Sortase-mediated ubiquitylation of Histone H2B and its biological consequences

Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Biology, February 2013.

Bibliographic Details
Main Author: Díaz-Torres, José J. (José Javier)
Other Authors: Hidde L. Ploegh.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2013
Subjects:
Online Access:http://hdl.handle.net/1721.1/79180
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author Díaz-Torres, José J. (José Javier)
author2 Hidde L. Ploegh.
author_facet Hidde L. Ploegh.
Díaz-Torres, José J. (José Javier)
author_sort Díaz-Torres, José J. (José Javier)
collection MIT
description Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Biology, February 2013.
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spelling mit-1721.1/791802019-04-11T11:05:01Z Sortase-mediated ubiquitylation of Histone H2B and its biological consequences Díaz-Torres, José J. (José Javier) Hidde L. Ploegh. Massachusetts Institute of Technology. Department of Biology. Massachusetts Institute of Technology. Department of Biology. Biology. Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Biology, February 2013. Cataloged from PDF version of thesis. "February 2013." Includes bibliographical references (p. 20-22). Regulation of gene expression has been a longstanding puzzle in the understanding of cell biological processes. Histone 2B (H2B) ubiquitylation has been suggested to collaborate in the complex mechanisms that control the activation or silencing of genes. Here we try to explain how we could use the sortagging technique to control ubiquitylation events inside the nuclear envelope. We were able to perform in Saccharomyces cerevisiae an in vivo SrtA-mediated intramolecular circularization reaction of the NLS-tagged enhanced green fluorescent protein that contains an Nterminal glycine residue and a C-terminal sortagging motif (G-NLS-eGFP-LPETGmyc). However, nuclear fractionation experiments were unable to show efficient nuclear localization of NLS-SrtA and the modified eGFP. We designed and expressed in yeast a sortaggable H2B molecule that could be used for intranuclear sortase-mediated histone ubiquitylation. For the benefit of future SrtA experiments, we produced mouse polyclonal antibodies against Staphylococcus aureus and Streptomyces pyogenes SrtA. These experiments will help to further the development of intranuclear sortagging reactions in yeast and to apply the technique to perform inducible H2B ubiquitylation. by José J. Díaz-Torres. S.M. 2013-06-17T19:45:32Z 2013-06-17T19:45:32Z 2012 2013 Thesis http://hdl.handle.net/1721.1/79180 844346110 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 28 p. application/pdf Massachusetts Institute of Technology
spellingShingle Biology.
Díaz-Torres, José J. (José Javier)
Sortase-mediated ubiquitylation of Histone H2B and its biological consequences
title Sortase-mediated ubiquitylation of Histone H2B and its biological consequences
title_full Sortase-mediated ubiquitylation of Histone H2B and its biological consequences
title_fullStr Sortase-mediated ubiquitylation of Histone H2B and its biological consequences
title_full_unstemmed Sortase-mediated ubiquitylation of Histone H2B and its biological consequences
title_short Sortase-mediated ubiquitylation of Histone H2B and its biological consequences
title_sort sortase mediated ubiquitylation of histone h2b and its biological consequences
topic Biology.
url http://hdl.handle.net/1721.1/79180
work_keys_str_mv AT diaztorresjosejjosejavier sortasemediatedubiquitylationofhistoneh2banditsbiologicalconsequences