Par3 cooperates with Sanpodo for the assembly of Notch clusters following asymmetric division of <i>Drosophila</i> sensory organ precursor cells.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 34596529.
- Also identified by DOI 10.7554/eLife.66659 and PMC identifier 8516416.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
In multiple cell lineages, Delta-Notch signalling regulates cell fate decisions owing to unidirectional signalling between daughter cells. In <i>Drosophila</i> pupal sensory organ lineage, Notch regulates the intra-lineage pIIa/pIIb fate decision at cytokinesis. Notch and Delta that localise apically and basally at the pIIa-pIIb interface are expressed at low levels and their residence time at the plasma membrane is in the order of minutes. How Delta can effectively interact with Notch to trigger signalling from a large plasma membrane area remains poorly understood. Here, we report that the signalling interface possesses a unique apico-basal polarity with Par3/Bazooka localising in the form of nano-clusters at the apical and basal level. Notch is preferentially targeted to the pIIa-pIIb interface, where it co-clusters with Bazooka and its cofactor Sanpodo. Clusters whose assembly relies on Bazooka and Sanpodo activities are also positive for Neuralized, the E3 ligase required for Delta activity. We propose that the nano-clusters act as snap buttons at the new pIIa-pIIb interface to allow efficient intra-lineage signalling.
Medical subject headings
- Cell Division
- Drosophila Proteins
- Drosophila melanogaster
- Intracellular Signaling Peptides and Proteins
- Membrane Proteins
- Receptors, Notch
- Sense Organs
- Stem Cells