromatin alterations are measured by DNase I digestion and indirect end labeling. In the second order of addition, extracts or purified Bright are added following chromatin assemblies.
The Step 1 condition will reveal direct effects on chromatin structure. In this scheme, extracts or purified Bright prebound to the naked DNA template before or during chromatin formation can derepress the general transcriptional repression of assembled nucleosomes. If an effect is seen at addition of extract or Bright at step 2, this would suggest that transcriptional activation requires binding to a pre-formed, reconstituted nucleosome array.
Assembly of chromatin on IgH templates
Transcription from in vitro assembled VH-promoter-driven templates is responsive to Eμ
Choice and production of endogenous and recombinant Bright
We reasoned that the abundance of endogenous Bright within a B cell nuclear extract would directly correlate with its transcriptional activity. As shown in the Western analysis of Fig. 4A, Bright levels varied broadly among the human B cell lines examined. We prepared standard nuclear extracts fractionated over heparin agarose from the relatively Bright-low (Namalwa, lane 8) and Bright-high (Nalm6, lane 4) cell lines.
Next, we sought to purify recombinant Bright to replace or to complement extracts for reaction Steps 1 and 2. Several methods to produce full-length Bright (1–601) in E. coli were attempted, but these attempts were unsuccessful in producing functional protein (data not shown). The material remained insoluble and could not be actively (as judged by EMSA; data not shown) renatured from inclusion bodies. However, we produced sufficient quantities of an N-terminally His-tagged truncation (residues 177–601). This same truncation was previously shown to be indistinguishable from wild-type as an Eμ transactivator in transfected B cell lines . As judged by SDS-PAGE chromatography (Fig. 4B, left panel), Bright (177–601) was purified to near homogeneity by a combination of affinity and ion exchange chromatography. The faster migrating species was confirmed by Western analysis (data not shown) as a Bright degradation product. This degradation was prevented/significantly reduced (Fig. 4B, left panel, lane 5) by transformation into a chaperone over-expressing E. coli strain .
Bright stimulates in vitro transcription by relieving the inhibitory effect of chromatin
Summary of in vitro transcription results of Figures 4, 5 and data not shown.
Enhancer derepression by Bright requires P site-specific MAR binding
Bright levels correlate with increased enhancer accessibility
Numerous ubiquitous and B cell-specific transcription factors have been identified that transactivate the IgH enhancer (Fig. 1B; reviewed in ). Functional analyses underlying most characterizations have relied on transient reporter assays and have ignored to a large extent the physiological role of chromatin. Chromatin imposes an obligatory negative constraint upon enhancer accessibility. Thus, while conclusions derived from reporter approaches are valid in the context of accessible regulatory elements, they do not address many basic mechanisms of enhancer activation.
The concept of locus accessibility is at the heart of antigen receptor VDJ and class switch recombination (reviewed in ). However, few bonafide accessibility factors have been identified. Perhaps the best characterized Eμ accessibility factor is the ETS transcription factor family member, PU.1 [46, 47]. PU.1 functions through the interaction with another ETS protein, Ets-1, to transactivate Eμ and to stimulate enhancer accessibility in cultured cells via μB site binding (Fig. 1B) [48, 49]. Importantly, PU.1 was observed to stimulate in vitro transcription and Eμ accessibility from chromatin reconstituted templates . In contrast, another essential Eμ-binding transactivator, E47, appears to function indirectly by weak binding to accessible μE5/μE2 sites (Fig. 1B) [51, 52].
We previously showed that Bright/ARID3A, when over-expressed in cultured WEHI 231 B cells, facilitated DNase I hypersensitivity of Eμ . Four other members of the 13 member ARID family (including SWI1/p270 of SWI/SNF) have been directly or indirectly implicated in chromatin remodeling [31–35]. Prompted by these observations, we established a system in which transcription from in vitro assembled VH-promoter-driven templates was responsive to Eμ. We found that Bright could complement other B cell-derived factors to derepress the inhibitory effects of chromatin assembled on the enhancer. The Eμ flanking MARs were required for maximal Bright-mediated in vitro transactivation. We demonstrated that the DNase I hypersensitivity of chromatin assembled in vitro on the enhancer was increased by Bright. These data indicate a direct role for Bright and further support a role for the Eμ MARs in facilitating a fully accessible chromatin state of Eμ.
