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Pau Pascual-Garcia

Researcher at University of Pennsylvania

Publications -  17
Citations -  741

Pau Pascual-Garcia is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Chromatin & Nuclear pore. The author has an hindex of 13, co-authored 17 publications receiving 614 citations. Previous affiliations of Pau Pascual-Garcia include Catalan Institution for Research and Advanced Studies & Utrecht University.

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The mRNA Export Factor Sus1 Is Involved in Spt/Ada/Gcn5 Acetyltransferase-mediated H2B Deubiquitinylation through Its Interaction with Ubp8 and Sgf11

TL;DR: It is demonstrated that Sus1 is involved in the SAGA-dependent histone H2B deubiquitinylation and maintenance of normal H3 methylation levels and the Sus1-Sgf11-Ubp8 module could work at the junction between SAGa-dependent transcription and nuclear mRNA export.
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Metazoan Nuclear Pores Provide a Scaffold for Poised Genes and Mediate Induced Enhancer-Promoter Contacts

TL;DR: The presence of multiple Nups at promoters, enhancers, and insulators in the Drosophila genome is identified and a functional role for Nup98 is uncovered in mediating enhancer-promoter looping at ecdysone-inducible genes.
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Sus1 is recruited to coding regions and functions during transcription elongation in association with SAGA and TREX2

TL;DR: It is shown that Sus1 is required during transcription elongation and is associated with the elongating form of RNA Polymerase II (RNAP II) phosphorylated on Ser5 and Ser2 of the C-terminal domain (CTD), and that Sgf73 is necessary for association of Sus1 with both SAGA and TREX2, and that its absence dramatically reduces Sus1 occupancy of UAS and ORF sequences.
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Nucleoporin Nup98 associates with Trx/MLL and NSL histone-modifying complexes and regulates Hox gene expression.

TL;DR: Roles of Nup98 in epigenetic regulation that may underlie the basis of oncogenicity of N up98 fusions in leukemia are introduced.
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Core Components of the Nuclear Pore Bind Distinct States of Chromatin and Contribute to Polycomb Repression.

TL;DR: This investigation uncovered differential binding of these NPC subunits, where Nup107 preferentially targets active genes while Nup93 associates primarily with Polycomb-silenced regions, and lend to a model where different nuclear pores bind different types of chromatin via interactions with specific NPC sub-complexes, and a subset of Polycomb domains is stabilized by interactions with N up93.