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Reference - PMID:28410370 - A systematic screen for morphological abnormalities during fission yeast sexual reproduction identifies a mechanism of actin aster formation for cell fusion.

Reference summary

PubMed ID
PMID:28410370
Title
A systematic screen for morphological abnormalities during fission yeast sexual reproduction identifies a mechanism of actin aster formation for cell fusion.
Authors
Dudin O, Merlini L, Bendezú FO, Groux R, Vincenzetti V, Martin SG
Citation
PLoS Genet 2017 Apr;13(4):e1006721
Publication year
2017
Abstract
In non-motile fungi, sexual reproduction relies on strong morphogenetic changes in response to pheromone signaling. We report here on a systematic screen for morphological abnormalities of the mating process in fission yeast Schizosaccharomyces pombe. We derived a homothallic (self-fertile) collection of viable deletions, which, upon visual screening, revealed a plethora of phenotypes affecting all stages of the mating process, including cell polarization, cell fusion and sporulation. Cell fusion relies on the formation of the fusion focus, an aster-like F-actin structure that is marked by strong local accumulation of the myosin V Myo52, which concentrates secretion at the fusion site. A secondary screen for fusion-defective mutants identified the myosin V Myo51-associated coiled-coil proteins Rng8 and Rng9 as critical for the coalescence of the fusion focus. Indeed, rng8Δ and rng9Δ mutant cells exhibit multiple stable dots at the cell-cell contact site, instead of the single focus observed in wildtype. Rng8 and Rng9 accumulate on the fusion focus, dependent on Myo51 and tropomyosin Cdc8. A tropomyosin mutant allele, which compromises Rng8/9 localization but not actin binding, similarly leads to multiple stable dots instead of a single focus. By contrast, myo51 deletion does not strongly affect fusion focus coalescence. We propose that focusing of the actin filaments in the fusion aster primarily relies on Rng8/9-dependent cross-linking of tropomyosin-actin filaments.

Annotation

GO biological process

GO:0000747 - conjugation with cellular fusion

Genes:

GO:0000755 - cytogamy

Genes:

GO:1904600 - mating projection actin fusion focus assembly

Genes:

GO cellular component

GO:1990819 - mating projection actin fusion focus

Genes:

GO:0070250 - mating projection membrane

Genes:

GO:0043332 - mating projection tip

Genes:

Single locus phenotype

FYPO:0006108 - abnormal actin fusion focus assembly

Genes:

Genotypes:

FYPO:0006503 - abnormal protein localization to actin fusion focus

Genes:

Genotypes:

FYPO:0000357 - abnormal shmoo morphology

Genes:

Genotypes:

FYPO:0000121 - abnormal sporulation

Genes:

Genotypes:

FYPO:0003066 - abnormal sporulation resulting in formation of ascus with fewer than four spores

Genes:

Genotypes:

FYPO:0000413 - abolished cell fusion during mating

Genes:

Genotypes:

FYPO:0006010 - abolished shmoo contact with partner cell

Genes:

Genotypes:

FYPO:0002488 - cell lysis

Genes:

Genotypes:

FYPO:0000708 - decreased mating efficiency

Genes:

Genotypes:

FYPO:0007096 - decreased protein localization to actin fusion focus

Genes:

Genotypes:

FYPO:0002869 - decreased protein localization to cell division site

Genes:

Genotypes:

FYPO:0000587 - delayed onset of sporulation

Genes:

Genotypes:

FYPO:0006012 - elongated cell with abolished shmoo formation

Genes:

Genotypes:

FYPO:0004806 - incomplete cell wall disassembly at cell fusion site

Genes:

Genotypes:

FYPO:0006013 - large ascus

Genes:

Genotypes:

FYPO:0004295 - multiseptate cell

Genes:

Genotypes:

FYPO:0006015 - multiseptate cell with shmoo

Genes:

Genotypes:

FYPO:0006014 - promiscuous mating

Genes:

Genotypes:

FYPO:0006011 - shmoo formation at cell side

Genes:

Genotypes:

FYPO:0000022 - shmoo with long tip

Genes:

Genotypes:

FYPO:0007683 - wide actin fusion focus

Genes:

Genotypes: