INCREASED SIZE EXCLUSION LIMIT2 Encodes a Putative DEVH Box RNA Helicase Involved in Plasmodesmata Function during Arabidopsis Embryogenesis
INCREASED SIZE EXCLUSION LIMIT2 Encodes a Putative DEVH Box RNA Helicase Involved in Plasmodesmata Function during Arabidopsis Embryogenesis
Abstract Here, we characterize the Arabidopsis thaliana embryo-defective mutant increased size exclusion limit2 (ise2). In contrast with wild-type embryos, ise2 mutants continue to traffic 10-kD fluorescent dextran in the mid-torpedo stage of development. ise2 embryos contain branched as well as simple plasmodesmata (PD) compared with wild-type embryos, which only contain simple PD. Positional cloning reveals that the ISE2 gene encodes a putative DEVH box RNA helicase that shares sequence homology with RNA helicases involved in RNA degradation pathways in other organisms. ISE2 localizes to granule-like structures in the cytoplasm. These granules increase in number when plant cells are stressed. These features are characteristic of stress granules (SGs) in mammalian cells, suggesting that ISE2 granules represent plant-specific SGs. Genetic data demonstrate that the ISE2 helicase is involved in posttranscriptional gene silencing and the determination of cell fate. These data together suggest that ISE2 function affects PD structure and function through the regulation of RNA metabolism and consequent gene expression.
- University of California, Berkeley United States
- University of Wisconsin–Oshkosh United States
- Stanford University United States
- University of Wisconsin–Madison United States
Arabidopsis Proteins, Secretory Vesicles, Arabidopsis, Plasmodesmata, Chromosome Mapping, Down-Regulation, Embryonic Development, Biological Transport, Dextrans, MicroRNAs, Protein Transport, Phenotype, Seedlings, Mutation, Gene Silencing, RNA, Messenger, Cloning, Molecular, Cotyledon, Biomarkers, RNA Helicases
Arabidopsis Proteins, Secretory Vesicles, Arabidopsis, Plasmodesmata, Chromosome Mapping, Down-Regulation, Embryonic Development, Biological Transport, Dextrans, MicroRNAs, Protein Transport, Phenotype, Seedlings, Mutation, Gene Silencing, RNA, Messenger, Cloning, Molecular, Cotyledon, Biomarkers, RNA Helicases
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