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Structure and expression of the murine Sp100 nuclear dot gene

Dieter Weichenhan*, Bärbel Kunze, Stefan Zacker, Walther Traut, Heinz Winking

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

The human SP100 gene encodes an autoantigen that colocalizes with two other proteins, PML and NDP52, in distinct nuclear domains, called 'nuclear dots' (NDs). NDs do not overlap with other known subnuclear structures, and their function is still unknown. Patients suffering from the autoimmune disease primary biliary cirrhosis often produce antibodies against the SP100 protein. The present study describes the structure and expression of the murine Sp100 gene. In the species Mus caroli, Sp100 consists of 17 exons that are distributed over a range of 52 kb. The human and murine Sp100 promoters are very similar, and both harbor an interferon-stimulated response element. Like its human counterpart, the murine Sp100 gene is responsive to interferon treatment. The house mouse, Mus musculus, harbors the Sp100 gene and a second gene with homology to Sp100, the multicopy Sp100-rs gene. However, in contrast to the genuine mouse homolog, Sp100-rs shares only segmental homology with the human Sp100 gene. Replacement of the murine Sp100 gene by a defective copy is now feasible and should shed light on its function in an animal model.

OriginalspracheEnglisch
ZeitschriftGenomics
Jahrgang43
Ausgabenummer3
Seiten (von - bis)298-306
Seitenumfang9
ISSN0888-7543
DOIs
PublikationsstatusVeröffentlicht - 01.08.1997

Fördermittel

The technical assistance of Katja Andruleit, Petra Nielsen, and Stefanie Schwindt is gratefully acknowledged. We thank Thomas Hellwig for his help in the quantitation of blot signals. This work was supported by the Deutsche Forschungsgemeinschaft.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

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