Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.818109
Title: Molecular mechanism of KAP1-dependent transcriptional silencing
Author: Stoll, Guido
ISNI:       0000 0004 9359 5444
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2019
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Abstract:
Retroviruses can integrate their DNA into the host-cell genome. Inherited retroviral DNA and other transposable elements account for at least half of the human genome. Transcription of transposable elements is tightly regulated to restrict their proliferation and prevent toxic gene expression. A major factor contributing to the repression of potentially harmful retroelements is KRAB-associated protein 1 (KAP1, also known as TRIM28 or TIF1β). Following its recruitment to retrotransposons by sequence-specific KRAB domain-containing zinc finger proteins (KRAB-ZFPs), KAP1 induces the assembly of an epigenetic silencing complex, with chromatin remodeling activities that repress transcription of the targeted retrotransposon and adjacent genes. To understand the molecular basis of KAP1-dependent transcriptional regulation I determined the crystal structure of the RBCC domain of KAP1. My structural and biophysical data demonstrate that KAP1 forms antiparallel dimers, which further assemble into tetramers and higher-order oligomers in a concentration-dependent manner. Structure-based mutations in the B-box 1 domain prevented higher-order oligomerization and resulted in significant defects in KAP1-dependent transcriptional repression, suggesting that self-assembly may contribute to KAP1 function. Furthermore, I characterized the interaction of KAP1 with the KRAB domain of KRAB-ZFPs, which is crucial for recruitment of KAP1 to its genomic targets. My data show that each KAP1 dimer can only bind a single KRAB domain, resulting in a 2:1 stoichiometry. Moreover, my crystal structure of the KAP1 RBCC dimer identifies the KRAB domain binding site, in the coiled-coil domain near the dyad. Mutations at this site abolished KRAB binding and transcriptional silencing activity of KAP1. This work identifies the interaction interfaces in the KAP1 RBCC domain responsible for self-association and KRAB binding and establishes their role in retrotransposon silencing.
Supervisor: Modis, Yorgo Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.818109  DOI:
Keywords: transcriptional repressor ; epigenetic silencing ; endogenous retrovirus ; transposable element ; ubiquitin E3 ligase
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