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K. VijayRaghavan

Publications and source records attributed to K. VijayRaghavan.

2 recordsLinked to original sources

Identification and Functional Characterization of Muscle Satellite Cells in Drosophila

Work on genetic model systems such as Drosophila and mouse has shown that the fundamental mechanisms of myogenesis are remarkably similar in vertebrates and invertebrates. Strikingly, however, satellite cells, the adult muscle stem cells that are essential for the regeneration of damaged muscles in vertebrates, have not been reported in invertebrates. In this study we show role of Muscle stem cells (Gunage et al., 2014) identified in a previous study, in muscle regeneration. We show that muscle stem cells lineal descendants are present in adult muscle as small, unfused cells located superficially and in close proximity to the mature muscle fibers. Normally quiescent cells, following muscle fiber injury become mitotically active, engage in Notch-Delta signaling-dependent proliferative activity and generate lineal descendant populations, which fuse with the injured muscle fiber. In view of their strikingly similar morphological and functional features, we consider these novel cells to be Drosophila muscle satellite cells

Developmental Biology

A genome-wide resource for the analysis of protein localisation in Drosophila

The Drosophila genome contains >13,000 protein coding genes, the majority of which remain poorly investigated. Important reasons include the lack of antibodies or reporter constructs to visualise these proteins. Here we present a genome-wide fosmid library of {approx}10,000 GFP-tagged clones, comprising tagged genes and most of their regulatory information. For 880 tagged proteins we have created transgenic lines and for a total of 207 lines we have assessed protein expression and localisation in ovaries, embryos, pupae or adults by stainings and live imaging approaches. Importantly, we can visualise many proteins at endogenous expression levels and find a large fraction of them localising to subcellular compartments. Using complementation tests we demonstrate that two-thirds of the tagged proteins are fully functional. Moreover, our clones also enable interaction proteomics from developing pupae and adult flies. Taken together, this resource will enable systematic analysis of protein expression and localisation in various cellular and developmental contexts.

Genomics