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  Cell fate specification by even-skipped expression in the Drosophila nervous system is coupled to cell cycle progression

Weigmann, K., & Lehner, C. (1995). Cell fate specification by even-skipped expression in the Drosophila nervous system is coupled to cell cycle progression. Development, 121(11), 3713-3721. doi:10.1242/dev.121.11.3713.

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Weigmann, K1, Autor           
Lehner, CF1, Autor           
Affiliations:
1Lehner Group, Friedrich Miescher Laboratory, Max Planck Society, ou_3400347              

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 Zusammenfassung: The correct specification of defined neurons in the Drosophila central nervous system is dependent on even-skipped. During CNS development, even-skipped expression starts in the ganglion mother cell resulting from the first asymmetric division of neuroblast NB 1-1. This first division of NB 1-1 (and of the other early neuroblasts as well) is temporally controlled by the transcriptional regulation of string expression, which we have manipulated experimentally, even-skipped expression still occurs if the first neuroblast division is delayed, but not if the division is prohibited. Moreover, even-skipped expression is also dependent on progression through S phase which follows immediately after the first division. However, cytokinesis during the first NB division is not required for even-skipped expression as revealed by observations in pebble mutant embryos. Our results demonstrate therefore that even-skipped expression is coupled to cell cycle progression, presumably in order to prevent a premature activation of expression by a positive regulator which is produced already in the neuroblast during G2 and segregated asymmetrically into the ganglion mother cell during mitosis.

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 Datum: 1995-11
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1242/dev.121.11.3713
PMID: 8582283
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Titel: Development
  Andere : Development
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Cambridgeshire : Company of Biologists
Seiten: - Band / Heft: 121 (11) Artikelnummer: - Start- / Endseite: 3713 - 3721 Identifikator: ISSN: 0950-1991
CoNE: https://pure.mpg.de/cone/journals/resource/954927546241