Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT

Freigegeben

Zeitschriftenartikel

The three rows gene of Drosophila melanogaster encodes a novel protein that is required for chromosome disjunction during mitosis

MPG-Autoren
/persons/resource/persons282617

Stratmann,  R
Lehner Group, Friedrich Miescher Laboratory, Max Planck Society;

/persons/resource/persons277069

Lehner,  CF
Lehner Group, Friedrich Miescher Laboratory, Max Planck Society;

Externe Ressourcen
Es sind keine externen Ressourcen hinterlegt
Volltexte (beschränkter Zugriff)
Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.
Volltexte (frei zugänglich)
Es sind keine frei zugänglichen Volltexte in PuRe verfügbar
Ergänzendes Material (frei zugänglich)
Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar
Zitation

D'Andrea, R., Stratmann, R., Lehner, C., John, U., & Saint, R. (1993). The three rows gene of Drosophila melanogaster encodes a novel protein that is required for chromosome disjunction during mitosis. Molecular Biology of the Cell, 4(11), 1161-1174. doi:10.1091/mbc.4.11.1161.


Zitierlink: https://hdl.handle.net/21.11116/0000-000D-1B34-B
Zusammenfassung
Zygotic expression of the three rows (thr) gene of Drosophila melanogaster is required for normal cell proliferation during embryogenesis. Mitotic defects in thr mutant embryos begin during mitosis 15, and all subsequent divisions are disrupted. Chromosome disjunction and consequently cytokinesis fail during these defective mitoses, although the initial mitotic processes (chromosome condensation, spindle assembly, metaphase plate formation, and cyclin degradation) are not affected. Despite the failure of chromosome disjunction and cytokinesis, later mitotic events (chromosome decondensation) and subsequent cell cycle progression continue. The thr gene has been isolated and shown to encode a 1209 amino acid protein that shares no extended sequence similarity with known proteins. thr mRNA is present as maternal mRNA that degrades at the time of cellularization. At this and all subsequent times during embryogenesis, zygotic expression correlates with mitotic proliferation. These observations, together with the observation that the zygotic phenotype of thr mutant embryos is influenced by the maternal genotype, suggest that the embryonic phenotype results from exhaustion of the maternal thr contribution and does not reflect a developmentally restricted requirement for thr function. Our results indicate that the novel thr product is required specifically for chromosome disjunction during all mitoses.