INTRODUCTION

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The immunoglobulin µ heavy-chain (IgH) gene enhancer (µ enhancer), located in the J_H-Cµ intron, is necessary for IgH gene expression in B lymphocytes (17, 23). The µ enhancer has also been shown to play a key role in the initiation of IgH gene rearrangements in the most immature B-cell precursors (2, 30, 32, 42). These observations indicate that detailed analysis of the µ enhancer will provide insights into the general problem of enhancer function as well as early regulatory events in B lymphopoiesis.

Studies using the murine µ enhancer have shown that the enhancer contains binding sites for several nuclear factors that mediate its transcription-activating function (6). µ enhancer binding proteins can be broadly classified into two groups: those whose expression is tissue restricted such as the µA, µB, and octamer motif binding proteins; and those whose expression is more ubiquitous, such as the basic helix-loop-helix (bHLH) family of transcription factors that bind the µE1 to µE5 motifs. How these two kinds of protein factors collaborate to produce a functional, cell-specific enhancer is unknown. Furthermore, mutation of individual motifs within the enhancer does not significantly affect enhancer activity, indicating a degree of functional redundancy among the various motifs that have been identified (16).

To simplify the analysis of this enhancer, we have previously described a minimal domain of the murine µ enhancer containing the µA, µB, and µE3 motifs that is active in B cells (24). Based on the observation that minimal enhancer activity depends on all three motifs, we proposed that this domain contains no redundant elements. The µA and µB elements bind the ETS domain proteins Ets-1 and PU.1, respectively, whereas the µE3 element binds several members of the bHLH-zip (leucine zipper-containing bHLH) family, such as TFE3 and USF. Thus, like the full µ enhancer, the minimal enhancer is composed of binding sites for tissue-restricted (PU.1) and ubiquitously expressed (TFE3 and USF) factors, suggesting that it is a good model in which to examine the mechanism of enhancer function. To strengthen the proposed importance of the minimal enhancer, in this study we examined the corresponding region of the intronic µ enhancer from the human IgH locus (11).

We found that the sequences of the µA and µB sites, as well as the spacing between them, were highly conserved between the two enhancers. Consistent with this observation, Ets-1 and PU.1 proteins bound to these sites. However, the intervening µE3 element was less well conserved between the two enhancers, and we detected no binding of either of two prototypic bHLH-zip proteins, TFE3 and USF, to the human enhancer. Because transcriptional activity of the minimal murine enhancer requires an intact µE3 site, we predicted that the lack of a µE3-like element in the human enhancer would render a corresponding minimal human enhancer fragment inactive in transfection assays. This was not the case. A µA/µB-containing region of the human enhancer was as active as the minimal murine enhancer in S194 plasma cells. Mutagenic analysis further showed that sequences between the µA and µB elements were necessary for enhancer activity, suggesting that the minimal human µ enhancer also required an element in addition to the ETS protein binding sites. We found that the intervening element bound the transcription factor CBF (core binding factor; also known as PEBP2 or AML1 [15, 39]), and binding was disrupted in all mutants that were inactive in transfection assays. These observations identify the first B-cell-specific target of CBF, a factor that has previously been implicated in the activation of several T and myeloid cell-specific promoters and enhancers (7, 12, 27, 35, 41, 44), and demonstrate that ETS-CBF is a common composite element in antigen receptor gene enhancers.

	MATERIALS AND METHODS

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Mammalian and bacterial expression plasmids. The PU.1 (pEVRF-PU.1), Ets-1 (pEVRF-Ets-1), and CBF2₄₅₁ [pcDNA/CBF2(451)] expression vectors have been previously described (5, 43). The bacterial expression plasmids His-PU.1 and His-ETS(Ets-1) are described in reference 25.