Our previous analysis  and unpublished MNase digestion experiments on isolated B cell nuclei suggested that Bright may function by Eμ nucleosomal disruption. The simplest mechanism to explain this effect would require that Bright reach the enhancer in the context of heterochromatin. However, the results reported here showed that Bright could alleviate chromatin-mediated repression only if it was delivered prior to chromatin assembly. That is, Bright cannot activate in vitro transcription by binding to a preformed nucleosome array. In contrast, in vitro assembled chromatin footprinting experiments revealed that PU.1 is capable of binding μB in the repressive context of chromatin . The authors speculated that PU.1 might provide a platform for assembly of a "targesome", a protein complex required for a fully accessible chromatin structure . Bright might participate in such a complex. However, as with PU.1 , our competition experiments indicated that Bright required an intact DNA binding site to mediate maximal Eμ chromatin accessibility. This suggests that Bright is recruited independently and perhaps subsequently to PU.1, through direct binding to its P site(s). Both PU.1 and Bright might function to clear out nucleosomes otherwise positioned over critical cis-acting regulatory elements within the Eμ core to provide accessibility to conventional DNA-binding transactivators.
Regulation of chromatin structure by conventional protein-DNA interactions is generally considered to act only proximal to the DNA binding site [54, 55]. MARs might offer an exception to this case. Forrester et al [16, 56] demonstrated that the Eμ MARs were required to obtain normal transcription initiation rates and to produce extended DNase I hypersensitivity across a VDJ-associated promoter over 2 kbp away. The mechanism underlying such distal accessibility induction is unknown, but it seems reasonable to speculate that a MAR-binding accessibility factor might contribute. As mentioned in the Background section, the contradictory evidence on Eμ MAR function rests to a large extent on whether the endogenous locus or a transgenic locus was investigated [3, 18–20, 34–36, 57]. For example, studies using chimeric mice with targeted deletion of the Eμ MARs reported that these elements were dispensable for VDJ recombination and transcription of the endogenous IgH locus . However, while the endogenous and MAR-deleted alleles were expressed at similar levels in splenic IgM+ B cells , the total numbers of IgM+ B cells in mice with a MAR deletion were less than half of those observed in wild-type mice or mice with deletion of only the Eμ core. This suggests that deletions of the MAR elements may result in defects in B-cell development that have yet to be fully appreciated. The requirement for MAR function in transgenic animals, but not in cell lines or animals created from blastocyst fusions, is consistent with a MAR function in chromatin remodeling during early development or passage through the germline. This is consistent with the results of Forrester et al.  and those presented here.
In addition to Eμ, IgH-associated MARs often reside 5' of VH promoters [58–60]. A MAR upstream of the S107 variable region VH1 promoter was shown to contain specific Bright-binding P sites . Indeed, Webb and colleagues have convincingly demonstrated that Bright can associate with both Bruton's tyrosine kinase and TFII-I to activate transcription of a S107 VH1 reporter through this proximal MAR in the absence of Eμ [61, 62]. The existence of VH and Eμ-associated MARs and the ability of Bright to form multimeric MAR binding complexes  offers the possibility of looping enhancers and promoters into close proximity to stimulate transcription through nuclear matrix attachment-mediated domain formation . Whether the in vivo mechanisms underlying promoter-proximal (VH) and promoter-distal (Eμ) MAR-mediated transactivation by Bright are the same and can be accommodated by the looping model remain to be tested. In this context, we note that Bright levels in adult mice spike distinctly in large preB and mature B cells . At the latter stage, maximal Bright expression and VH1 DNA binding are induced by mitogens and cytokines (e.g., LPS, IL-5, CD40L) that drive B lymphocytes into the cell cycle [21, 22]. Perhaps Bright might utilize quite different transactivation options and/or function through different IgH MAR-associated binding sites under circumstances in which accessibility of Eμ has already been established.
Finally, we suggest that Bright may contribute to chromatin remodeling at loci other than IgH. Bright was shown to rescue primary fibroblasts from natural replicative senescence or from premature senescence induced by oncogenic RASV12 . As with several other ARID factors [31, 63], Bright binds retinoblastoma protein (Rb) (C. Schmidt and PWT, unpublished results), leading to the possibility that this tumour suppressor pathway is inactivated during senescence rescue. This hypothesis is consistent with the observation that Bright over-expression in MEFs activates E2F1 and Cyclin E1 . Dean and colleagues  have provided a chromatin-based explanation for Rb/E2F transcriptional regulation which could accommodate a contributor with the properties of Bright.
We established a chromatin-reconstituted, in vitro transcription system which is responsive to the IgH enhancer. Our results support the conclusion that Bright contributes to enhancer function by increasing its accessibility through matrix attachment site binding.
