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Yeshvekar, R.

Publications and source records attributed to Yeshvekar, R..

2 recordsLinked to original sources

Structurally diverse calloses/β-1,3-glucans in plant cell wall microdomains

Cell walls underpin the mechanics of cell growth, intercellular signalling, and defence against pathogenic organisms. {beta}-(1,3)-glucans (also known as callose) are polysaccharides found in plants, fungi, and some bacterial species. In developing plant organs, callose accumulates around intercellular channels (plasmodesmata) controlling cell-to-cell communication. We developed monoclonal antibodies for the detection of {beta}-(1,3)-glucans and using these identified distinct populations of callose differing in size and secondary structure. Callose sub-populations were in proximal but not overlapping cell wall microdomains implying distinct spatial and functional microenvironments. We also unveiled callose interaction with xyloglucan; another plant glycan regulating cell wall functions. This work challenges previous views demonstrating structural heterogeneity in plant callose and supporting interactions between glycans with roles in the regulation of cell wall properties and functions.

plant biology↗

A mitochondria-targeted PPR protein restores cytoplasmic male sterility by post-transcriptional modification of ORF147 in Cajanus cajanifolius

Restoration factors (Rfs) belonging to the pentatricopeptide repeat proteins (PPRs) family play an essential role in plant growth and development including their binding to CMS-associated mitochondrial RNAs leading to fertility restoration. The present study identified 22 mitochondrial-specific PPRs in pigeonpea and explored the underlying mechanisms of restoration of fertility in the A4 CMS system through yeast-three hybrid studies. The identified gene was functionally validated through transgenic expression in Arabidopsis model system and obtained conclusive evidence that the identified Rf-PPR was responsible for fertility restoration. The sub-cellular localization studies implied that the identified Rf-PPR is mitochondrial targeting. The study demonstrated that due to the interaction between mitochondrial CMS mRNA and nuclear Rf-PPR protein, post-transcriptional modification occurred, leading to the inability to translate and accumulate cytotoxic CMS protein resulting in fertility restoration. The study specifically looks into the RNA-protein interaction occurring at the nucleo-cytoplasmic level in the A4 cytoplasm of Cajanus cajanifolius. HighlightsThe study identifies the restoration of fertility genes corresponding to the CMS-causing orf147 gene.

developmental biology↗