Construction of reporter plasmids. The µ70 dimer reporter was described previously (24). The murine and human µ51 wild-type (mWT and hWT) dimer reporters were constructed by ligating two tandem repeats of the annealed oligonucleotides 5' TCG ACC TGG CAG GAA GCA GGT CAT GTG GCA AGG CTA TTT GGG GAA GGG AAC 3' and 5' TCG AGT TCC CTT CCC CAA ATA GCC TTG CCA CAT GAC CTG CTT CCT GCC AGG 3' (mWT) and 5' TCG ACC TGG CAG GAA GCA GGT CAC CGC GAG AGT CTA TTT TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT AAA ATA GAC TCT CGC GGT GAC CTG CTT CCT GCC AGG 3' (hWT) into the 56CAT enhancerless reporter plasmid digested with SalI. The human µ51 mutant (hM1 to hM6) and murine µC (mµC) reporters were constructed similarly with the following annealed oligonucleotides: hM1, 5' TCG ACC TGG CAG GAA GCA ttg CAC CGC GAG AGT CTA TTT TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT AAA ATA GAC TCT CGC GGT Gca aTG CTT CCT GCC AGG 3'; hM2, 5' TCG ACC TGG CAG GAA GCA GGT ata CGC GAG AGT CTA TTT TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT AAA ATA GAC TCT CGC Gta tAC CTG CTT CCT GCC AGG 3'; hM3, 5' TCG ACC TGG CAG GAA GCA GGT CAt atg GAG AGT CTA TTT TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT AAA ATA GAC TCT Cca taT GAC CTG CTT CCT GCC AGG 3'; hM4, 5' TCG ACC TGG CAG GAA GCA GGT CAC Ctc tAG AGT CTA TTT TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT AAA ATA GAC TCT aga GGT GAC CTG CTT CCT GCC AGG 3'; hM5, 5' TCG AGT TGG CAG GAA GCA GGT CAC CGC GAG gta CTA TTT TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT AAA ATA Gta cCT CGC GGT GAC CTG CTT CCT GCC AGG 3'; hM6, 5' TCG ACC TGG CAG GAA GCA GGT CAC CGC GAG AGT CTA ccc TAG GAA GCA AAC 3' and 5' TCG AGT TTG CTT CCT Agg gTA GAC TCT CGC GGT GAC CTG CTT CCT GCC AGG 3'; and mµC, 5' TCG ACC TGG CAG GAA GCA GGT CAT GTG GaA AGG CTA TTT GGG GAA GGG AAC 3' and 5' TCG AGT TCC CTT CCC CAA ATA GCC TTt CCA CAT GAC CTG CTT CCT GCC AGG 3'. The mutated nucleotides are in lowercase and underlined. All reporter plasmids were sequenced to ensure that the appropriate mutations were introduced.

Cell culture, transfections, and CAT assays. S194 cells were grown in RPMI medium supplemented with 5% newborn serum, 5% inactivated fetal calf serum, and 50 µg each of penicillin and streptomycin per ml. M12 cells were grown in RPMI medium supplemented with 10% inactivated fetal calf serum and 50 µg each of penicillin and streptomycin per ml. Murine and human dimeric enhancer-containing chloramphenicol acetyltransferase (CAT) reporter plasmids (5 µg) were transfected into S194 and M12 cells by the DEAE-dextran method as previously described (24); 40 to 48 h after transfection, whole-cell extracts were prepared by three rounds of freeze-thawing, and the levels of CAT protein in the extracts were determined by CAT enzyme-linked immunosorbent assay (ELISA) (Boehringer Mannheim Corp.) according to the manufacturer's instructions.