Materials and methods
Constructs, probes and oligonucleotides
The template plasmids for in vitro transcription were constructed by cloning the 593 bp BamH1-XbaI fragment that spans the rearranged VDJ expressed by the BCL1 leukemia cell line  into pUC19. This fragment (VHBCL1) contains ~270 bp upstream of the 5' most transcriptional initiation site, including the conserved heptamer and octamer binding motifs . VHBCL1- Eμ was constructed by inserting the Eμ enhancer core, as a 220 bp HinfI fragment, ~2 kbp downstream in transcriptional sense (~400 bp upstream on circular plasmid) of VHBCL1. VHBCL1-Eμ+MARs was constructed by inserting Eμ along with its flanking 5' and 3'MARs as a 911 bp Xba I fragment into the same location relative to VHBCL1. For the VHBCL1 antisense RNase protection probe, a 322 bp BamH1-NruI fragment containing ~55 bp downstream from the major initiation of transcription site was cloned into pGEM4 to generate pBCL1-5'. The plasmid was linearized with HinfI and transcribed in vitro by sp6 polymerase (Promega) to generate a 95 b RNA probe. Oligonucleotides corresponding to the + and - strands of wild-type (5'-CTTTTAACAATAATAAATTAA GTTTAAAATATTTTT-3') or mutated (underlined bases changed to TAATT) P2 Bright binding site within the Eμ 5' MAR were synthesized, annealed, and the resulting duplex was gel purified as previously described .
The BCL1 murine leukemia, and human Burkitt's lymphomas (BJAB, Nalm6 and Namalwa) were maintained in RPMI supplemented with 10% fetal calf serum. For protein purification, we employed either E. coli BL21 Star (Invitrogen) or E coli K1309 , a strain overproducing chaperones groE and groF kindly provided by Dr. G. Georgiou (UT Austin, Dept. of Chem. Engineering). Induction of the chaperones was induced with 10 ng/ml-1 tetracycline at the beginning of the incubation in LB or M9 media.
Labeling, purification, and denaturating gel analysis of the pBCL1-5' riboprobe were carried out as previously described . After hybridization at 60°C overnight, unduplexed probe was digested with 40 ug RNase A (Sigma)/ml and 2500 U RNase T1 (BRL) for 1 hr at 37°C. Protected RNA fragments were separated on 6% acrylamide gels containing 8 M urea, and autoradiography was carried out for 24–96 hr.
An N-terminal 6X-histidine-tagged Bright truncation (amino acids 177–601) was constructed as previously described , cloned into the pET30a+ expression vector (Novagen), and its expression induced with IPTG 30 min after chaperone induction (see above). Harvested cells were disrupted by sonication, and total cell lysates were analyzed on 12% SDS-PAGE (prior to or as a monitor of purification) with SilverStain (Invitrogen). Following elimination of cell debris by centrifugation, supernatants were purified by affinity chromatography over Ni2+-NTA agarose SuperFlow according to the manufacturer's instructions (Novagen and Qiagen). Further purification was carried out by DEAE Bio-Gel agarose chromatography as instructed by the vender (Pharmacia Fine Chemicals). The Bright-containing fraction was subjected to DNA affinity chromatography employing a Sepharose 6B-conjugated, high affinity Bright binding P2 site trimer (synthesis and elution conditions as described ). The final yield of purified Bright (177–601) was 8–20 μg from 2 l of M9 or LB media, respectively.
Western analysis was performed according to Kim and Tucker . Proteins were separated by 9% SDS-PAGE and transferred to Protran nitrocellulose membranes (Perkin Elmer). The membranes were incubated with anti-Bright polyclonal  and then developed with goat anti-rabbit IgG peroxidase-conjugated secondary (Amersham). Bands were visualized with ECL Western Blotting Detection Reagents (Amersham).
Electrophoretic mobility shift assays (EMSA)
In vitro DNA binding and antibody supershift reactions were performed as previously described [21, 66]. Briefly, either ~2 μg of nuclear extract or ~20 ng of purified Bright (177–601) was incubated with ~80,000 cpm of 5' end-labeled and gel-purified Bright-specific 5' Eμ MAR probe (Fig. 1B). Samples were incubated for 20 min at room temperature and then resolved on 4% polyacrylamide gels.
Chromatin reconstitution and in vitro transcription
Chromatin was assembled onto circular plasmid DNA templates using Drosophila core histones and S-190 assembly extract, derived from Drosophila embryos as previously described [41, 42]. Briefly, template DNA (~500 ng), core histones (~400 ng), S-190 (~3.0 μg), 3 mM ATP plus an ATP regenerating system (30 mM phosphocreatine and 1 μg phosphocreatine kinase/ml) were incubated in 60 mM KCl. To monitor assembly, aliquots (~100 ng DNA) were removed at regular 2–240 min intervals, and then digested with micrococcal nuclease (MNase) (0.4 units/ml) for 5 min in a 30 mM CaCl2-containing, 10 mM Hepes (pH 7.5) buffer supplemented as previously described . Reactions were deproteinized by protein K digestion, extracted with phenol/chloroform, ethanol precipitated, fractionated on a 1.5% agarose gel, and then visualized by ethidium bromide staining. Optimal assembly was achieved at ~1:.7 ratio of core histones: DNA.
