23 research outputs found

    A Novel Zinc Finger Protein Zfp277 Mediates Transcriptional Repression of the Ink4a/Arf Locus through Polycomb Repressive Complex 1

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    Polycomb group (PcG) proteins play a crucial role in cellular senescence as key transcriptional regulators of the Ink4a/Arf tumor suppressor gene locus. However, how PcG complexes target and contribute to stable gene silencing of the Ink4a/Arf locus remains little understood.We examined the function of Zinc finger domain-containing protein 277 (Zfp277), a novel zinc finger protein that interacts with the PcG protein Bmi1. Zfp277 binds to the Ink4a/Arf locus in a Bmi1-independent manner and interacts with polycomb repressor complex (PRC) 1 through direct interaction with Bmi1. Loss of Zfp277 in mouse embryonic fibroblasts (MEFs) caused dissociation of PcG proteins from the Ink4a/Arf locus, resulting in premature senescence associated with derepressed p16(Ink4a) and p19(Arf) expression. Levels of both Zfp277 and PcG proteins inversely correlated with those of reactive oxygen species (ROS) in senescing MEFs, but the treatment of Zfp277(-/-) MEFs with an antioxidant restored the binding of PRC2 but not PRC1 to the Ink4a/Arf locus. Notably, forced expression of Bmi1 in Zfp277(-/-) MEFs did not restore the binding of Bmi1 to the Ink4a/Arf locus and failed to bypass cellular senescence. A Zfp277 mutant that could not bind Bmi1 did not rescue Zfp277(-/-) MEFs from premature senescence.Our findings implicate Zfp277 in the transcriptional regulation of the Ink4a/Arf locus and suggest that the interaction of Zfp277 with Bmi1 is essential for the recruitment of PRC1 to the Ink4a/Arf locus. Our findings also highlight dynamic regulation of both Zfp277 and PcG proteins by the oxidative stress pathways

    A trend analysis on the quality and quantity of Japanese research papers in an international perspective

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    三題噺:SGML・コンテンツ・大学ランキング

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    The latest information related technology. SGML and full-text database.

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    Address for correspondence:

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    The paper describes the construction and functions of the Citation Database for Japanese Papers (CJP) developed at the National Institute of Informatics, Japan (NII), and the Impact Factors of CJP’s source journals. Then statistical analyses of multidimensional scaling on citation counts for the academic society journals to measure relationship among the societies are described. We also introduce a new citation navigation system, CiNii, which enables users to access various resources provided by NII, such as NACSIS Electronic Library Service (NACSIS-ELS) to get electronic full-text of journal articles through citation links. Recent political developments in Japan towards enhancement of scientific information infrastructure are also introduced with its implication to research evaluation systems incorporating citation analyses

    日本國家資訊基礎建設(NII)之新發展

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