In vitro protein expression, EMSAs, and supershifts. Full-length PU.1 and the ETS domain of Ets-1 [Ets-1(ETS)] proteins were expressed as hexahistidine-tagged proteins (25). Full-length TFE3 and USF proteins were expressed as GST fusion proteins and were purified as described by the manufacturer (Pharmacia Biotech, Inc.) The CBF2_41-190 and CBF2_41-214 proteins containing the DNA binding Runt domain of CBF2 were prepared as previously described (3). For electrophoretic mobility shift assays (EMSAs), either bacterially expressed and purified proteins or 4, 8, and 16 µg of S194 nuclear extracts were incubated with ³²P-labeled oligonucleotide DNA probes (20,000 cpm) in the presence of 25 ng of poly(dI-dC) · (dI-dC) (1 µg for extracts), 70 mM NaCl, and 10% glycerol for 10 min at room temperature, and reactions were resolved on a 4% polyacrylamide gel. Wild-type and mutant probes in each experiment were of comparable specific activity. EMSAs in Fig. 5, 6, 8, and 9 were performed with annealed double-stranded oligonucleotides, whereas those in Fig. 7 were performed with PstI-BamHI fragments from the murine enhancer (bp 380 to 433) as described elsewhere (24). The CBF high-affinity consensus probe used for Fig. 8 was obtained by annealing two oligonucleotides, 5'-AAT TCG AGT ATT GTG GTT AAT ACG-3' and 5'-AAT TCG TAT TAA CCA CAA TAC TGG-3'. Supershifts were performed by incubating 20 µg of S194 or 27 µg of 70Z extracts with ³²P-labeled oligonucleotide DNA probes (50,000 cpm) for 20 min at room temperature, followed by incubation with the specified antibodies for an additional 30 min on ice (21, 22).

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

The human µ enhancer does not contain a µE3 element. To extend our ongoing characterization of the murine IgH µ enhancer, we examined the organization of the human µ enhancer. Of the several bHLH protein binding sites known in the murine enhancer, µE1, µE2, and µE4 were easily recognizable in the human enhancer (Fig. 1). Although the µE5 and µE3 sites showed regions of similarity, they were significantly less conserved (Fig. 1). Specifically, the regions corresponding to both the µE3 and µE5 sites lacked one half of the minidyad that is characteristic of the µE elements. In contrast, the lymphoid cell-restricted elements µA, µB, and octamer were highly conserved between the two enhancers, as was the spacing between the µA and µB elements (Fig. 1). Thus, two of the three elements present in the minimal murine enhancer (consisting of µA, µB, and µE3 elements) were conserved in the human sequence.

View larger version (38K): [in this window] [in a new window]   FIG. 1.   Alignment of IgH µ enhancer sequences. Sequences of IgH µ enhancer from four different species (GenBank accession no. V01523 for mouse, M13799 for rat, K01901 for human, and X13700 for rabbit) were aligned by using the Pileup program in the Wisconsin package version 8.1 (Genetics Computer Group, Madison, Wis.). Elements containing previously identified recognition motifs are overlined, and positions where the nucleotides from all species are identical are indicated by asterisks.

View larger version (67K): [in this window] [in a new window]   FIG. 2.   DNA binding analysis of PU.1, Ets-1, TFE3, and USF1 to the murine and human enhancers. The human (H) and murine (M) µ enhancer probes were used in binding assays with the following: lanes 1 and 2, His-PU.1 (80 ng); lanes 3 and 4, His-PU.1 (160 ng); lanes 5 and 6, Ets-1(ETS) (100 ng); lanes 7 and 8, Ets-1(ETS) (200 ng); lanes 9 and 10, GST-TFE3 (50 ng); and lanes 11 and 12, GST-USF1 (40 ng). Arrows: 1 and 2, USF and TFE3 binding to the murine probe only; 3, PU.1-DNA complex; 4, Ets-1(ETS)-DNA complex. EMSAs were performed as described previously (5).

Functional analysis of the minimal human µ enhancer. Our earlier analysis of the minimal murine µ enhancer showed that mutation of the µE3 site significantly decreased enhancer activity in B cells. Absence of a µE3-like element in the human µ enhancer suggested that a corresponding fragment of this enhancer would have very low enhancer activity, similar to that of the µE3 mutated murine enhancer. To check if this was so, we tested the transcription activation properties of a µA/µB-containing fragment of the human enhancer. Synthetic oligonucleotides encompassing the µA/µB elements from the human enhancer were cloned as dimers 5' of a CAT reporter gene transcribed from a c-fos gene promoter and assayed by transient transfection in S194 plasma cells. Surprisingly, this human µ enhancer fragment was as active as the minimal murine µ70 enhancer in S194 plasma cells (Fig. 3) but not in nonlymphoid cells (data not shown). As expected, high-level activity of the murine enhancer was dependent on the µE3 site because a µE3 mutation significantly decreased activity. We conclude that despite the absence of a recognizable µE3-like element that can bind bHLH-zip proteins such as TFE3 and USF, a fragment of the human enhancer spanning the µA and µB sites is a functional B-cell-specific enhancer, which we shall refer to as the minimal human enhancer.