In vitro transcription was carried out as described [41, 42] on ~50 ng naked or chromatin reassembled VHBCL1, VHBCL1-Eμ or VHBCL1-Eμ+MARs templates. Transcription was initiated by addition of 10 mM nucleoside triphosphates (NTPs). Complementation experiments were carried out by addition of B cell nuclear extracts (~5 μg/reaction) and/or purified Bright (177–601) (~20 ng/reaction). Variable orders of reaction were described in Results.
Chromatin accessibility measurements
DNase I digestion analysis of reconstituted chromatin templates was performed as described . Aliquots (~100 ng DNA) were digested with DNase I (Worthington; 75 μg/ml) for various times at room temperature, purified by proteinase K digestion, phenol/chloroform/isoamyl alcohol (25:24:1) extraction and ethanol precipitation. Digests were restricted with Bgl II, fractionated on a 1.4% agarose gel containing 40 mM Tris acetate and 1 mM EDTA. The DNA was blotted overnight (Bio-Rad Zeta probe), neutralized, baked under vacuo, and then prehybridized for 2 hr overnight in 0.3 M NaCl, 15 mM sodium phosphate (pH 7.0), 1.5 mM EDTA, 0.5% BLOTTO dried milk powder, 1% SDS, and 500 μg/ml sonicated herring testis DNA. The blot was hybridized overnight in the same buffer to an ~300 bp Xba I-Eco RI restriction fragment (downstream to the Eμ 3' MAR; Fig. 1B) radiolabeled to a specific activity of ~109 cpm/μg (~2.5 × 107 cpm) with a DNA labeling kit (Ambion). The sizes of hypersensitive fragments were estimated from linear fit of log DNA size vs mobility relative to DNA standards.
We thank Chhaya Das and Maya Ghosh for excellent technical assistance. We are grateful to Dr. James Kadonga for helpful discussions and generous sharing of reagents. We thank Dr. Daniel Peeper for Bright retroviral transduced fibroblasts, Paul Das for help with preparation of the manuscript, and members of our laboratory for critical comments. The work was supported by NIH grants 1F32CA110624-01A1 (GCI) and CA31534 (PWT) and the Marie Betzner Morrow endowment to PWT.
- Chowdhury D, Sen R: Regulation of immunoglobulin mu heavy chain gene rearrangements. Immunol Rev. 2004, 200: 182-186. 10.1111/j.0105-2896.2004.00177.xView ArticlePubMedGoogle Scholar
- Perlot T, Alt FW, Bassing CH, Suh H, Pinaud E: Elucidation of IgH intronic enhancer functions via germ-line deletion. Proc Natl Acad Sci USA. 2005, 102: 14362-14367. 10.1073/pnas.0507090102PubMed CentralView ArticlePubMedGoogle Scholar
- Sakai E, Bottaro A, Davidson L, Sleckman BP, Alt FW: Recombination and transcription of the endogenous Ig heavy chain locus is effected by the Ig heavy chain intronic enhancer core region in the absence of the matrix attachment regions. Proc Natl Acad Sci USA. 1999, 96: 1526-1531. 10.1073/pnas.96.4.1526PubMed CentralView ArticlePubMedGoogle Scholar
- Chowdhury D, Sen R: Stepwise activation of the immunoglobulin mu heavy chain gene locus for recombination. EMBO J. 2001, 20: 6394-6403. 10.1093/emboj/20.22.6394PubMed CentralView ArticlePubMedGoogle Scholar
- McCarthy KM, McDevit D, Andreucci A, Reeves R, Nikolajczyk BS: HMGA1 co-activates transcription in B cells through indirect association with DNA. J Biol Chem. 2003, 278: 42106-42114. 10.1074/jbc.M308586200View ArticlePubMedGoogle Scholar
- Morshead KB, Ciccone DN, Taverna SD, Allis CD, Oettinger MA: Antigen receptor loci poised for V(D)J rearrangement are broadly associated with BRG1 and flanked by peaks of histone H3 dimethylated at lysine 4. Proc Natl Acad Sci USA. 2003, 100: 11577-11582. 10.1073/pnas.1932643100PubMed CentralView ArticlePubMedGoogle Scholar
