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   <subfield code="a">Swapped green algal promoters: aphVIII -based gene constructs with Chlamydomonas flanking sequences work as dominant selectable markers in Volvox and vice versa</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[A. Hallmann, S. Wodniok]</subfield>
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   <subfield code="a">Production of transgenic organisms is a well-established, versatile course of action in molecular biology. Genetic engineering often requires heterologous, dominant antibiotic resistance genes that have been used as selectable markers in many species. However, as heterologous 5′ and 3′ flanking sequences often result in very low expression rates, endogenous flanking sequences, especially promoters, are mostly required and are easily obtained in model organisms, but it is much more complicated and time-consuming to get appropriate sequences from less common organisms. In this paper, we show that aminoglycoside 3′-phosphotransferase gene (aphVIII) based constructs with 3′ and 5′ untranslated flanking sequences (including promoters) from the multicellular green alga Volvox work in the unicellular green alga Chlamydomonas and flanking sequences from Chlamydomonas work in Volvox, at least if a low expression rate is compensated by an enforced high gene dosage. This strategy might be useful for all investigators that intend to transform species in which genomic sequences are not available, but sequences from related organisms exist.</subfield>
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   <subfield code="a">Springer-Verlag, 2006</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Green algae</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Volvocales</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Recombinant DNA technology</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Transgenic expression</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Genetic transformation</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Paromomycin resistance</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">aphVIII : Aminoglycoside 3′-phosphotran sferase (VIII) gene</subfield>
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   <subfield code="a">hsp70A : Heat shock protein 70A ge ne</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">rbcS2 : Ribulose-1,5-bisphosphat-carboxylase small subunit gene 2 from Chlamydomonas reinhardtii</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">rbcS3 : Ribulose-1,5-bisphosphat-carboxylase small subunit gene 3 from Volvox carteri</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">UTR : Untranslated region</subfield>
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   <subfield code="a">Hallmann</subfield>
   <subfield code="D">A.</subfield>
   <subfield code="u">Department of Cellular and Developmental Biology of Plants, University of Bielefeld, Universitätsstr 25, 33615, Bielefeld, Germany</subfield>
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   <subfield code="u">Department of Cellular and Developmental Biology of Plants, University of Bielefeld, Universitätsstr 25, 33615, Bielefeld, Germany</subfield>
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   <subfield code="t">Plant Cell Reports</subfield>
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   <subfield code="g">25/6(2006-06-01), 582-591</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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