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Rattanawong, K.

Publications and source records attributed to Rattanawong, K..

2 recordsLinked to original sources

TALE-independent transcriptional activation of the rice executor gene Xa23 is regulated via histone acetylation during zygote development

Transcription activator-like effectors (TALEs) from Xanthomonas activate transcription of executor (E) genes in host plants, leading to cell death and thereby restricting proliferation of biotrophic pathogens. Because E gene transcripts had only been detected upon activation by cognate Xanthomonas TALEs, E genes were thought to function exclusively in plant immunity. Here, we detect TALE-independent transcription of the rice E gene Xa23 in zygotes 4-6 hours after gamete fusion. Histone deacetylase inhibition induces Xa23 transcription in unfertilized egg cells, implicating histone acetylation in Xa23 regulation. We identified potential cis-regulatory elements and transcription start sites associated with native Xa23 transcription during zygote development. Together, our findings suggest that Xa23 is a developmentally regulated gene with a native role during early zygote development. This supports a previously proposed model in which E genes have native functions in development, while fortuitous upstream polymorphisms can create TALE-binding sites that convert them into immune executors.

plant biology↗

Autonomous development and regeneration of isolated rice egg cells in a fertilization-independent manner

Parthenogenesis is suppressed in rice egg cells to avoid precocious development before fertilization. We found that cold treatment released cell cycle arrest in egg cells and triggered mitosis. Egg cells isolated from japonica (Nipponbare; NB) and aus (Kasalath; KS) subspecies divided and regenerated into mature plants after cold treatment. The egg-derived plants showed variety of ploidy levels, including haploid (n), diploid (2n), and tetraploid (4n). Nuclear DNA quantification showed that genome duplication occurred during early parthenogenetic development. Owing to the presence of single nucleotide polymorphisms (SNPs) between NB and KS, inter-subspecific hybrid plants (NB-KS hybrids) were created via electrofusion. Egg cells from the NB-KS hybrid developed parthenogenetically into polyploid plants. 2n and 4n plants originating from the same NB-KS egg cell displayed the same homozygous SNP patterns throughout the genome, indicating that these plants were doubled and quadrupled haploids. Transcriptome analyses of cold-treated egg cells demonstrated that parthenogenesis-related candidate genes, including OsBBML1, were upregulated.

plant biology↗