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Ramakrishnan, M.

Publications and source records attributed to Ramakrishnan, M..

2 recordsLinked to original sources

Diverse phenotypic responses and phosphate content in foxtail millet genotypes under greenhouse and field conditions

Phosphorous (P) is an important macronutrient for the growth of all agricultural crops. This study reports phenotype analysis for P responses in field (two different seasons, monsoon and summer) and greenhouse, using 54 genotypes of foxtail millet (Setaria italica) under P-fertilized (P+) and unfertilized (P-) conditions. Variation was seen for plant height, leaf number and length, tillering ability and seed yield traits. Genotypes ISe 1234 and ISe 1541 were P+ responders, and the genotypes ISe 1181, ISe 1655, ISe 783 and ISe 1892 tend more towards low P tolerance for total seed yield. Genotypes that performed well under P-conditions were almost as productive as genotypes that performed well under P+ conditions suggesting some genotypes are well adapted to nutrient-poor soils. In the greenhouse, significant variation was seen for root hair density and root hair number and for fresh and dry weights of shoot and root under P-stress. However, there was not much difference in the shoot and root total P and inorganic phosphate (Pi) levels of five selected high and low responding genotypes. In the root and leaf tissues, total P and Pi contents of five high responding genotypes were higher than the five low responding genotypes.\n\nHighlightEnormous phenotypic and phosphate content variation of foxtail millet under low-phosphate supply in greenhouse and natural field conditions identifies genotypic plasticity for future breeding for improved P use efficiency.

plant biology↗

Thymidylate synthase maintains the de-differentiated state of aggressive breast cancers

Cancer cells frequently boost nucleotide metabolism (NM) to support their increased proliferation, but the consequences of elevated NM on tumor de-differentiation are mostly unexplored. Here, we identified a role for thymidylate synthase (TS), a NM enzyme and established drug target, in cancer cell de-differentiation and investigated its clinical significance in breast cancer (BC). In vitro, TS knockdown increased the population of CD24+ differentiated cells, and attenuated migration and sphere-formation. RNA-seq profiling indicated a repression of epithelial-to-mesenchymal transition (EMT) signature genes upon TS knockdown, and TS-deficient cells showed an increased ability to invade and metastasize in vivo, consistent with the occurrence of a partial EMT phenotype. Mechanistically, TS enzymatic activity was found essential for the maintenance of the EMT/stem-like state by fueling a DPYD-dependent pyrimidine catabolism. In patient tissues, TS levels were found significantly higher in poorly differentiated and in triple negative BC (TNBC), and strongly correlated with worse prognosis. The present study provides the rationale to study in-depth the role of NM at the crossroads of proliferation and differentiation, and depicts new avenues for the design of novel drug combinations for the treatment of BC.

cancer biology↗