Abstract

Expression of the chicken globin genes is regulated in part by competition between the betaA-globin and epsilon-globin promoters for the enhancer found between the genes. To understand the determinants of the enhancer-promoter interaction in stage-specific regulation, the functional elements of the embryonic chicken epsilon-globin promoter were characterized. In vitro assays demonstrated that: (a) the TATA motif at -30 bound GATA-1, (b) Sp1 bound to an element centered at -54, and (c) both Sp1 and another factor, designated CACCC (which appears related to erythroid Krüppel-like factor, EKLF) bound in the -120 to -128 region. The functions of these motifs were tested using transient expression in embryonic erythroid cells. In the absence of the enhancer, promoter point mutants showed that the TATA, Sp1, and CCAAT motifs (but not the CACCC motif) contributed to promoter activity. In contrast, in the presence of the enhancer, all four motifs (including the CACCC motif) contributed to transcription. Developmental regulation of the enhancer activity was observed, with enhancement decreasing sharply from 185-fold at 4 days (cells expressing epsilon-globin) to 16-fold at 10 days (when epsilon-globin is no longer expressed). Taken together, the data suggest that multiple transcription factors contribute to promoter-enhancer interaction and the developmental regulation of epsilon-globin expression, with EKLF-like factors having an especially important role. Regulation of stage specificity occurs at the level of enhancer/epsilon-promoter interaction, even in the absence of competition, and is not simply a property of the enhancer or promoter in isolation.

Highlights

  • Interaction between the individual globin genes and distant regulatory elements is important for this process

  • The locus control region (LCR) is needed for developmental regulation of the individual globin genes, whose promoters are thought to compete for interaction with the LCR (8 –11)

  • Mutation of the TATA element (G 3 T at Ϫ33, oligonucleotide Am33) destroyed the GATA motif and prevented formation of the GATA-11⁄7DNA complex (Fig. 4, lanes 7–10). These results indicate that the cGATA-1 protein binds to the GATA/TATA motif of the ⑀ promoter

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Summary

THE JOURNAL OF BIOLOGICAL CHEMISTRY

Vol 271, No 41, Issue of October 11, pp. 25459 –25467, 1996 Printed in U.S.A. Identification of Functional Elements of the Chicken ⑀-Globin Promoter Involved in Stage-specific Interaction with the ␤/⑀ Enhancer*. To understand the determinants of the enhancer-promoter interaction in stage-specific regulation, the functional elements of the embryonic chicken ⑀-globin promoter were characterized. In vitro assays demonstrated that: (a) the TATA motif at ؊30 bound GATA-1, (b) Sp1 bound to an element centered at ؊54, and (c) both Sp1 and another factor, designated CACCC (which appears related to erythroid Kruppel-like factor, EKLF) bound in the ؊120 to ؊128 region The functions of these motifs were tested using transient expression in embryonic erythroid cells. Unlike the human cluster, a strong enhancer (the ␤/⑀ enhancer), with LCR-like properties, is located inside the cluster, between the ␤A- and ⑀-globin genes (18 –20) Both the upstream sites and the ␤/⑀ enhancer contribute to the expression of all the genes in the cluster [21]. To understand more about stage-specific regulation, we have undertaken a detailed characterization of the ⑀-globin promoter and its interaction with the ␤/⑀ enhancer at different developmental stages

EXPERIMENTAL PROCEDURES
RESULTS
DISCUSSION

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