Abstract

Since the discovery of double fertilization, it has been recognized that flowering plants produce two highly dimorphic female gametes, the egg cell and central cell. These give rise, respectively, to the embryo and the endosperm, a nourishing tissue unique to flowering plants. Here we show that in Arabidopsis, endosperm formation requires the CYTOKININ INDEPENDENT 1 (CKI1) histidine kinase, an activator of the cytokinin signaling pathway, which specifies central cells and restricts egg cell fate. Dimorphism of the two adjacent gametes is mechanistically established in the syncytial embryo sac by spatially restricted CKI1 expression, followed by translocation of ER-localized CKI1 protein via nuclear migration. Cell specification by CKI1 likely involves activation of the cytokinin signaling pathway mediated by histidine phosphotransferases. Ectopic CKI1 expression generates non-propagating seeds with dual fertilized endosperms and no embryos. We conclude that CKI1-directed specification of the endosperm precursor central cell results in seeds containing an embryo and an endosperm.

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