Cooperation between Paxillin-like Protein Pxl1 and Glucan Synthase Bgs1 Is Essential for Actomyosin Ring Stability and Septum Formation in Fission Yeast

Author

Pujol Carrión, Núria

Sato, Mamiko

Pinar, Mario

Ramos, Mariona

Moreno, Belén

Osumi, Masako

Ribas, Juan Carlos

Pérez, Pilar

Cortés, Juan C. G.

Publication date

2015-11-11T12:05:13Z

2015-11-11T12:05:13Z

2015



Abstract

In fungal cells cytokinesis requires coordinated closure of a contractile actomyosin ring (CAR) and synthesis of a special cell wall structure known as the division septum. Many CAR proteins have been identified and characterized, but how these molecules interact with the septum synthesis enzymes to form the septum remains unclear. Our genetic study using fission yeast shows that cooperation between the paxillin homolog Pxl1, required for ring integrity, and Bgs1, the enzyme responsible for linear β(1,3)glucan synthesis and primary septum formation, is required for stable anchorage of the CAR to the plasma membrane before septation onset, and for cleavage furrow formation. Thus, lack of Pxl1 in combination with Bgs1 depletion, causes failure of ring contraction and lateral cell wall overgrowth towards the cell lumen without septum formation. We also describe here that Pxl1 concentration at the CAR increases during cytokinesis and that this increase depends on the SH3 domain of the F-BAR protein Cdc15. In consequence, Bgs1 depletion in cells carrying a cdc15ΔSH3 allele causes ring disassembly and septation blockage, as it does in cells lacking Pxl1. On the other hand, the absence of Pxl1 is lethal when Cdc15 function isaffected, generating a large sliding of the CAR with deposition of septum wall material along the cell cortex, and suggesting additional functions for both Pxl1 and Cdc15 proteins. In conclusion, our findings indicate that CAR anchorage to the plasma membrane through Cdc15 and Pxl1, and concomitant Bgs1 activity, are necessary for CAR maintenance and septum formation in fission yeast.


This work was supported by the Spanish Ministry of Science and Innovation (BFU2010-15641 and BFU2013-39394-P) to PP. JCR was financed by the Spanish Ministry of Science and Innovation (BIO2012-35372), and Junta de Castilla y León, Spain (CSI037U14). JCGC was supported by a Juan de la Cierva postdoctoral contract from the Spanish Ministry of Science and Innovation.

Document Type

article
publishedVersion

Language

English

Publisher

Public Library of Science

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info:eu-repo/grantAgreement/MINECO//BIO2012-35372/ES/CONTROL DE LA MORFOGENESIS Y CITOCINESIS DE LA CELULA FUNGICA. HERRAMIENTAS BIOTECNOLOGICAS Y DIANAS PARA EL ESTUDIO DE ANTIFUNGICOS ESPECIFICOS/

Reproducció del document publicat a https://doi.org/10.1371/journal.pgen.1005358

PLoS Genetics, 2015, vol. 11, núm. 7

Rights

cc-by (c) G. Cortés, Juan C. et al., 2015

http://creativecommons.org/licenses/by/3.0/es/

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