View larger version (11K): [in this window] [in a new window]   FIG. 3.   The minimal murine and human IgH µ enhancers activate transcription comparably. Reporter plasmids (5 µg) containing dimeric murine µ70 [(µ70)2], murine µE3 mutant (µE3), and human [h(µ51)2] enhancers were transfected into S194 plasma cell lines, and CAT assays were performed by ELISA as described in Materials and Methods. CAT enzyme activity is shown on the y axis as the percentage of the amount of CAT enzyme obtained with the dimeric murine µ70 reporter. Results show the averages of at least two transfections carried out in duplicate. 56 refers to an enhancerless reporter. Error bars indicate the average deviations of the data.

View larger version (27K): [in this window] [in a new window]   FIG. 4.   Identification of an element in the human IgH enhancer in the region corresponding to the murine µE3 motif. (A) Comparison of the murine and human enhancers indicating the absence of a µE3 motif in the human enhancer. The µA, µE3, and µB motifs are indicated in boldface, and the nucleotide numbers of the murine and human enhancers are from references 8 and 11, respectively. (B) Sequences of a panel of mutants in the human enhancer (hM1 to hM6) corresponding to the region spanning the murine µE3 motif. The altered sequence in each mutant is indicated in lowercase and underlined. (C) Transcriptional activities of the minimal human mutant enhancers. Reporter plasmids (5 µg) containing dimeric wild-type hWT and mutant (hM1 to hM6) enhancers were transfected into S194 plasma cell lines, and CAT assays were performed by ELISA as described in Materials and Methods. CAT enzyme activity is shown on the y axis as the percentage of the activity of the reporter plasmid containing the hWT enhancer. Results shown are the averages of at least two transfections carried out in duplicate. Error bars indicate the average deviations of the data.

View larger version (48K): [in this window] [in a new window]   FIG. 5.   DNA binding of PU.1 and Ets-1 to the human enhancer mutants. EMSAs were carried out with bacterially expressed and purified His-Ets-1(ETS) (lanes 1 to 6) and His-PU.1 (lanes 7 to 12) proteins and hWT and mutant enhancer probes as indicated above the lanes. The mutant probes are numbered as in Fig. 4B. Specific nucleoprotein complexes are indicated by arrows 1 [His-Ets-1(ETS)-DNA] and 2 (His-PU.1-DNA). A lower-mobility complex in the lanes with the PU.1 protein is due to the double occupancy of the µB and µA sites.

Analysis of proteins binding to the human µ enhancer. Close examination of the human sequence revealed a similarity to the recognition site of CBF, the consensus binding site for which is PyGPyGGT (15, 19, 37). On the noncoding strand of the human enhancer, the nucleotides corresponding to the murine µE3 motif are 5'-CGCGGT-3' (Fig. 1). We therefore tested whether CBF2 (the DNA binding subunit of CBF) bound to the human enhancer fragment.

View larger version (23K): [in this window] [in a new window]   FIG. 6.   CBF2 binds the human IgH µ enhancer in vitro. (A) EMSAs were carried out with bacterially expressed and purified CBF241-190, which contains the DNA binding Runt domain of CBF2, and hWT and mutant enhancer probes as indicated. Specific nucleoprotein complexes in lanes 1, 2, 5, and 6 are indicated by an arrow. (B) In vitro competition assays with CBF241-190 bound to the human WT probe. EMSAs were carried out as described in the text, with 25-, 125-, and 250-fold molar excesses of competitor DNA fragments indicated by triangles. Competitor DNA was excised as dimeric fragments from reporter plasmids used for transfections in Fig. 4C and contain wild-type or mutated human enhancer sequences as indicated.

