1. Membrane organization and cell fusion during mating in fission yeast requires multipass membrane protein Prm1
- Author
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Marta Hoya, Eduardo Calpena, Janet Leatherwood, Nagore de León, Mirza Mohammad Reza Sharifmoghadam, Cristina Doncel, M. Ángeles Curto, M.-Henar Valdivieso, Comisión Interministerial de Ciencia y Tecnología, CICYT (España), Ministerio de Ciencia e Innovación (España), and Consejo Superior de Investigaciones Científicas (España)
- Subjects
Lysis ,Miconazole ,Investigations ,Models, Biological ,Cell membrane ,Fatty Acids, Monounsaturated ,Cell Wall ,Depsipeptides ,Gene Expression Regulation, Fungal ,Schizosaccharomyces ,Genetics ,medicine ,Cell fusion ,Mating ,biology ,Cell Membrane ,Membrane ,Membrane Proteins ,biology.organism_classification ,Yeast ,Cell biology ,medicine.anatomical_structure ,Membrane protein ,Cytoplasm ,Schizosaccharomyces pombe ,Prm1 ,Schizosaccharomyces pombe Proteins - Abstract
The involvement of Schizosaccharomyces pombe prm1+ in cell fusion during mating and its relationship with other genes required for this process have been addressed. S. pombe prm1Δ mutant exhibits an almost complete blockade in cell fusion and an abnormal distribution of the plasma membrane and cell wall in the area of cell-cell interaction. The distribution of cellular envelopes is similar to that described for mutants devoid of the Fig1-related claudin-like Dni proteins; however, prm1+ and the dni+ genes act in different subpathways. Time-lapse analyses show that in the wild-type S. pombe strain, the distribution of phosphatidylserine in the cytoplasmic leaflet of the plasma membrane undergoes some modification before an opening is observed in the cross wall at the cell- cell contact region. In the prm1Δ mutant, this membrane modification does not take place, and the cross wall between the mating partners is not extensively degraded; plasma membrane forms invaginations and fingers that sometimes collapse/retract and that are sometimes strengthened by the synthesis of cell-wall material. Neither prm1Δ nor prm1Δ dniΔ zygotes lyse after cell-cell contact in medium containing and lacking calcium. Response to drugs that inhibit lipid synthesis or interfere with lipids is different in wild-type, prm1Δ, and dni1Δ strains, suggesting that membrane structure/organization/dynamics is different in all these strains and that Prm1p and the Dni proteins exert some functions required to guarantee correct membrane organization that are critical for cell fusion. © 2014 by the Genetics Society of America., Financial support to H.V.M. from the Comisión Interministerial de Ciencia Y Tecnología (Spain)/European Union Fondo Europeo de Desarrollo Regional program (grant BFU2010-15085) made this work possible. M.A.C. and N.d.L were supported by Formación de Personal Universitario fellowships from the Ministry of Science, and M.H. was supported by a Junta de Ampliación de Estudios predoctoral fellowship from the Consejo Superior de Investigaciones Científicas, Spain.
- Published
- 2014