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dc.contributor.advisorLiu, Wenshe R
dc.creatorWang, Wei
dc.date.accessioned2019-01-23T21:44:46Z
dc.date.created2018-12
dc.date.issued2018-11-12
dc.date.submittedDecember 2018
dc.identifier.urihttp://hdl.handle.net/1969.1/174597
dc.description.abstractFor eukaryotes, DNA is maintained in the form of chromatin, which is comprised of millions of repeated nucleosomes. Each nucleosome is assembled by wrapping 147 base pairs (bp) of DNA around a histone octamer containing 2 copies of H2A, H2B, H3 and H4. Histone residues undergo a plethora of post-translational modifications (PTM), which have a great impact on the conformation and organization of chromatin and eventually lead to significant epigenetic changes related to genetic events such as transcription, replication and DNA repair. SIRT6 and SIRT7 are the newest members of the Sirtuin deacetylase family. With a unique NAD^+ dependent mechanism, Sirtuin enzymes remove histone lysine acetylation and acylations. SIRT6 has been reported as a site-specific histone deacetylase targeting H3K9 acetylation (H3K9ac) and H3K56 acetylation (H3K56ac). SIRT7 was reported to be specific for H3K18 acetylation (H3K18ac). Compared to other Sirtuin members, SIRT6 and SIRT7 exhibit very weak in vitro deacetylation activities on acetyl-histones and acetyl-peptides, but become much more active on acetylnucleosomes. However, all previous SIRT6 and SIRT7 histone targets were identified using acetyl-peptides as substrates, raising the question whether new active sites could be discovered if acetyl-nucleosomes were used as substrates The main obstacle to biochemical study on nucleosomal level is the synthesis of homogenous nucleosomes with site-specific PTM. In this work, using unnatural amino acid incorporation technique, we synthesized homogenous histone H3 substrates with iii acylation at defined lysine sites, assembled them into acyl- nucleosomes, and screened for targets of SIRT6 and SIRT7 with a novel fluorescence-based deacylation assay. As a result, we discovered H3 K18 and H3 K27 as the new targets for SIRT6, H3 K36 as the new target for SIRT7. The newly identified targets were confirmed in vitro using sitespecific acetyl-nucleosomes, and in vivo using SIRT6 or SIRT7 overexpressed mammalian cell model. Using Chip-Seq assay, H3K36ac was discovered to be downregulated at specific gene promoters, nucleoli and telomeres. SIRT7 deacetylation is activated by extranucleosomal DNA through its electrostatic bridging between histone and enzyme.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.subjectSIRT6en
dc.subjectSIRT7en
dc.subjectclick chemistryen
dc.subjectunnatural amino acid incorporationen
dc.subjectsite-specificityen
dc.subjectnucleosomeen
dc.titleSIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomesen
dc.typeThesisen
thesis.degree.departmentChemistryen
thesis.degree.disciplineChemistryen
thesis.degree.grantorTexas A & M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.levelDoctoralen
dc.contributor.committeeMemberBegley, Tadhg P
dc.contributor.committeeMemberBarondeau, David P
dc.contributor.committeeMemberStraight, Paul D
dc.type.materialtexten
dc.date.updated2019-01-23T21:44:46Z
local.embargo.terms2020-12-01
local.embargo.lift2020-12-01
local.etdauthor.orcid0000-0002-7514-539X


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