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Lima, R. B.

Publications and source records attributed to Lima, R. B..

2 recordsLinked to original sources

The dandelion PARTHENOGENESIS gene dominantly modifies Arabidopsis fertilization and embryogenesis

Parthenogenesis of totipotent egg cells is rare, yet widespread, across the tree of life but mechanistic insights into factors that control parthenogenesis remain sparse. The Taraxacum officinale PARTHENOGENESIS (ToPAR) gene encodes a C2H2-zinc finger and EAR domain containing protein which is required for parthenogenesis and clonal seed production in apomictic dandelions. Ectopic expression of ToPAR can trigger egg cell division in lettuce and maternal haploid induction in foxtail millet, and ToPAR has been employed in a high-penetrance synthetic apomixis system in hybrid rice. To date a convenient model system to study ToPAR function has yet to be established nor has the capacity for ToPAR to trigger cell division in non-gametic cells been tested. Here, we demonstrate that expression of ToPAR in egg cells of Arabidopsis thaliana using the EGG-CELL 1.1 promoter (pAtEC1.1) causes a reduction in seed set and can trigger egg cell division without fertilization. We found that the pAtEC1.1:ToPAR transgene is rarely transmitted through the female lineage where it causes aberrant cell divisions. Expression of ToPAR in sexual embryos under the WUSCHEL RELATED HOMEOBOX 8 (AtWOX8) promoter alters cell patterning disrupting morphogenesis. Our results demonstrate that A. thaliana can be a powerful system to dissect the mode of action of ToPAR, and that gamete-specific co-factors are not essential for its function.

plant biology↗

Seed coat formation in Arabidopsis requires a concerted action of JUMONJI histone H3K27me3 demethylases and Brassinosteroid signaling

Seed development in angiosperms starts with double fertilization, where two paternal sperm cells fertilize the maternal gametes. This leads to the formation of the embryo and of the endosperm. These fertilization products are enveloped by the maternally-derived seed coat, the development of which is inhibited prior to fertilization by the Polycomb Repressive Complex 2 (PRC2). This complex deposits the repressive histone mark H3K27me3, whose removal is necessary for seed coat formation. Here, we show that JUMONJI-type (JMJ) histone demethylases are expressed in the seed coats of Arabidopsis thaliana (Arabidopsis) and are necessary for its formation. We propose that JMJ activity is coupled to Brassinosteroid (BR) function, as BR effectors physically recruit JMJ proteins to target loci. Consistent with this, we show that loss of BR biosynthesis and signaling leads to seed coat defects, and that loss of the main BR receptor, BRI1, results in H3K27me3 hypermethylation. Moreover, our data points to BRI1 mediating H3K27me3 removal independently of BRs, while a different receptor, BRL3, likely regulates seed coat formation in a BR-dependent manner. We thus propose a model where seed coat development relies on canonical and non-canonical functions of BR receptors.

plant biology↗