Behavior of Male Gamete Fusogen GCS1/HAP2 and the Regulation in Arabidopsis Double Fertilization

Author:

Shiba Yuka1,Takahashi Taro1,Ohashi Yukino1,Ueda Minako23,Mimuro Amane1,Sugimoto Jin1,Noguchi Yuka1,Igawa Tomoko14ORCID

Affiliation:

1. Graduate School of Horticulture, Chiba University, Matsudo 648, Matsudo-shi 271-8510, Japan

2. Graduate School of Life Sciences, Department of Ecological Developmental Adaptability Life Sciences, Tohoku University, 2-1-1 Katahira, Sendai 980-8577, Japan

3. Suntory Rising Stars Encouragement Program in Life Sciences (SunRiSE), Sendai 980-8578, Japan

4. Plant Molecular Science Center, Chiba University, 1-33 Yayoi, Chiba-shi 263-8522, Japan

Abstract

In the sexual reproduction of flowering plants, two independent fertilization events occur almost simultaneously: two identical sperm cells fuse with either the egg cell or the central cell, resulting in embryo and endosperm development to produce a seed. GCS1/HAP2 is a sperm cell membrane protein essential for plasma membrane fusion with both female gametes. Other sperm membrane proteins, DMP8 and DMP9, are more important for egg cell fertilization than that of the central cell, suggesting its regulatory mechanism in GCS1/HAP2-driving gamete membrane fusion. To assess the GCS1/HAP2 regulatory cascade in the double fertilization system of flowering plants, we produced Arabidopsis transgenic lines expressing different GCS1/HAP2 variants and evaluated the fertilization in vivo. The fertilization pattern observed in GCS1_RNAi transgenic plants implied that sperm cells over the amount of GCS1/HAP2 required for fusion on their surface could facilitate membrane fusion with both female gametes. The cytological analysis of the dmp8dmp9 sperm cell arrested alone in an embryo sac supported GCS1/HAP2 distribution on the sperm surface. Furthermore, the fertilization failures with both female gametes were caused by GCS1/HAP2 secretion from the egg cell. These results provided a possible scenario of GCS1/HAP2 regulation, showing a potential scheme for capturing additional GCS1/HAP2-interacting proteins.

Funder

Japan Society for the Promotion of Science KAKENHI

NAGASE Science Technology Foundation

Strategic Priority Research Promotion on Phytochemical Plant Molecular Sciences, Chiba University

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry

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