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Bhat, S. R.

Publications and source records attributed to Bhat, S. R..

2 recordsLinked to original sources

Loss of Nucleotide Sugar Transporter (AtNST) gene function in the Golgi membranes impairs pollen development and embryo sac progression in Arabidopsis thaliana

O_LINucleotide Sugar Transporters (NSTs) are transmembrane proteins which are localized in the Golgi membranes and transport nucleotide sugars from cytosol to Golgi lumen. Transported nucleotide-sugars serve as donors in post-translational modification of proteins/ lipids, and donate sugar moiety to growing carbohydrate chain on nascent protein/lipid molecule, a reaction catalyzed by the enzyme glycosyltransferase. C_LIO_LIHere we reported that a mutation in the Arabidopsis thaliana gene At3g11320 coding for NST protein causes defects in male gametophyte development including collapsed, nonviable pollen. This mutation also caused impairment in the female gametophyte progression by arresting it at the functional megaspore (FM) stage. C_LIO_LIFurther, the mutant phenotype including silique size and seed set was reverted when the cDNA of AtNST gene was over-expressed in the mutant back ground. No abortive ovules were found in the siliques from the complemented plants. C_LIO_LIThe results suggest that AtNST (At3g11320) gene might be responsible for maintaining and regulating transport of nucleotide-sugars from cytoplasm to the Golgi lumen for the glycosylation of essential proteins/carbohydrates/lipids etc., which are necessary for both male and female gametophyte development stages. This study shed further light on the role of such nucleotide sugar transporters in plant reproductive development processes, at least in Arabidopsis. C_LI

plant biology↗

Impaired embryo sac cellularization by PMEI gene mutation affects gamete specification and twin plants in Arabidopsis

Arabidopsis lines with loss-of-function mutations in the gene encoding Embryo sac Pectin MethylEsterase Inhibitor (Atepmei) were found to have short silique and high seed sterility. Examination of tissue-cleared mature ovules (FG7-stage) revealed irregularly positioned nuclei within the embryo sacs. Instead of horse-shoe-shaped ovules, defective globular ovules without proper micropylar and chalazal ends were found. Embryo sac cell-type-specific GFP marker expression studies confirmed gamete and accessory cell identity alterations. Egg cell-specific marker (DD45) expression analysis confirmed the presence of multiple egg cells in the mutant embryo sacs, possibly due to defect in embryo sac cellularization. These supernumerary egg cells were functional as evident from the production of twin embryos when supernumerary sperm cells were provided. The results of Ruthenium red and tannic acid-ferric chloride staining of Atepmei mutant developing ovules, conferred its interaction with the specific PME in proper cell wall formation and maintenance around embryo sac nuclei which also coincide with its fate as a specific gamete. This is the first report implicating role of cell wall in gamete cell fate determination by altering cell-cell communication. Our analysis of the twin-embryo phenotype of epmei mutants also sheds light on the boundary conditions for double fertilization in plant reproduction.

plant biology↗