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Jordan T Feigerle

Researcher at Vanderbilt University

Publications -  5
Citations -  420

Jordan T Feigerle is an academic researcher from Vanderbilt University. The author has contributed to research in topics: TAF1 & Histone code. The author has an hindex of 3, co-authored 4 publications receiving 355 citations.

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Analysis of protein dynamics at active, stalled, and collapsed replication forks

TL;DR: A technology called iPOND (isolation of proteins on nascent DNA) is described to analyze proteins at active and damaged replication forks at high resolution and is established as a useful methodology to study DNA replication and chromatin maturation.
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The C Terminus of the RNA Polymerase II Transcription Factor IID (TFIID) Subunit Taf2 Mediates Stable Association of Subunit Taf14 into the Yeast TFIID Complex.

TL;DR: The mechanism through which TAF14 suppresses taf2ts alleles is characterized, shedding light on how Taf2-Taf14 interaction contributes to TFIID complex organization and identifying a potential role for Taf14 in mediating T FIID-chromatin interactions.
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Intrinsic cooperativity potentiates parallel cis-regulatory evolution

TL;DR: It is shown that Mcm1 and Rap1 have the inherent ability to cooperatively activate transcription through contacts with the general transcription factor TFIID, which can account for a pattern of parallel evolution involving the fixation of hundreds of substitutions at a genomic scale.
Journal ArticleDOI

Taf2 mediates DNA binding of Taf14

TL;DR: In this paper , the authors determined the molecular and structural basis by which the YEATS and ET domains of Taf14 bind to the C-terminal tail of the Taf2 and identified a unique DNA-binding activity of the linker region connecting the two domains.
Posted ContentDOI

Intrinsic cooperativity potentiates parallel cis-regulatory evolution

TL;DR: It is shown that Mcm1 and Rap1 have the inherent ability to cooperatively activate transcription through contacts with the general transcription factor TFIID, which can account for a pattern of parallel evolution involving the fixation of hundreds of substitutions at a genomic scale.