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Garcia, M. S.

Publications and source records attributed to Garcia, M. S..

2 recordsLinked to original sources

Genomic regions of durum wheat involved in water productivity.

Durum wheat is a staple food of the Mediterranean Basin, mostly cultivated under rainfed conditions. As such, the crop is often exposed to moisture stress. Therefore, the identification of genetic factors controlling the capacity of genotypes to convert moisture into grain yield (i.e. water productivity) is quintessential to stabilize production despite climatic variations. A global panel of 384 accessions was tested across eighteen Mediterranean environments (Morocco, Lebanon, and Jordan) representing a vast range of moisture levels. The accessions were assigned to water responsiveness classes, with genotypes Responsive to Low Moisture reaching an average + 1.5 kg ha-1 mm-1 advantage. Genome wide association studies (GWAS) revealed that six loci explained the majority of this variation. A second validation panel tested under moisture stress confirmed that carrying the positive allele at three loci on chromosomes 1B, 2A and 7B generated an average water productivity gain of + 2.2 kg ha-1 mm-1. Interestingly, loci on chromosome 2A is novel. The three loci were tagged by Kompetitive Allele Specific PCR (KASP) markers, and these were used to screen a third independent validation panel composed by elites tested across moisture stressed sites. The three KASP combined predicted up to 34% of the variation for grain yield at 65% accuracy. These loci are now ready for molecular pyramiding and transfer across cultivars to improve the moisture conversion of durum wheat. HighlightLoci controlling drought tolerance were identified using a solid strategy, involving 3 different panels. Those loci associated enables higher water productivity and grain yield.

plant biology↗

Bumetanide increases microglia-interneuron contact following traumatic brain injury

ObjectiveThe Na-K-Cl cotransporter (NKCC1) inhibitor bumetanide has prominent positive effects on the pathophysiology of many neurological disorders. Here we studied whether bumetanide could influence post-traumatic cognitive decline and inflammatory processes by regulating astrocyte and microglia activation. MethodControlled cortical impacted (CCI) animals were treated with bumetanide during the first post-CCI week. Immunochemistry, flow cytometry, immunoassay, and in vivo imaging were used to study astrocytic and microglial morphology and phenotype as well as adult neurogenesis. Telemetric electroencephalograms and cognitive behavioral test were performed at one-month post CCI. ResultsBumetanide prevented CCI-induced decrease in hippocampal neurogenesis and parvalbumin positive interneuron loss. Deletion of NKCC1 in astrocytes neither rescued interneurons nor promote neurogenesis. Interestingly, bumetanide had a strong effect on microglial activation by inducing polarization towards the M1-like phenotype 3 days post-CCI and the M2-like phenotype 7 days post-CCI. Bumetanide increased microglial Brain-derived neurotrophic factor (BDNF) expression and interaction with parvalbumin interneurons. The early treatment with bumetanide resulted in improvements in working and episodic memory, one-month post-CCI, as well as the normalization of theta band oscillations. InterpretationHere, we disclose a novel mechanism for the neuroprotective action of bumetanide mediated by an acceleration of microglial activation dynamics that leads to an increase of parvalbumin interneuron survival following CCI, possibly resulting from increased microglial BDNF expression and contact with interneurons. Salvage of interneurons may normalize ambient gamma-aminobutyric acid (GABA) resulting in the preservation of adult neurogenesis processes as well as contributing to bumetanide-mediated improvement of cognitive performance.

neuroscience↗