| Literature DB >> 32327559 |
Julian Chollet1, Alexander Dünkler1, Anne Bäuerle1, Laura Vivero-Pol1, Medhanie A Mulaw2, Thomas Gronemeyer1, Nils Johnsson3.
Abstract
Yeast cells select the position of their new bud at the beginning of each cell cycle. The recruitment of septins to this prospective bud site is one of the critical events in a complex assembly pathway that culminates in the outgrowth of a new daughter cell. During recruitment, septin rods follow the high concentration of Cdc42GTP that is generated by the focused localization of the Cdc42 guanine-nucleotide-exchange factor Cdc24. We show that, shortly before budding, Cdc24 not only activates Cdc42 but also transiently interacts with Cdc11, the septin subunit that caps both ends of the septin rods. Mutations in Cdc24 that reduce affinity to Cdc11 impair septin recruitment and decrease the stability of the polarity patch. The interaction between septins and Cdc24 thus reinforces bud assembly at sites where septin structures are formed. Once the septins polymerize to form the septin ring, Cdc24 is found at the cortex of the bud and directs further outgrowth from this position.Entities:
Keywords: Cdc42; Cell polarity; Positive feedback; Protein–protein interaction; SPLIFF; Split-ubiquitin; Yeast
Mesh:
Substances:
Year: 2020 PMID: 32327559 DOI: 10.1242/jcs.240283
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285