- McDevit DC, Perkins ML, Atchison ML, Nikolajczyk BS: The Ig kappa 3' enhancer is activated by gradients of chromatin accessibility and protein association. J Immunol. 2005, 174: 2834-2842.View ArticlePubMedGoogle Scholar
- Cockerill PN, Yuen MH, Garrard WT: The enhancer of the immunoglobulin heavy chain locus is flanked by presumptive chromosomal loop anchorage elements. J Biol Chem. 1987, 262: 5394-5397.PubMedGoogle Scholar
- Scheuermann RH, Garrard WT: MARs of antigen receptor and co-receptor genes. Crit Rev Eukaryot Gene Expr. 1999, 9: 295-310.View ArticlePubMedGoogle Scholar
- Cockerill PN: Nuclear matrix attachment occurs in several regions of the IgH locus. Nucleic Acids Res. 1990, 18: 2643-2648. 10.1093/nar/18.9.2643PubMed CentralView ArticlePubMedGoogle Scholar
- Imler JL, Lemaire C, Wasylyk C, Wasylyk B: Negative regulation contributes to tissue specificity of the immunoglobulin heavy-chain enhancer. Mol Cell Biol. 1987, 7: 2558-2567.PubMed CentralView ArticlePubMedGoogle Scholar
- Scheuermann RH, Chen U: A developmental-specific factor binds to suppressor sites flanking the immunoglobulin heavy-chain enhancer. Genes Dev. 1989, 3: 1255-1266.View ArticlePubMedGoogle Scholar
- Fernandez LA, Winkler M, Grosschedl R: Matrix attachment region-dependent function of the immunoglobulin mu enhancer involves histone acetylation at a distance without changes in enhancer occupancy. Mol Cell Bio. 2001, 21: 196-208. 10.1128/MCB.21.1.196-208.2001.View ArticleGoogle Scholar
- Fernandez LA, Winkler M, Forrester W, Jenuwein J, Grosschedl R: Nuclear matrix attachment regions confer long-range function upon the immunoglobulin μ enhancer. Cold Spring Harbor Symposia on Quantitative Biology. 1998, 63: 515-524. 10.1101/sqb.1998.63.515View ArticlePubMedGoogle Scholar
- Jenuwein T, Forrester WC, Qiu R-G, Grosschedl R: The immunoglobulin μ enhancer core establishes local factor access in nuclear chromatin independent of transcriptional stimulation. Genes & Dev. 1993, 7: 2016-2032.View ArticleGoogle Scholar
- Forrester WC, van Genderen C, Jenuwein T, Grosschedl R: Dependence of enhancer-mediated transcription of the immunoglobulin μ gene on nuclear matrix attachment regions. Science. 1994, 265: 1221-1225. 10.1126/science.8066460View ArticlePubMedGoogle Scholar
- Jenuwein T, Forrester WC, Fernandez-Herrero LA, Liable G, Dill M, Grosschedl R: Extension of chromatin accessibility by nuclear matrix attachment regions. Nature. 1997, 385: 269-272. 10.1038/385269a0View ArticlePubMedGoogle Scholar
- Wiersma EJ, Ronai D, Berru M, Tsui FWL, Shulman MJ: Role of the intronic elements in the endogenous immunoglobulin heavy chain locus – Either the matrix attachment regions or the core enhancer is sufficient to maintain expression. J Biol Chem. 1999, 274: 4858-4862. 10.1074/jbc.274.8.4858View ArticlePubMedGoogle Scholar
- Serwe M, Sablitzky F: V(D)J recombination in B cells is impaired but not blocked by targeted deletion of the immunoglobulin heavy chain intron enhancer. EMBO J. 1993, 12: 2321-2327.PubMed CentralPubMedGoogle Scholar
- Fernex C, Capone M, Ferrier P: The V(D)J recombinational and transcriptional activities of the immunoglobulin heavy-chain intronic enhancer can be mediated through distinct protein-binding sites in a transgenic substrate. Mol Cel Biol. 1995, 15: 3217-3226.View ArticleGoogle Scholar
- Herrscher RF, Kaplan MH, Lelsz DL, Das C, Scheuermann RH, Tucker PW: The immunoglobulin heavy-chain matrix-associating regions are bound by Bright: a B cell-specific trans-activator that describes a new DNA-binding protein family. Genes Dev. 1995, 9: 3067-3082.View ArticlePubMedGoogle Scholar
- Webb CF, Smith EA, Medina KL, Buchanan KL, Smithson G, Dou S: Expression of bright at two distinct stages of B lymphocyte development. J Immunol. 1998, 160: 4747-4754.PubMedGoogle Scholar
