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The Arp2/3 complex and the formin, Diaphanous, are both required to regulate the size of germline ring canals in the developing egg chamber.

Authors :
Thestrup, Josephine
Tipold, Marina
Kindred, Alexandra
Stark, Kara
Curry, Travis
Lewellyn, Lindsay
Source :
Developmental Biology. May2020, Vol. 461 Issue 1, p75-85. 11p.
Publication Year :
2020

Abstract

Intercellular bridges are an essential structural feature found in both germline and somatic cells throughout the animal kingdom. Because of their large size, the germline intercellular bridges, or ring canals, in the developing fruit fly egg chamber are an excellent model to study the formation, stabilization, and growth of these structures. Within the egg chamber, the germline ring canals connect 15 supporting nurse cells to the developing oocyte, facilitating the transfer of materials required for successful oogenesis. The ring canals are derived from a stalled actomyosin contractile ring; once formed, additional actin and actin-binding proteins are recruited to the ring to support the 20-fold growth that accompanies oogenesis. These behaviors provide a unique model system to study the actin regulators that control incomplete cytokinesis, intercellular bridge formation, and growth. By temporally controlling their expression in the germline, we have demonstrated that the Arp2/3 complex and the formin, Diaphanous (Dia), coordinately regulate ring canal size and growth throughout oogenesis. Dia is required for successful incomplete cytokinesis and the initial stabilization of the germline ring canals. Once ring canals have formed, the Arp2/3 complex and Dia cooperate to determine ring canal size and maintain stability. Our data suggest that nurse cells must maintain a precise balance between the activity of these two nucleators during oogenesis. Image 1 • Depletion of ArpC2 leads to variation in ring canal size throughout oogenesis. • Diaphanous is required for incomplete cytokinesis and to limit ring canal expansion. • Expression of an activated Diaphanous produces smaller, lumenless ring canals. • Reducing Diaphanous provides a modest rescue of the arpC2-RNAi phenotype. • Once formed, the Arp2/3 complex and Diaphanous coordinately regulate ring canal size. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00121606
Volume :
461
Issue :
1
Database :
Academic Search Index
Journal :
Developmental Biology
Publication Type :
Academic Journal
Accession number :
142734981
Full Text :
https://doi.org/10.1016/j.ydbio.2020.01.007