The murine enhancer also binds CBF. The results presented above were consistent with the idea that the minimal domain of the human enhancer examined here is activated by ETS domain proteins binding to µA and µB sites and a CBF family member binding to the intervening sequence. The human enhancer has two features that are similar to the murine enhancer: it requires µA and µB binding proteins, and three protein binding sites are required for transcriptional activity. The major difference between the two is that the murine enhancer is believed to be activated by bHLH-zip proteins such as TFE3, whereas the human enhancer does not bind TFE3 and may be activated by CBF. Although it was possible that ETS domain proteins combined with different factors to activate the two enhancers, we tested whether CBF binding was a common feature of both enhancers. Fragments of the wild-type murine enhancer and mutations thereof were assayed for CBF binding by EMSA. The wild-type sequence as well as mutants µA and µB bound CBF2 in vitro (Fig. 7, lanes 1, 2, and 4); however, mutant µE3 did not (Fig. 7, lane 3). We conclude that the murine enhancer contains a CBF binding site between the µA and µB elements, which is lost in mutant µE3. Thus, CBF binding is a common feature of both enhancers.

View larger version (51K): [in this window] [in a new window]   FIG. 7.   CBF2 binds the murine IgH µ enhancer in vitro. EMSAs were carried out with bacterially expressed and purified CBF241-190, which contains the DNA binding Runt domain of CBF2, and the mWT µ enhancer and µA, µE3, and µB mutant enhancer probes as indicated.

The µ enhancers bind CBF present in B-cell nuclear extracts. To detect CBF DNA binding activity in B-cell extracts, we used a high-affinity CBF binding site in EMSA. In S194 plasma cell extracts, a discrete nucleoprotein complex was detected with this probe (Fig. 8A, lane 1). This complex was specific, because it could be competed with the self oligonucleotide (Fig. 8A, lanes 8 and 9) but not with a high-affinity Ets-1 binding site (Fig. 8A, lanes 10 to 12). The murine and human enhancer sequences also competed this complex (Fig. 8A, lanes 2 to 4 and 5 to 7, respectively), although approximately fourfold-higher levels were required compared to the self competitor. Furthermore, a murine enhancer fragment containing a mutated µE3 element did not compete for CBF binding in S194 extracts (data not shown). We conclude that the murine and human Ig enhancer sequences bind endogenous B cell CBF with comparable affinities.

View larger version (58K): [in this window] [in a new window]   FIG. 8.   The murine and human µ enhancers bind CBF in B-cell nuclear extracts. (A) In vitro competition assays with CBF bound to a high-affinity consensus binding probe. EMSAs were carried out with 20 µg of S194 nuclear extracts with 32P-labeled CBF oligonucleotide DNA probes (50,000 cpm), in the presence of no competitor DNA (lane 1), 5-, 25-, and 133-fold molar excesses of murine µ enhancer DNA (lanes 2 to 4) and human µ enhancer DNA (lanes 5 to 7), and 8- and 33-fold molar excesses of self (lanes 8 and 9) and 16-, 32-, and 66-fold molar excesses of nonspecific (lanes 10 to 12) competitor oligonucleotides, indicated by triangles. Specific nucleoprotein complexes are indicated by an arrow. The nonspecific competitor is a high-affinity binding site for Ets-1 (28). (B) Supershift EMSAs were carried out with 20 µg of S194 plasma cell and 27 µg of 70Z pre-B-cell extracts and a CBF high-affinity consensus binding site probe. Lanes 1 to 5 show complexes formed by the incubation of S194 extracts with CBF probes followed by no antiserum (lane 1), antiserum specific for AML-1, -2, and -3 (lanes 2, 3, and 4, respectively), and normal rabbit serum (NRS) (lane 5). Lanes 6 to 10 show complexes formed by the incubation of 70Z extracts with CBF probes followed by no antiserum (lane 6), antiserum specific for AML-1, -2, and -3 (lanes 7, 8, and 9, respectively), and normal rabbit serum (lane 10). Specific complexes are indicated by an arrow on the left.

CBF binding correlates with both murine and human enhancer activities. Analysis of the human enhancer suggested that ETS domain proteins plus CBF are sufficient to generate transcriptional activity in B cells. Furthermore, the murine enhancer was found to contain a CBF binding site that overlapped the µE3 site. It is likely that CBF binds to the TGTGG motif of the murine enhancer, which is also a part of the CATGTGG recognition site of bHLH-zip proteins. Because the µE3 mutation also eliminated CBF binding, we could not ascertain whether CBF and bHLH-zip proteins (such as TFE3) could both provide the third essential component to the tripartite enhancer. Ideally we wanted to analyze an enhancer that bound TFE3, but not CBF, to determine whether bHLH-zip proteins could confer the observed properties of this enhancer. In an attempt to distinguish between CBF and TFE3 binding to the murine enhancer, we mutated the C residue 3' of the CBF core recognition site to an A (Fig. 9A), because previous studies showed that TGTGGA was recognized poorly by CBF2 (37). This mutation, we anticipated, would substantially reduce affinity for CBF binding while retaining TFE3 binding. Fortuitously, an analogous situation was created in the hM3 human enhancer mutation, where the sequence CATATGG is similar to the murine µE3 site and may therefore bind TFE3 (Fig. 9A).

View larger version (31K): [in this window] [in a new window]   FIG. 9.   CBF2 binding correlates with minimal µ enhancer activity in B-cell lines. (A) Sequences of murine and human wild-type enhancers compared to sequences of two mutants in the murine (mµC) and human (hM3) enhancers. The overlapping µE3 (bHLH-zip protein binding) and µC (CBF binding) sites in the murine enhancer are overlined and underlined, respectively. The murine µC mutation alters the single nonoverlapping base between the two motifs. This position in the CBF2 consensus binding site has been shown to be important for binding (19). The µC motif in the human motif is also underlined and is shown to be mutated in the hM3 mutation, which introduces an E-box motif into the human enhancer sequence that is absent in the wild-type sequence. (B) EMSAs were carried out with bacterially expressed and purified GST-TFE3, CBF241-214, and S194 plasma cell extracts and the indicated murine and human probes. Lanes 1 to 4 show complexes formed by the incubation of approximately 50 ng of GST-TFE3 with the indicated probes. Specific complexes in lanes 1, 2, and 4 are indicated by the top arrow on the left, and a nonspecific complex is indicated by an asterisk. Lanes 5 to 8 show complexes formed by the incubation of 100 ng of CBF241-214 and the indicated probes. Specific nucleoprotein complexes in lanes 5 and 7 are indicated by the bottom arrow on the left. Lanes 9 to 11 and 12 to 14 show complexes formed by the incubation of 4, 8, and 16 µg of S194 extracts, respectively, with the mWT and mµC probes. The µE3 binding complex is indicated by the arrow on the right. (C) Transcriptional activity of the murine enhancer. Reporter plasmids (5 µg) containing dimeric murine wild-type [WT or (µ70)2] and mutant (µC) enhancers or no enhancer (56) were transfected into the M12 B-cell line, and CAT assays were performed by ELISA as described in the Materials and Methods. CAT enzyme activity is shown on the y axis as the percentage of the activity of the reporter plasmid containing the wild-type murine (µ70)2 enhancer. Results shown are the averages of at least two transfections carried out in duplicate. Error bars indicate the average deviations of the data.

