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Jessica A. Talamas

Researcher at University of Pennsylvania

Publications -  8
Citations -  1201

Jessica A. Talamas is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Nuclear pore & Nucleoporin. The author has an hindex of 7, co-authored 8 publications receiving 1094 citations. Previous affiliations of Jessica A. Talamas include Salk Institute for Biological Studies.

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The Genome of M. Acetivorans Reveals Extensive Metabolic and Physiological Diversity

James E. Galagan, +76 more
- 01 Apr 2002 - 
TL;DR: The complete genome sequence of an acetate-utilizing methanogen, Methanosarcina acetivorans C2A, is reported, which indicates the likelihood of undiscovered natural energy sources for methanogenesis, whereas the presence of single-subunit carbon monoxide dehydrogenases raises the possibility of nonmethanogenic growth.
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Cell Cycle-Dependent Differences in Nuclear Pore Complex Assembly in Metazoa

TL;DR: It is shown via RNAi-mediated knockdown that ELYS, a nucleoporin critical for the recruitment of the essential Nup107/160 complex to chromatin, is required for NPC assembly at the end of mitosis but not during interphase, and that the transmembrane nucleiporin POM121 is criticalfor the incorporation of the Nup 107/160complex into new assembly sites specifically during inter phase.
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POM121 and Sun1 play a role in early steps of interphase NPC assembly

TL;DR: POM121 and Sun1, but not the Nup107–160 complex, are required for fusion of the inner and outer nuclear membrane during nuclear pore assembly in interphase of the cell cycle.
Journal ArticleDOI

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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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.