Villin Controls the Formation and Enlargement of Punctate Actin Foci in Pollen Tubes

Author:

Zhao Wanying1,Qu Xiaolu12,Zhuang Yuhui1,Wang Ludi3,Bosch Maurice3ORCID,Franklin-Tong Vernonica E.4ORCID,Xue Yongbiao56ORCID,Huang Shanjin1ORCID

Affiliation:

1. Center for Plant Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China

2. Key Laboratory of Horticultural Plant Biology (Ministry of Education), College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China

3. Institute of Biological, Environmental and Rural Sciences (IBERS), Aberystwyth University, Plas Gogerddan, Aberystwyth, SY23 3EE, UK

4. School of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK

5. State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China

6. Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China

Abstract

Self-incompatibility (SI) in Papaver rhoeas triggers dramatic actin alterations in pollen. However, how actin alterations in SI pollen tubes are mechanistically achieved remains largely unexplored. Here we have used treatment with the calcium ionophore A23187 to mimic the SI-induced elevation in cytosolic Ca2+ and trigger the formation of the distinctive F-actin foci. Live-cell imaging reveals that this remodeling involves F-actin fragmentation and depolymerization, accompanied by the rapid formation of punctate actin foci and subsequent increase in their size. We establish that actin foci are generated and enlarged from crosslinking of fragmented actin filament structures. Moreover, we show that villins associate with actin structures and are involved in this actin reorganization process. Notably, we demonstrate that Arabidopsis villin5 promotes actin depolymerization and formation of actin foci by fragmenting actin filaments, and controlling the enlargement of actin foci via bundling actin filaments. Our study thus uncovers important, novel insights about the molecular players and mechanisms involved in forming the distinctive actin foci in pollen tubes.

Funder

National Natural Science Foundation of China

the Biotechnology and Biological Sciences Research Council

Publisher

The Company of Biologists

Subject

Cell Biology

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