- Webb C, Zong RT, Lin D, Wang Z, Kaplan M, Paulin Y, Smith E, Probst L, Bryant J, Goldstein A, Scheuermann R, Tucker P: Differential regulation of immunoglobulin gene transcription via nuclear matrix-associated regions. Cold Spring Harbor Symp Quant Biol. 1999, 64: 109-118. 10.1101/sqb.1999.64.109View ArticlePubMedGoogle Scholar
- Kim D, Tucker PW: A regulated nucleocytoplasmic shuttle contributes to Bright's function as a transcriptional activator of immunoglobulin genes. Mol Cell Biol. 2006, 26: 2187-2201. 10.1128/MCB.26.6.2187-2201.2006PubMed CentralView ArticlePubMedGoogle Scholar
- Zong R-T, Das C, Tucker PW: Regulation of MAR-Dependent, Lymphocyte-Restricted Transcription through Differential Localization within PML Nuclear Bodies. EMBO J. 2002, 19: 1-11.Google Scholar
- Peeper DS, Shvarts A, Brummelkamp T, Douma S, Koh EY, Daley GQ, Bernards RA: Functional screen identifies hDRIL1 as an oncogene that rescues RAS-induced senescence. Nat Cell Biol. 2002, 4: 48-153. 10.1038/ncb742.View ArticleGoogle Scholar
- Alizadeh AA, Eisen MB, Davis RE, Ma C, Lossos IS, Rosenwald A, Boldrick JC, Sabet H, Tran T, Yu X, Powell JI, Yang L, Marti GE, Moore T, Hudson J, Lu L, Lewis DB, Tibshirani R, Sherlock G, Chan WC, Greiner TC, Weisenburger DD, Armitage JO, Warnke R, Levy R, Wilson W, Grever MR, Byrd JC, Botstein D, Brown PO, Staudt LM: Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling. Nature. 2000, 403: 503-511. 10.1038/35000501View ArticlePubMedGoogle Scholar
- Rosenwald A, Wright G, Leroy K, Yu X, Gaulard P, Gascoyne RD, Chan WC, Zhao T, Haioun C, Greiner TC, Weisenburger DD, Lynch JC, Vose J, Armitage JO, Smeland EB, Kvaloy S, Holte H, Delabie J, Campo E, Montserrat E, Lopez-Guillermo A, Ott G, Muller-Hermelink HK, Connors JM, Braziel R, Grogan TM, Fisher RI, Miller TP, LeBlanc M, Chiorazzi M, Zhao H, Yang L, Powell J, Wilson WH, Jaffe ES, Simon R, Klausner RD, Staudt LM: Molecular diagnosis of primary mediastinal B cell lymphoma identifies a clinically favorable subgroup of diffuse large B cell lymphoma related to Hodgkin lymphoma. J Exp Med. 2003, 198: 851-862. 10.1084/jem.20031074PubMed CentralView ArticlePubMedGoogle Scholar
- Wilsker D, Probst L, Wain HM, Maltais L, Tucker PW, Moran E: Nomenclature of the ARID family of DNA-binding proteins. Genomics. 2005, 86: 242-251. 10.1016/j.ygeno.2005.03.013View ArticlePubMedGoogle Scholar
- Kaplan MH, Zong R-T, Herrscher RF, Scheuermann RH, Tucker PW: Transcriptional Activation by a MAR Binding Protein: Contextual Requirements for the Function of Bright. J Biol Chem. 2001, 276: 6-16.Google Scholar
- Lia A, Kennedy BK, Barbie DA, Bertos NR, Yang XJ, Theberge MC, Tsai SC, Seto E, Zhang Y, Kuzmichev A, Lane WS, Reinberg D, Harlow E, Branton PE: RBPI recruits the mSIN3-histone deacetylase complex to the pocket of retinoblastoma tumor suppressor family proteins found in limited discrete regions of the nucleus at growth arrest. Mol Cell Biol. 2001, 21: 2918-2932. 10.1128/MCB.21.8.2918-2932.2001View ArticleGoogle Scholar
- Lia A, Lee JM, Yang WM, DeCaprio JA, Kaelin WG, Seto E, Branton PE: RBPI recruits both histone deacetylase-dependent and independent repression activities to reinoblastoma family proteins. Mol Cell Biol. 1999, 19: 6632-6641.Google Scholar
- Clissold PM, Ponting CP: JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2beta. Trends Biochem Sci. 2001, 26: 7-9. 10.1016/S0968-0004(00)01700-XView ArticlePubMedGoogle Scholar
- Lu J, Sundquist K, Baeckstrom D, Poulsom R, Hanby A, Meier-Ewert S, Jones T, Mitachell M, Pitha-Rowe P, Freemont P, Taylor-Papadimitriou J: A novel gene (PLU-1) containing highly conserved putative DNA/chromatin binding motifs is specifically up-regulated in breast cancer. J Biol Chem. 1999, 274: 15633-15645. 10.1074/jbc.274.22.15633View ArticlePubMedGoogle Scholar
- Dallas PB, Cheney IW, Liao D-W, Bowrin V, Byam W, Pacchione S, Kobayashi R, Yaciuk P, Moran E: P300/CREB binding protein – related protein p270 is a component of mammalian SWI/SNF complexes. Mol Cell Biol. 1998, 18: 3596-3603.PubMed CentralView ArticlePubMedGoogle Scholar
- Barton MC, Emerson BM: Regulated expression of the beta-globin gene locus in synthetic nuclei. Genes Dev. 1994, 8: 2453-2465.View ArticlePubMedGoogle Scholar
- Knapp M, Strober S, Liu C-P, Tucker PW, Blattner FR: Simultaneous Expression of Cμ and Cd Genes In a Cloned B Cell Line. Proc Natl Acad Sci USA. 1982, 79: 2996-3000. 10.1073/pnas.79.9.2996PubMed CentralView ArticlePubMedGoogle Scholar
- Landolfi NF, Capra JD, Tucker PW: Interaction of Cell-Type-Specific Nuclear Proteins with Immunoglobulin VH Promoter-Region Sequences. Nature. 1986, 323: 548-551. 10.1038/323548a0View ArticlePubMedGoogle Scholar
- Johnson DG, Carayannopoulos L, Capra JD, Hanke JH, Tucker PW: The ubiquitous octamer-binding protein(s) is sufficient for transcription of immunoglobulin genes. Mol Cell Biol. 1990, 10: 982-990.PubMed CentralView ArticlePubMedGoogle Scholar
- Buchanan KL, Hodgetts SI, Byrnes J, Webb CF: Differential transcription efficiency of two Ig VH promoters in vitro. J Immunol. 1995, 155: 4270-4277.PubMedGoogle Scholar
- Ito T, Tyler JK, Bulger M, Kobayashi R Kadonaga JT: ATP-facilitated chromain assembly with a nucleoplasmin-like protein from Drosophila melanogaster. J Biol Chem. 1996, 271: 2541-2548.Google Scholar
- Pazin MJ, Kadonaga JT: Chromatin: A Practical Approach. Edited by: Gould H. 1998, 173-194. Oxford: Oxford University Press,Google Scholar
- LeBowitz JH, Kobayashi L, Staudt L, Baltimore D, Sharp PA: Octamer binding proteins from B or Hela cells stimulate transcription of the immunoglobulin heavy-chain promoter in vitro. Genes Dev. 1988, 2: 1227-1237.View ArticlePubMedGoogle Scholar
- Takuhiro H, Wagner G: Using codon optimization, chaperone co-expression, and rational mutagenesis for production and NMR assignments of human eIF2a. J Mol NMR. 2004, 28: 357-367.View ArticleGoogle Scholar
- Sugai M, Gonda H, Nambu Y, Yoshifumi Y, Shimizu A: Accessibility control of recombination at the immunoglobulin locus. Cur Immunol Rev. 2005, 1: 69-79. 10.2174/1573395052952905.View ArticleGoogle Scholar
- Marecki S, McCarthy KM, Nikolajczyk BS: PU.1 as a chromatin accessibility factor for immunoglobulin genes. Mol Immunol. 2003, 40: 723-721. 10.1016/j.molimm.2003.08.007.View ArticleGoogle Scholar
- Scott M, Simon C, Anastasi J, Singh H: Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages. Science. 1994, 265: 1573-1577. 10.1126/science.8079170View ArticlePubMedGoogle Scholar
- Nelsen B, Tian G, Erman B, Gregoire J, Maki R, Graves B, Sen R: Regulation of lymphoid-specific immunoglobulin μ heavy chain gene enhancer by ETS-domain proteins. Science. 1993, 261: 82-86. 10.1126/science.8316859View ArticlePubMedGoogle Scholar
- Nikolajczyk BS, Cortes M, Feinman R, Sen R: Combinatorial determinants of tissue-specific transcription in B cells and macrophages. Mo Cell Biol. 1997, 17: 3527-3535.View ArticleGoogle Scholar
- Nikolajczyk BS, Sanchez JA, Sen R: ETS protein-dependent accessibility changes at the immunoglobulin mu heavy chain enhancer. Immunity. 1999, 11: 11-20. 10.1016/S1074-7613(00)80077-1View ArticlePubMedGoogle Scholar
- Choi JK, Shen CP, Radomska HS, Eckhardt LA, Kadesch T: E47 activates the Ig-heavy chain and TdT loci in non-B cells. EMBO J. 1996, 15: 5014-5021.PubMed CentralPubMedGoogle Scholar
