Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements

Thesis advisor: Hugh P. Cam === Chromatin is the site of numerous structural features that contribute to the regulation of the genome. Although numerous posttranslational modifications to the histone proteins that make up chromatin have been identified, it remains unclear whether and to what extent...

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Main Author: Grady, Patrick James Robert
Format: Others
Language:English
Published: Boston College 2015
Subjects:
Online Access:http://hdl.handle.net/2345/bc-ir:104931
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spelling ndltd-BOSTON-oai-dlib.bc.edu-bc-ir_1049312019-05-10T07:38:00Z Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements Grady, Patrick James Robert Thesis advisor: Hugh P. Cam Text thesis 2015 Boston College English electronic application/pdf Chromatin is the site of numerous structural features that contribute to the regulation of the genome. Although numerous posttranslational modifications to the histone proteins that make up chromatin have been identified, it remains unclear whether and to what extent these modifications might regulate transposons and other repetitive sequences. One such modification is methylation of histone H3 lysine 4 (H3K4me), which is catalyzed by Set1 and its associated complex Set1C/COMPASS. Although H3K4me is associated with actively transcribed regions in euchromatin, an emerging body of evidence suggests that Set1-mediated transcriptional control is often repressive. This thesis work describes expanded functions for Set1C/COMPASS as a regulatory module with roles throughout the genome. We identify novel locus-dependent repressive functions for Set1 at repetitive genomic regions. Interestingly, Set1 has multiple repressive modes that are dependent and independent of H3K4me. Additionally, we show that Set1 controls the nuclear organization of Tf2 retrotransposons by antagonizing H3K4 acetylation. We describe how the roles of Set1 in the nuclear organization and transcriptional repression of Tf2 cooperate to restrict Tf2 transposition. Finally, we identify an H3K4-dependent role in countering the reduced dosage of histone H3 genes to help maintain genome stability and silencing of Tf2s and pericentromeric heterochromatin. Our study considerably expands the regulatory repertoire of an important histone modifier and highlights the multifaceted function by a highly conserved chromatin-modifying complex with diverse roles in genome control. Chromatin Epigenetics Genetics Genomics Copyright is held by the author. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0). Thesis (PhD) — Boston College, 2015. Submitted to: Boston College. Graduate School of Arts and Sciences. Discipline: Biology. http://hdl.handle.net/2345/bc-ir:104931
collection NDLTD
language English
format Others
sources NDLTD
topic Chromatin
Epigenetics
Genetics
Genomics
spellingShingle Chromatin
Epigenetics
Genetics
Genomics
Grady, Patrick James Robert
Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements
description Thesis advisor: Hugh P. Cam === Chromatin is the site of numerous structural features that contribute to the regulation of the genome. Although numerous posttranslational modifications to the histone proteins that make up chromatin have been identified, it remains unclear whether and to what extent these modifications might regulate transposons and other repetitive sequences. One such modification is methylation of histone H3 lysine 4 (H3K4me), which is catalyzed by Set1 and its associated complex Set1C/COMPASS. Although H3K4me is associated with actively transcribed regions in euchromatin, an emerging body of evidence suggests that Set1-mediated transcriptional control is often repressive. This thesis work describes expanded functions for Set1C/COMPASS as a regulatory module with roles throughout the genome. We identify novel locus-dependent repressive functions for Set1 at repetitive genomic regions. Interestingly, Set1 has multiple repressive modes that are dependent and independent of H3K4me. Additionally, we show that Set1 controls the nuclear organization of Tf2 retrotransposons by antagonizing H3K4 acetylation. We describe how the roles of Set1 in the nuclear organization and transcriptional repression of Tf2 cooperate to restrict Tf2 transposition. Finally, we identify an H3K4-dependent role in countering the reduced dosage of histone H3 genes to help maintain genome stability and silencing of Tf2s and pericentromeric heterochromatin. Our study considerably expands the regulatory repertoire of an important histone modifier and highlights the multifaceted function by a highly conserved chromatin-modifying complex with diverse roles in genome control. === Thesis (PhD) — Boston College, 2015. === Submitted to: Boston College. Graduate School of Arts and Sciences. === Discipline: Biology.
author Grady, Patrick James Robert
author_facet Grady, Patrick James Robert
author_sort Grady, Patrick James Robert
title Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements
title_short Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements
title_full Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements
title_fullStr Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements
title_full_unstemmed Epigenome control by chromatin modifiers: roles for histone H3 lysine modifiers in the regulation of repetitive elements
title_sort epigenome control by chromatin modifiers: roles for histone h3 lysine modifiers in the regulation of repetitive elements
publisher Boston College
publishDate 2015
url http://hdl.handle.net/2345/bc-ir:104931
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