Control of daughter cell fates during asymmetric division: interaction of Numb and Notch.
During development of the Drosophila peripheral nervous system, a sensory organ precursor (SOP) cell undergoes rounds of asymmetric divisions to generate four distinct cells of a sensory organ. Numb, a membrane-associated protein, is asymmetrically segregated into one daughter cell during SOP division and acts as an inherited determinant of cell ... fate. Here, we show that Notch, a transmembrane receptor mediated cell-cell communication, functions as a binary switch in cell fate specification during asymmetric divisions of the SOP and its daughter cells in embryogenesis. Moreover, numb negatively regulates Notch, probably through direct protein-protein interaction that requires the phosphotyrosine-binding (PTB) domain of Numb and either the RAM23 region or the very C-terminal end of Notch. Notch then positively regulates a transcription factor encoded by tramtrack (ttk). This leads to Ttk expression in the daughter cell that does not inherit Numb. Thus, the inherited determinant Numb bestows a bias in the machinery for cell-cell communication to allow the specification of distinct daughter cell fates.
Mesh Terms:
Animals, Cell Differentiation, Cell Line, Drosophila, Drosophila Proteins, Embryonic and Fetal Development, Female, Juvenile Hormones, Male, Membrane Proteins, Receptors, Notch, Sense Organs, Stem Cells, Transcription Factors
Animals, Cell Differentiation, Cell Line, Drosophila, Drosophila Proteins, Embryonic and Fetal Development, Female, Juvenile Hormones, Male, Membrane Proteins, Receptors, Notch, Sense Organs, Stem Cells, Transcription Factors
Neuron
Date: Jul. 01, 1996
PubMed ID: 8755476
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