- Greenbaum S, Zhuang Y: Identification of E2A target genes in B lymphocyte development by using a gene tagging-based chromatin immunoprecipitation system. Proc Natl Acad Sci USA. 2002, 99: 15030-15035. 10.1073/pnas.232299999PubMed CentralView ArticlePubMedGoogle Scholar
- Nikolajczyk WD, Sen R: Mechanisms of mu enhancer regulation in B lymphocytes. Cold Spring Harbor Symp Quant Biol. 1999, 64: 99-107. 10.1101/sqb.1999.64.99View ArticlePubMedGoogle Scholar
- Hecht A, Grunstein M: Mapping DNA interaction sites of chromosomal proteins using immunoprecipitation and polymerase chain reaction. Methods Enzymol. 1999, 304: 399-414.View ArticlePubMedGoogle Scholar
- Kadosh , Struhl K: Targeted recruitment of the Sin3-Rpd3 histone deacetylase complex generates a highly localized domain of repressed chromatin in vivo. Mol Cell Biol. 1998, 18: 5121-5127.PubMed CentralView ArticlePubMedGoogle Scholar
- Forrester WC, Fernandez LA, Grosschedl R: Nuclear matrix attachment regions antagonize methylation-dependent repression of long-range enhancer-promoter interactions. Genes Dev. 1999, 13: 3003-3014. 10.1101/gad.13.22.3003PubMed CentralView ArticlePubMedGoogle Scholar
- Oancea AE, Berru M, Shulman MJ: Expression of the (recombinant) endogenous immunoglobulin heavy-chain locus requires the intronic matrix attachment regions. Mol Cell Biol. 1997, 17: 2658-2668.PubMed CentralView ArticlePubMedGoogle Scholar
- Webb CF, Das C, Eaton S, Calame K, Tucker PW: Novel protein-DNA interactions associated with increased immunoglobulin transcription in response to antigen plus interleukin-5. Mol Cell Biol. 1991, 11: 5197-5205.PubMed CentralView ArticlePubMedGoogle Scholar
- Webb CF, Das C, Eneff KL, Tucker PW: Identification of a matrix-associated region 5' of an immunoglobulin heavy chain variable region gene. Mol Cell Biol. 1991, 11: 5206-5211.PubMed CentralView ArticlePubMedGoogle Scholar
- Gobel P, Montalbano A, Ayers N, Kompfner P, Dickinson L, Webb CF, Feeney AJ: High frequency of matrix attachment regions and cut-like protein x/CCAAT-displacement protein and B cell regulator of IgH transcription binding sites flanking Ig V region genes. J Immunol. 2002, 169: 2477-87.View ArticleGoogle Scholar
- Rajaiya J, Hatfield M, Nixon JC, Rawlings DJ, Webb CF: Bruton's tyrosine kinase regulates immunoglobulin promoter activation in association with the transcription factor Bright. Mol Cell Biol. 2005, 25: 2073-2084. 10.1128/MCB.25.6.2073-2084.2005PubMed CentralView ArticlePubMedGoogle Scholar
- Rajaiya J, Nixon JC, Ayers N, Desgranges ZP, Roy AL, Webb CF: Induction of immunoglobulin heavy chain transcription through the transcription factor Bright requires TFII-I. Mol Cell Biol. 2006, 26: 4758-4768. 10.1128/MCB.02009-05PubMed CentralView ArticlePubMedGoogle Scholar
- Webb CF, Smith EA, Medina KL, Buchanan KL, Smithson G, Dou S: Expression of Bright at two distinct stages of B lymphocyte development. J Immunol. 1998, 160: 4747-4754.PubMedGoogle Scholar
- Numata S, Claudio PP, Dean C, Giordano A, Croce CM: Bdp, a new member of a family of DNA-binding proteins, associates with the retinoblastoma gene product. Cancer Res. 1999, 59: 3741-3747.PubMedGoogle Scholar
- Zhang HS, Gavin M, Dahiya A, Postigo AA, Ma D, Luo RX, Harbour JW, Dean DC: Exit from G1 and S phase of the cell cycle is regulated by repressor complexes containing HDAC-Rb-hSWI/SNF and Rb-hSWI/SNF. Cell. 2000, 101: 79-89. 10.1016/S0092-8674(00)80625-XView ArticlePubMedGoogle Scholar
- Dignam JD, Lebovitz RM, Roeder RG: Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei. Nucleic Acids Res. 1983, 11: 1475-1489. 10.1093/nar/11.5.1475PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.