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Volume 24 Issue 7, July 2014

Research Highlight

  • Mediator is a large and structurally dynamic protein complex that is globally required for eukaryotic transcription by RNA polymerase II. In a recent paper published in Cell Research, Wang et al. report for the first time the location of distinct subunits and redefine domains in the S. cerevisiae Mediator complex.

    • Nicholas C Sennett
    • Dylan J Taatjes
    Research Highlight

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  • Regenerative medicine for cardiovascular disease requires effective approaches for therapeutic revascularization. In a recent paper in Cell Research, Sahara et al. establish a new role for Notch signaling to promote endothelial progenitor differentiation, and develop a protocol based on Notch inhibition in endothelial progenitors to markedly enhance the yield and purity of functional endothelial cells differentiated from embryonic stem cells.

    • Bing Zhang
    • William T Pu
    Research Highlight
  • Piwi-interacting RNAs (piRNAs) have a major function in the repression of transposable elements in the germline; in addition, they have been proposed to regulate gene expression. A recent study in Cell Research reveals a general role for piRNAs in the massive mRNA decay during mouse spermiogenesis, reinforcing this emerging function of piRNAs.

    • Martine Simonelig
    Research Highlight
  • A recent study published in Science reveals the mechanism and biological importance of DNA damage response abrogation in mitotic cells.

    • Rimma Belotserkovskaya
    • Stephen P Jackson
    Research Highlight
  • Macroautophagy has been implicated in numerous diseases, yet our understanding of the proteins responsible for the turnover of specific cargo by autophagy is limited. In a recent paper published in Nature, Mancias et al. used quantitative proteomics to identify a cohort of autophagosome-enriched proteins, one of which, nuclear receptor coactivator 4 (NCOA4) was shown to be required for the selective delivery of ferritin to the lysosome, ultimately regulating intracellular iron by autophagic turnover of ferritin, or ferritinophagy.

    • Megan Goodall
    • Andrew Thorburn
    Research Highlight
  • Akt phosphorylation at S473 and T308 has been believed to be the prerequisites for its activation for years. Now, new phosphorylation event on Akt is identified and can trigger Akt activation and lead to its downstream oncogenic events.

    • Yuan Gao
    • Asad Moten
    • Hui-Kuan Lin
    Research Highlight
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