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Angelika Lebersorger

Researcher at Research Institute of Molecular Pathology

Publications -  4
Citations -  1082

Angelika Lebersorger is an academic researcher from Research Institute of Molecular Pathology. The author has contributed to research in topics: Heterochromatin & Regulation of gene expression. The author has an hindex of 4, co-authored 4 publications receiving 1038 citations.

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Functional mammalian homologues of the Drosophila PEV‐modifier Su(var)3‐9 encode centromere‐associated proteins which complex with the heterochromatin component M31

TL;DR: Immodetection of endogenous Suv39h1/SUV39H1 proteins in a variety of mammalian cell lines reveals enriched distribution at heterochromatic foci during interphase and centromere‐specific localization during metaphase, and indicates the existence of a mammalian SU(VAR) complex.
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Mammalian homologues of the Polycomb-group gene Enhancer of zeste mediate gene silencing in Drosophila heterochromatin and at S. cerevisiae telomeres

TL;DR: The isolation of human (EZH2) and mouse (Ezh1) homologues of the Drosophila Polycomb‐group (Pc‐G) gene Enhancer of zeste [E(z)], a crucial regulator of homeotic gene expression implicated in the assembly of repressive protein complexes in chromatin, is described, indicating that silencing mechanism(s) may be broadly conserved in eukaryotes.
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Isolation and Characterization of Suv39h2, a Second Histone H3 Methyltransferase Gene That Displays Testis-Specific Expression

TL;DR: Immunolocalization of Suv39h2 protein during spermatogenesis indicates enriched distribution at the heterochromatin from the leptotene to the round sperMatid stage, suggesting an additional function of the Suv 39h2 HMTase in organizing meiotic heterochromeatin that may even impart an epigenetic imprint to the male germ line.
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The murine polycomb-group genes Ezh1 and Ezh2 map close to Hox gene clusters on mouse Chromosomes 11 and 6

TL;DR: E(z) appears to be a pleiotropic Pc-G gene with functions in chromatin architecture, gene regulation, and growth control, and mammalian E(Z)related genes are likely to participate in developmental switches that may trigger differentiation or proliferation.