Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication

Bibliographic Details
Main Author: Bhattacharjee, Anukana, M.S.
Language:English
Published: University of Cincinnati / OhioLINK 2017
Subjects:
Online Access:http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504781845245038
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spelling ndltd-OhioLink-oai-etd.ohiolink.edu-ucin15047818452450382021-08-03T07:04:08Z Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication Bhattacharjee, Anukana, M.S. Biogeochemistry Telomere Replication CTC1 STN1 TEN1 DNA binding OB fold Telomeres are the protective DNA-protein complexes at the ends of chromosomes. Mammalian telomeres are composed of double-stranded DNA with a repetitive sequence (TTAGGG) followed by a short single-stranded overhang. The DNA is bound by a series of proteins that prevent chromosome fusions and protect the DNA terminus from being sensed as damage. These telomere proteins also aid in telomere replication. Shelterin, the primary telomere protein complex, binds to both the double- and single-strand regions of the telomere. Shelterin is important for protecting telomeres from being sensed as damage. It also brings in telomerase for telomere extension. The other major telomere protein complex is CST (CTC1-STN1-TEN1). CST functions in telomere replication first by aiding passage of the replication machinery through the telomere duplex and then enabling fill-in synthesis of the telomeric C-strand following telomerase action. CST also has genome-wide roles in the resolution of replication stress. CST resembles Replication Protein A (RPA) in that it binds ssDNA and STN1 and TEN1 are structurally similar to RPA2 and RPA3. Here we address CST mechanism by using STN1 OB-fold mutant (STN1-OBM) to examine the relationship between DNA binding and CST function. In vivo, STN1-OBM affects resolution of endogenous replication stress and telomere duplex replication but telomeric C-strand fill-in and new origin firing after exogenous replication stress are unaffected. In vitro binding studies show that STN1 directly engages both short and long ssDNA, however STN1-OBM preferentially destabilizes binding to short substrates. CST is expected to engage DNA substrates of varied length and structure as it acts to resolve different replication problems. Since STN1-OBM will alter CST binding to only some of these substrates, the mutant should affect resolution of only a subset of replication problems, as was observed in the STN1-OBM cells. The in vitro studies also provide insight into CST binding mechanism. Like RPA, CST likely contacts DNA via multiple OB folds. However, the importance of STN1 for binding short substrates indicates differences in the architecture of CST and RPA DNA-protein complexes. Although the architecture of DNA binding differ for RPA and CST, their overall structural similarity motivated us to use RPA as a model to investigate DNA binding properties underlying CST function. RPA binds to ssDNA with high affinity, yet individual OB-folds can micro-dissociate from the DNA promoting sliding of RPA on the DNA, melting of dsDNA or secondary structures, recruitment of interaction partners. By using single molecule fluorescence assays, we show that CST cannot melt dsDNA but it can resolve secondary structures such as G4. The efficiency of G4 unfolding by CST, and its known abundance in G-rich regions genome-wide could explain its role in resolution of replication stress. Our work has also shown that CST can recognize ss-dsDNA junctions which start to explain the incremental nature of the telomeric C-strand fill-in reaction after G-strand extension by telomerase. Overall, our work provides insight into the mechanism by which CST might resolve replication issues at the telomere and genome wide. 2017-12-05 English text University of Cincinnati / OhioLINK http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504781845245038 http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504781845245038 unrestricted This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
collection NDLTD
language English
sources NDLTD
topic Biogeochemistry
Telomere
Replication
CTC1 STN1 TEN1
DNA binding
OB fold
spellingShingle Biogeochemistry
Telomere
Replication
CTC1 STN1 TEN1
DNA binding
OB fold
Bhattacharjee, Anukana, M.S.
Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication
author Bhattacharjee, Anukana, M.S.
author_facet Bhattacharjee, Anukana, M.S.
author_sort Bhattacharjee, Anukana, M.S.
title Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication
title_short Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication
title_full Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication
title_fullStr Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication
title_full_unstemmed Characterization of the DNA Binding Properties of CST (CTC1-STN1-TEN1) And Their Importance for CST Function in Telomeric as well as Genome-wide Replication
title_sort characterization of the dna binding properties of cst (ctc1-stn1-ten1) and their importance for cst function in telomeric as well as genome-wide replication
publisher University of Cincinnati / OhioLINK
publishDate 2017
url http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504781845245038
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