Literature DB >> 21795284

Notch-mediated repression of bantam miRNA contributes to boundary formation in the Drosophila wing.

Isabelle Becam1, Neus Rafel, Xin Hong, Stephen M Cohen, Marco Milán.   

Abstract

Subdivision of proliferating tissues into adjacent compartments that do not mix plays a key role in animal development. The Actin cytoskeleton has recently been shown to mediate cell sorting at compartment boundaries, and reduced cell proliferation in boundary cells has been proposed as a way of stabilizing compartment boundaries. Cell interactions mediated by the receptor Notch have been implicated in the specification of compartment boundaries in vertebrates and in Drosophila, but the molecular effectors remain largely unidentified. Here, we present evidence that Notch mediates boundary formation in the Drosophila wing in part through repression of bantam miRNA. bantam induces cell proliferation and we have identified the Actin regulator Enabled as a new target of bantam. Increased levels of Enabled and reduced proliferation rates contribute to the maintenance of the dorsal-ventral affinity boundary. The activity of Notch also defines, through the homeobox-containing gene cut, a distinct population of boundary cells at the dorsal-ventral (DV) interface that helps to segregate boundary from non-boundary cells and contributes to the maintenance of the DV affinity boundary.

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Year:  2011        PMID: 21795284     DOI: 10.1242/dev.064774

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  33 in total

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5.  MiR-206 suppresses proliferation and epithelial-mesenchymal transition of renal cell carcinoma by inhibiting CDK6 expression.

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6.  Notch Represses Transcription by PRC2 Recruitment to the Ternary Complex.

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7.  Bantam regulates the axonal geometry of Drosophila larval brain by modulating actin regulator enabled.

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8.  bantam miRNA is important for Drosophila blood cell homeostasis and a regulator of proliferation in the hematopoietic progenitor niche.

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Review 9.  MicroRNAs as therapeutic targets in chemoresistance.

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Review 10.  MicroRNA function in Drosophila melanogaster.

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