CBF2 plus Ets-1 activate the µ enhancer in nonlymphoid cells. The preceding analysis suggested that CBF may work together with ETS proteins to activate the minimal µ enhancer. To obtain further supporting evidence, we assayed the ability of CBF2 to transactivate the µ enhancer fragment in nonlymphoid cells. In HeLa cells, the µ70 enhancer was activated about 10-fold by coexpression of PU.1 and Ets-1 (Fig. 10, compare first and last bars). In the presence of PU.1, Ets-1, and CBF2, significantly higher transcriptional activity was observed (Fig. 10, bar 2) which required all three elements in the enhancer to be intact (Fig. 10, bars 3 to 5). Of the three mutations, the µB mutation had the weakest effect, presumably because exogenously expressed Ets-1 and CBF2 (µA and µE3 binding proteins, respectively) partially reduced the requirement for the µB site in the cotransfection assay. Similar effects were observed when only Ets-1 and TFE3 were coexpressed, resulting in µB-independent activation of µ70 (unpublished observations). Consistent with the mutational analysis, Ets-1 plus CBF2 transactivated the µ70 enhancer, whereas PU.1 and CBF2 did not (data not shown). These results indicate that CBF2 may be a functional µ enhancer binding protein.

View larger version (12K): [in this window] [in a new window]   FIG. 10.   CBF2 activates the IgH µ enhancer in nonlymphoid cells in cooperation with Ets-1. HeLa cells were transfected with reporter plasmids containing the (µ70)2 enhancer along with expression plasmids for PU.1 (2 µg) and Ets-1 (2 µg) (bar 1) and for PU.1 (1 µg), Ets-1 (1 µg), and CBF2 (2 µg) (bar 2) or with an empty pEVRF2 expression plasmid as carrier DNA (bar 6). The transcription activation abilities of PU.1 (1 µg), Ets-1 (1 µg), and CBF2 (2 µg) were also tested by cotransfecting these reporter plasmids with binding site mutant versions of the (µ70)2 enhancer, µA (bar 3), µE3 (bar 4), and µB (bar 5). Cells were harvested 2 days after being transfected, and CAT analysis was performed by ELISA. Results shown are the averages of at least two transfections carried out in duplicate. Error bars indicate the average deviations of the data.

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

We have previously defined a functional domain of the murine IgH gene enhancer that contains the µA and µB motifs that bind ETS domain proteins and the µE3 element that binds several ubiquitously expressed bHLH-zip proteins. All three elements are required for activity of this domain in transient transfection assays. Here we describe the analysis of the corresponding region of the human IgH enhancer. Both µA and µB sites were highly conserved between the two enhancers; however, the intervening µE3 element was not. Lack of sequence similarly in this region was reflected in the inability of prototypic bHLH-zip proteins TFE3 and USF to bind to the human enhancer. However, in striking contrast to the µE3 mutated murine enhancer that is inactive in transfection assays, the human enhancer domain was an active transcriptional enhancer in B cells. Nucleotides between the µA and µB motifs were necessary for enhancer activity and were found to bind the transcription factor CBF. Furthermore, we also found that the µE3 element of the murine enhancer was a CBF binding site. These observations highlight the similarity in organization of the murine and human enhancers, particularly with respect to the core enhancer domain. The CBF binding site in the Ig µ enhancers will be referred to as the µC element.

Although it has been assumed that the murine µE3 sequence works by binding bHLH-zip proteins, our observation that this element is also a CBF binding site raised the question of whether TFE3-like proteins or CBF family members were the functional µE3 binding proteins. Based on the analysis of the murine and human enhancers and several mutants thereof and transactivation studies, we propose that CBF2 is likely to be the common, functional protein required to generate transcriptional activity in B cells. Is TFE3 binding to the murine sequence, then, a complete coincidence, or do these proteins also activate the enhancer under some circumstances? Reexamination of the early in vivo footprint experiments of Ephrussi et al. (4) provides some interesting ideas. They observed protections over the bHLH protein binding sites of the murine µ enhancer, including the µE3 motif, in plasmacytoma cells, which represent the terminal stage of B-cell differentiation. Indeed, the residues that scored in the assay are reminiscent of TFE3-µE3 interactions and unlike the expected pattern for CBF2. Specifically, only two of three guanosines on the coding strand were protected by dimethyl sulfate in vivo and by TFE3 proteins in vitro, whereas methylation interference assays with CBF2 would be expected to identify all three guanosines. Furthermore, no protections were seen over the µA and µB elements in the in vivo footprinting studies, even though these sites are crucial for enhancer activity in transfection experiments. The recent analysis of TFE3-deficient mice in which serum Ig levels are reduced indicates a defect in terminal B-cell differentiation (20). One possibility is that activation of the enhancer requires ETS and CBF proteins at earlier stages of B-cell differentiation, and in later stages of differentiation such as plasma cells, enhancer activity is maintained by bHLH proteins such as TFE3. Our observation that TFE3 and Ets-1 can interact directly as well as transactivate the µ enhancer is consistent with the possibility that bHLH-zip proteins also play a role in µ enhancer regulation (unpublished data).

