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Jain, R.

Publications and source records attributed to Jain, R..

94 records · Page 6Linked to original sources

A matrix protein acts as a cue to preserve collective motility of B. subtilis biofilm cells

Bacteria in nature are usually found in complex multicellular communities, termed biofilms. Biofilms are generally seen as sessile structures, resulting from downregulation of motility. However, during interspecies competition and predation, biofilm cells were shown to migrate towards competitor colonies. Here, we show that a specific extracellular matrix (ECM) protein, TasA, is essential for collective migration toward potential competitors and serves as a developmental cue that increases the formation of motile offspring from sessile chains. We reveal an effective strategy to maintain migration capacities in bacterial biofilms: besides providing a three-dimensional adhesive scaffold for the cells, TasA acts as a signal within the bacterial community.

microbiology↗

Time-restricted foraging under natural light/dark condition shifts the molecular clock in the honey bee, Apis mellifera

Honey bees have a remarkable sense of time and individual honey bee foragers are capable to adjust their foraging activity with respect to the time of food availability. Although, there is plenty of experimental evidence that foraging behavior is guided by the circadian clock, nothing is known about the underlying cellular and molecular mechanisms. Here we present a first study exploring whether the time-restricted foraging under natural light-dark condition affects the molecular clock in honey bees. In an enclosed flight chamber (12m x 4m x 4m), food was presented either for 2 hours in the morning or 2 hours in the afternoon for several consecutive days and daily cycling of the two major clock genes, cryptochrome2 (cry2) and period (per), were analyzed in three different tissues involved in feeding-related behaviors: brain, antennae and subesophageal ganglion (SEG). We found that morning and afternoon trained foragers showed significant phase-differences in the cycling of both clock genes in all three tissues. Furthermore, the phase-differences were more pronounced when the feeder was scented with the general plant odor linalool. Our results clearly demonstrate that foraging time functions as a strong circadian Zeitgeber in honey bees. More surprisingly our results suggest that foraging time might have the potential to override the entrainment effect of the light-dark cycle.

neuroscience↗

Perturbed Mitochondrial Metabolism in Islets from Donors with Type-2 Diabetes

There is a preponderance for genes involved in {beta}-cell function among gene variants associated with future risk of type-2 diabetes (T2D). {beta}-cell function is controlled by metabolism of glucose, yielding signals triggering and amplifying insulin secretion. Perturbed {beta}-cell metabolism is a likely, albeit not proven, cause of T2D. We profiled metabolites in islets from T2D and non-diabetic donors, and found altered levels of mitochondrial metabolites in T2D. Analysis of genes encoding proteins localized to mitochondria (MitoCarta) by RNA-seq in an extended sample of islets revealed genes whose expression was associated with glycaemia- and/or BMI. Expression of two of these, -methylacyl-CoA racemase (AMACR) and methylmalonyl-CoA mutase (MUT), was influenced by genetic variation (cis-eQTL). Silencing of AMACR and MUT in insulin-secreting cells reduced hormone secretion by 40-50%. In conclusion, by linking the metabolome to the transcriptome, we showed that perturbed mitochondrial metabolism is a feature of {beta}-cell dysfunction in T2D.\n\n[Supplementary material is available for this article.]

cell biology↗

The Sequence of 1504 Mutants in the Model Rice Variety Kitaake Facilitates Rapid Functional Genomic Studies

The availability of a whole-genome sequenced mutant population and the cataloging of mutations of each line at a single-nucleotide resolution facilitates functional genomic analysis. To this end, we generated and sequenced a fast-neutron-induced mutant population in the model rice cultivar Kitaake (Oryza sativa L. ssp. japonica), which completes its life cycle in 9 weeks. We sequenced 1,504 mutant lines at 45-fold coverage and identified 91,513 mutations affecting 32,307 genes, 58% of all rice genes. We detected an average of 61 mutations per line. Mutation types include single base substitutions, deletions, insertions, inversions, translocations, and tandem duplications. We observed a high proportion of loss-of-function mutations. Using this mutant population, we identified an inversion affecting a single gene as the causative mutation for the short-grain phenotype in one mutant line with a small segregating population. This result reveals the usefulness of the resource for efficient identification of genes conferring specific phenotypes. To facilitate public access to this genetic resource, we established an open access database called KitBase that provides access to sequence data and seed stocks, enabling rapid functional genomic studies of rice.\n\nOne-sentence summaryWe have sequenced 1,504 mutant lines generated in the short life cycle rice variety Kitaake (9 weeks) and established a publicly available database, enabling rapid functional genomic studies of rice.

plant biology↗