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    <title>Wall, L.</title>
    <link>http://repub.eur.nl/res/aut/4611/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Two tissue-specific factors bind the erythroid promoter of the human porphobilinogen deaminase gene. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2434/</link>
      <pubDate>1989-01-01T00:00:00Z</pubDate>
      <description>We have studied the erythroid-specific promoter of the human gene coding for Porphobilinogen Deaminase (PBGD) by DNaseI footprinting, gel retardation and methylation interference assays. We show that this promoter, which is inducible during MEL cell differentiation, contains three binding sites for the erythroid-specific factor NF-E1 and one site for a second erythroid-specific factor, which we name NF-E2. NF-E1 is a factor that also binds the promoter and the enhancer (present in the 3' flanking region) of the human beta-globin gene. NF-E2 has not yet been described and although it binds to a sequence containing the Ap1 consensus, it appears to be different from Ap1.</description>
    </item> <item>
      <title>The human β-globin gene 3' enhancer contains multiple binding sites for an erythroid specific protein. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2431/</link>
      <pubDate>1988-01-01T00:00:00Z</pubDate>
      <description>We have shown that the minimal enhancer fragment present in the 3'-flanking region of the human beta-globin gene contains four regions that bind nuclear proteins in vitro. By using gel mobility shift and DNase I footprinting assays, we were able to show that each of these regions binds an erythroid-cell-specific nuclear factor which we name NF-E1. This factor is present in erythroid cells at different developmental stages of globin gene expression. The recognition sequence of this protein (A/C Py T/A ATC A/T Py) is also present in the intragenic enhancer and the promoter of the beta-globin gene as well as in the promoter of other erythroid-cell specific genes. In addition to NF-E1, each of the four binding regions interacts with at least one other protein factor.</description>
    </item> <item>
      <title>The human β-globin gene promoter; nuclear protein factors and erythroid specific induction of transcription. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2432/</link>
      <pubDate>1988-01-01T00:00:00Z</pubDate>
      <description>We have shown that the promoter of the human beta-globin gene contains three regions in addition to the known CAC, CAAT and TATA box regions that are important for the induction of transcription in erythroid cells. By using DNaseI footprinting and gel mobility shift assays we were able to show that two of these regions bind the erythroid specific nuclear factor NF-E1 (and ubiquitous factors). The third region binds a ubiquitous CAAT-box factor (CP1). Deletion experiments suggest that only the combination of NF-E1 and CP1 binding sites, but not each of the sites alone, are capable of mediating the induction of transcription of a minimal (CAC, CAAT, TATA box) beta-globin promoter in mouse erythroleukaemia (MEL) cells.</description>
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