CBF has been previously implicated in the regulation of T and myeloid cell-specific genes (1, 27, 36, 44). Since its identification as the protein that confers T-cell tropism to transformation by Moloney murine leukemia virus (34), CBF binding sites have been found in the enhancers of all the T-cell receptor (TCR) genes (7, 10, 12, 14, 41). Interestingly, CBF binding sites in both TCR and - enhancers are close to sites that bind ETS proteins. T-cell-specific activity of the TCR enhancer depends on an ATF/CREB site, a LEF binding site, and a composite ETS-CBF element (7). It is likely that T-cell specificity is largely determined by the LEF site which also binds TCF-1, a T-cell-restricted factor (38, 40). In the TCR enhancer, two ETS-CBF elements have been identified, and our recent experiments suggest that both elements plus an additional element between them are necessary for enhancer activity in T-cell lines (1a). The elements that confer T-cell specificity to the TCR enhancer are not known. Our identification of an ETS-CBF composite motif in the Ig µ enhancer suggests that this is a common element that regulates both B- and T-cell antigen receptor genes. An interesting possibility is that the ETS-CBF motif is a hematopoietic cell-specific element whose activity is further modulated in a lineage (or developmental stage)-specific manner by other factors.

Two differences may be noted in the organization of ETS-CBF motifs in the TCR enhancers compared to the IgH µ enhancer. First, the ETS and CBF binding sites in both TCR and - enhancers are close together, whereas the µA and µC motifs of the µ enhancer are well separated. For example, the ETS-CBF motif in the E4 element of the TCR enhancer has the sequence GGATGTGG, and the µA/µC sequence is shown in Fig. 1. Second, both TCR enhancers contain a second CBF site very close to the ETS-CBF element (this results in an ETS/CBF/CBF element in the TCR enhancers), whereas the µ enhancer contains a second ETS site (µB), making it an ETS-CBF/ETS-dependent regulatory sequence. It is likely that the second ETS site in the µ enhancer confers cell specificity by binding the B-cell- and macrophage-specific transcription factor PU.1. We have recently shown that the µA/µE3/µB enhancer activates transcription in B cells as well as macrophage cell lines (26) but not in T cells (unpublished observations), strengthening the idea that the µB site may specify transcriptional activation within hematopoietic cell types.

One of the genes encoding DNA binding  subunits of CBF (also known as PEBPA2B or AML1) is targeted in the most prevalent form of chromosomal translocation, t(12;21), identified in childhood acute lymphoblastic leukemias (9, 31, 33). The resulting TEL-AML1 fusion protein contains an N-terminal region derived from the ETS domain gene, TEL, which is fused to AML1 coding sequences that include the DNA binding Runt homology domain. Thus, the oncoprotein retains the ability to bind to CBF binding sites, and it is hypothesized that dysregulation of CBF-dependent gene regulation is a major factor in the development of disease (13). Because the leukemia induced by the t(12;21) translocation is one of immature B cells (9, 31, 33), CBF is likely to be important in early B-cell gene expression. Furthermore, in mice carrying a targeted disruption of the Cbfa2 (murine AML1) gene, both B- and T-cell development is blocked, reemphasizing the importance of this factor in lymphopoiesis (29) (unpublished observations). However, no CBF-regulated B-cell genes had been previously identified. Our studies are the first to identify a B-cell-specific enhancer that may be a target of CBF and highlight the combinatorial mechanisms by which ETS-CBF composite elements may be used to regulate B- and T-cell-specific gene expression.