T
Thomas E. Wilson
Researcher at University of Michigan
Publications - 104
Citations - 5028
Thomas E. Wilson is an academic researcher from University of Michigan. The author has contributed to research in topics: Non-homologous end joining & DNA repair. The author has an hindex of 39, co-authored 101 publications receiving 4564 citations. Previous affiliations of Thomas E. Wilson include University of Sheffield.
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Journal ArticleDOI
Nonhomologous end joining in yeast.
TL;DR: How double-strand break structure, the yeast NHEJ proteins, and alternative rejoining mechanisms influence the accuracy of break repair is reviewed and how the balance between N HEJ and homologous repair is regulated by cell state to promote genome preservation is considered.
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Repair of double-strand breaks by end joining.
TL;DR: There is great interest in defining alt-N HEJ more precisely, including its regulation relative to c-NHEJ, in light of evidence that alt- NHEJ can execute chromosome rearrangements.
Journal ArticleDOI
Rate of elongation by RNA polymerase II is associated with specific gene features and epigenetic modifications
Artur Veloso,Killeen S. Kirkconnell,Brian Magnuson,Benjamin Biewen,Michelle T. Paulsen,Thomas E. Wilson,Mats Ljungman +6 more
TL;DR: It is found that genes with rapid elongation rates showed higher densities of H3K79me2 and H4K20me1 histone marks compared to slower elongating genes, and features that negatively correlated with elongation rate included the density of exons, long terminal repeats, GC content of the gene, and DNA methylation density in the bodies of genes.
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Mycobacterial Ku and Ligase Proteins Constitute a Two-Component NHEJ Repair Machine
Marina Della,Phillip L. Palmbos,Hui Min Tseng,Louise M. Tonkin,Louise M. Tonkin,James M. Daley,Leana M Topper,Robert S. Pitcher,Alan E. Tomkinson,Thomas E. Wilson,Aidan J. Doherty +10 more
TL;DR: It is demonstrated that prokaryotic Ku and ligase form a bona fide NHEJ system that encodes all the recognition, processing, and ligation activities required for DSB repair.
Journal ArticleDOI
Yeast Tdp1 and Rad1-Rad10 function as redundant pathways for repairing Top1 replicative damage
John R. Vance,Thomas E. Wilson +1 more
TL;DR: It is reported that the tyrosyl-DNA phosphodiesterase Tdp1 and the structure-specific endonuclease Rad1-Rad10 function as primary alternative pathways of Top1 repair in Saccharomyces cerevisiae and it is shown that yeast lacking the Rad1/Rad10-related proteins Mus81-Mms4 display a unique pattern of camptothecin sensitivity and suggest a concerted model for the action of these endonucleases.