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1.
Sci Rep ; 12(1): 9205, 2022 06 02.
Article in English | MEDLINE | ID: mdl-35655088

ABSTRACT

The rhizosheath, the layer of soil that adheres strongly to roots, influences water and nutrients acquisition. Pearl millet is a cereal crop that plays a major role for food security in arid regions of sub-Saharan Africa and India. We previously showed that root-adhering soil mass is a heritable trait in pearl millet and that it correlates with changes in rhizosphere microbiota structure and functions. Here, we studied the correlation between root-adhering soil mass and root hair development, root architecture, and symbiosis with arbuscular mycorrhizal fungi and we analysed the genetic control of this trait using genome wide association (GWAS) combined with bulk segregant analysis and gene expression studies. Root-adhering soil mass was weakly correlated only to root hairs traits in pearl millet. Twelve QTLs for rhizosheath formation were identified by GWAS. Bulk segregant analysis on a biparental population validated five of these QTLs. Combining genetics with a comparison of global gene expression in the root tip of contrasted inbred lines revealed candidate genes that might control rhizosheath formation in pearl millet. Our study indicates that rhizosheath formation is under complex genetic control in pearl millet and suggests that it is mainly regulated by root exudation.


Subject(s)
Pennisetum , Genome-Wide Association Study , Pennisetum/genetics , Quantitative Trait Loci , Rhizosphere , Soil/chemistry
2.
Br J Cancer ; 83(8): 998-1002, 2000 Oct.
Article in English | MEDLINE | ID: mdl-10993645

ABSTRACT

DT-diaphorase, a cytosolic reductase, has been implicated as an activator of chemotherapeutic prodrugs and a detoxifier of certain potentially carcinogenic xenobiotics. A common C to T nucleotide 609 substitution in DT-diaphorase cDNA has been associated with protein instability and reduced catalytic activity. The degree to which the allelic status of the substitution correlates with enzymatic activity was assessed in 45 normal human skin fibroblast strains using a PCR-RFLP assay. Included in this study was the 3437T strain, which is unique in that it is heterozygous for the polymorphism yet contains undetectable enzymatic activity. An allele-specific RT-PCR-RFLP technique attributed this phenomenon to exclusive DT-diaphorase mRNA expression from the variant allele. Overlap in activities was observed between individual strains homozygous for the wild-type allele and heterozygotes, but the former group displayed enzymatic activity that was on average 2-fold higher. Western blot analysis of the two strains in this panel that are homozygous for the variant allele revealed that they express relatively low amounts of DT-diaphorase protein, consistent with the role of the substitution in protein instability. This work confirms that genotypic status is a reliable initial estimate of DT-diaphorase activity.


Subject(s)
NAD(P)H Dehydrogenase (Quinone)/genetics , NAD(P)H Dehydrogenase (Quinone)/metabolism , Point Mutation , Polymorphism, Restriction Fragment Length , Adolescent , Adult , Cell Line , Cells, Cultured , Child , Child, Preschool , Female , Fibroblasts/enzymology , Genotype , Humans , Infant , Infant, Newborn , Male , Polymerase Chain Reaction/methods , Polymorphism, Genetic , Skin/enzymology
3.
Arch Microbiol ; 172(1): 59-62, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10398753

ABSTRACT

Colonies of Pseudomonas aeruginosa exhibit sectors that were shown to be located at specific intervals within the colony. Maxima in the distribution of sectors were observed every 5 mm as measured from the center of the colony. These maxima correlated with changes in the expansion rates of colonies. The absolute average number of sectors per colony was higher for colonies grown at higher temperatures. These results increase our understanding of colony pattern formation.


Subject(s)
Pseudomonas aeruginosa/growth & development , Colony Count, Microbial
4.
J Bacteriol ; 181(10): 3220-5, 1999 May.
Article in English | MEDLINE | ID: mdl-10322025

ABSTRACT

The expression of nonagglutinating fimbriae (NAF) and mannose-resistant/Proteus-like (MR/P) pili in swarming colonies of Proteus mirabilis was investigated. Elongated swarmer cells do not express pili, and the relative number of bacteria expressing NAF during swarming and early consolidation phases was very low (<5%). Relative expression of NAF in a terrace increased to approximately 30% at 48 h. We also determined the expression of NAF and MR/P pili in two phenotypically distinguishable regions of each terrace. The expression of both NAF and MR/P pili was always higher in the region closer (proximal) to the middle of the colony than in the distal region of the terrace. The relative numbers of bacteria expressing NAF or MR/P pili in the proximal region were between 39.1 and 63% and between 5.9 and 7.7%, respectively. In the distal region, expression levels were between 20.8 and 27.3% and between 3.7 and 5. 6%, respectively. A time course experiment testing NAF expression in both the proximal and distal regions of a terrace indicated that NAF expression in the proximal regions was always higher than in the distal regions and increased to a plateau 40 to 50 h after the start of the swarming phase for any given terrace. These results indicate that expression of NAF or MR/P pili in swarming colonies of P. mirabilis is highly organized, spatially and temporally. The significance of this controlled differentiation remains to be uncovered.


Subject(s)
Agglutination , Fimbriae, Bacterial/metabolism , Gene Expression Regulation, Bacterial , Mannose , Proteus mirabilis/growth & development , Antibodies, Bacterial , Bacterial Adhesion , Cell Division , Colony Count, Microbial , Fimbriae, Bacterial/immunology , Fimbriae, Bacterial/physiology , Fimbriae, Bacterial/ultrastructure , Flagella/metabolism , Flagella/ultrastructure , Fluorescent Antibody Technique , Microscopy, Electron , Phenotype , Proteus mirabilis/genetics , Proteus mirabilis/metabolism , Proteus mirabilis/ultrastructure , Time Factors
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