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Wani, M.

Publications and source records attributed to Wani, M..

2 recordsLinked to original sources

Steviol glycoside biosynthesis pathway gene expression profiling of transformed and non-transformed plant leaf tissues of Stevia rebaudiana (Bertoni)

Stevia rebaudiana Bertoni, a member of the Asteraceae family, is recognized for its sweetened leaves which are remarkably sweeter than sucrose by 200-300 times. This astounding property is because of steviol glycosides (SGs), a class of diterpenoid secondary metabolites which primarily consists of stevioside and rebaudioside A. These compounds are formed through a specific steviol glycoside (SG) biosynthetic pathway that contains several key genes. In the present work, gene expression profiling of 15 core genes of SG biosynthetic pathway, along with metabolite analysis were conducted in three groups of Stevia rebaudiana plants: In vitro regenerated non-transformed plantlets (NP), in vitro regenerated transformed plantlets (TP) via hairy root cultures using Rhizobium rhizogenes mediated transformation and Control plants (CP). Quantitative real-time PCR (qRT-PCR) results showed that in NP and TP there was upregulation of 13 genes. Both NP and TP showed downregulated SrDXR and SrCDPS in comparison to CP, whereas SrUGT74G1 had higher expression in NP than TP. HPLC chromatographic studies on SGs showed that stevioside content followed the order TP > NP > CP. These findings demonstrate that transformation enhances SG biosynthesis and support the use of genetically modified Stevia rebaudiana lines for increased natural sweetener production. Further studies are warranted to elucidate regulatory mechanisms and optimize metabolic engineering approaches. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/670226v1_ufig1.gif" ALT="Figure 1"> View larger version (48K): org.highwire.dtl.DTLVardef@1615c89org.highwire.dtl.DTLVardef@10264a0org.highwire.dtl.DTLVardef@1c7935org.highwire.dtl.DTLVardef@159aea3_HPS_FORMAT_FIGEXP M_FIG C_FIG

plant biology↗

Coupling metastasis to pH sensing G Protein-coupled receptor-68 through first in class inhibitor identified in an in vivo chemical genetic screen

An acidic milieu is a hallmark of the glycolytic metabolism that occurs in cancerous cells. The acidic environment is known to promote cancer progression, but the underlying signaling and cell biological underpinnings of these phenomena are not well understood. Here, we describe ogremorphin, a first-in-class small-molecule inhibitor of GPR68, an extracellular proton-sensing and mechanosensing G protein-coupled receptor. Ogremorphin was discovered in a chemical genetic zebrafish screen for its ability to perturb neural crest development, which shares basic cell behaviors of migration and invasion with cancer metastasis. Ogremorphin also inhibited migration and invasive behavior of neural crest-derived human melanoma cells in vitro. Furthermore, in phenome-wide association studies (PheWAS), we identified an aberrantly activated variant of GPR68, which is associated with cancer metastasis in vivo and promotes invasive phenotypes of cancer cells in vitro. Thus, extracellular proton-sensing GPR68 signaling promotes cell migration and invasion during embryonic development and may do likewise in cancer progression.

cancer biology↗