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Hallmann, A. ; Sumper, Manfred

Reporter genes and highly regulated promoters as tools for transformation experiments in Volvox carteri

Hallmann, A. und Sumper, Manfred (1994) Reporter genes and highly regulated promoters as tools for transformation experiments in Volvox carteri. Proc. Nati. Acad. Sci. USA (PNAS) 91 (24), S. 11562-11566.

Veröffentlichungsdatum dieses Volltextes: 09 Dez 2010 09:44
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.18678


Zusammenfassung

The multicellular alga Volvox is an attractive model for the study of developmental processes. With the recent report of successful transformation, regulated promoters as well as reporter genes working in this organism are now required. The Volvox genes encoding arylsulfatase and the extracellular glycoprotein ISG are strictly regulated. The former is transcribed only under conditions of sulfur ...

The multicellular alga Volvox is an attractive model for the study of developmental processes. With the recent report of successful transformation, regulated promoters as well as reporter genes working in this organism are now required. The Volvox genes encoding arylsulfatase and the extracellular glycoprotein ISG are strictly regulated. The former is transcribed only under conditions of sulfur starvation, whereas the latter operates under extreme developmental control--i.e., it is transcribed for only a few minutes in Volvox embryos at the stage of embryonic inversion. The gene encoding the sexual pheromone of Volvox carteri was placed under the control of the arylsulfatase promoter. In response to sulfur deprivation, V. carteri transformed by this construct synthesized and secreted biologically active pheromone. In addition, the gene encoding Volvox arylsulfatase was placed under the control of the ISG promoter. Transformed algae synthesized arylsulfatase mRNA only during embryonic inversion. These experiments demonstrate the usefulness of both the arylsulfatase and the sexual pheromone reporter genes. In addition, the highly regulated arylsulfatase promoter allows the construction of inducible expression vectors for cloned genes.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftProc. Nati. Acad. Sci. USA (PNAS)
Verlag:National Academy of Sciences
Band:91
Nummer des Zeitschriftenheftes oder des Kapitels:24
Seitenbereich:S. 11562-11566
Datum1994
InstitutionenBiologie und Vorklinische Medizin > Institut für Biochemie, Genetik und Mikrobiologie > Entpflichtet bzw. im Ruhestand > Prof. Dr. Manfred Sumper
Identifikationsnummer
WertTyp
271968PubMed-ID
Klassifikation
NotationArt
Algae, Green/geneticsMESH
Arylsulfatases/geneticsMESH
Base SequenceMESH
DNA Primers/chemistryMESH
Gene ExpressionMESH
Genes, ReporterMESH
Molecular Sequence DataMESH
Pheromones/geneticsMESH
Polymerase Chain ReactionMESH
Promoter Regions, GeneticMESH
RNA, Messenger/geneticsMESH
RNA, Plant/geneticsMESH
Recombinant Fusion ProteinsMESH
Restriction MappingMESH
Transformation, GeneticMESH
Dewey-Dezimal-Klassifikation500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetUnbekannt / Keine Angabe
An der Universität Regensburg entstandenUnbekannt / Keine Angabe
URN der UB Regensburgurn:nbn:de:bvb:355-epub-186784
Dokumenten-ID18678

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