MLH1-mediated recruitment of FAN1 to chromatin for the induction of apoptosis triggered by O6-methylguanine

Persistent ID (NDL): info:ndljp/pid/11673171

Material type: 博士論文

Author: Rikitake, Mihokoほか

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Publication date: 2020-03-14

Material Format: Digital

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Name of awarding university/degree: 福岡歯科大学,博士（歯学）

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Note (General)：: O6 -Methylguanines (O6 -meG), which are produced in DNA by the action of alkylating agents, are mutagenic and cytotoxic, and induce apoptosis in a mis...

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Material Type: 博士論文
Title: MLH1-mediated recruitment of FAN1 to chromatin for the induction of apoptosis triggered by O6-methylguanine
Author/Editor: Rikitake, Mihoko
Fujikane, Ryosuke
Obayashi, Yuko
Oka, Kyoko
Ozaki, Masao
Hidaka, Masumi
Publication Date: 2020-03-14
Publication Date (W3CDTF): 2020-03-14
Alternative Title: MLH1-mediated recruitment of FAN1 to chromatin for the induction of apoptosis triggered by O6-methylguanine
Degree grantor/type: 福岡歯科大学
Date Granted: 2020-03-14
Date Granted (W3CDTF): 2020-03-14
Dissertation Number: 甲第311号
Degree Type: 博士（歯学）
Conferring No. (Dissertation): 甲第311号
Text Language Code: eng
Subject Heading: apoptosis
FANCD2 and FANCI-associated nuclease 1 (FAN1)
O6-methylguanine
mismatch repair (MMR)
MLH1
Note (General): O6 -Methylguanines (O6 -meG), which are produced in DNA by the action of alkylating agents, are mutagenic and cytotoxic, and induce apoptosis in a mismatch repair (MMR) protein-dependent manner. To understand the molecular mechanism of O6 -meG-induced apoptosis, we performed functional analyses of FANCD2 and FANCI-associated nuclease 1 (FAN1), which was identified as an interacting partner of MLH1. Immunoprecipitation analyses showed that FAN1 interacted with both MLH1 and MSH2 after treatment with N-methyl-N-nitrosourea (MNU), indicating the formation of a FAN1-MMR complex. In comparison with control cells, FAN1-knockdown cells were more resistant to MNU, and the appearances of a sub-G1 population and caspase-9 activation were suppressed. FAN1 formed nuclear foci in an MLH1-dependent manner after MNU treatment, and some were colocalized with both MLH1 foci and single-stranded DNA (ssDNA) created at damaged sites. Under the same condition, FANCD2 also formed nuclear foci, although it was dispensable for the formation of FAN1 foci and ssDNA. MNU-induced formation of ssDNA was dramatically suppressed in FAN1-knockdown cells. We therefore propose that FAN1 is loaded on chromatin through the interaction with MLH1 and produces ssDNA by its exonuclease activity, which contributes to the activation of the DNA damage response followed by the induction of apoptosis triggered by O6 -meG.
Persistent ID (NDL): info:ndljp/pid/11673171
https://dl.ndl.go.jp/pid/11673171
Collection: 障害者向け資料
Collection (Materials For Handicapped People:1): テキストデータ
Collection (particular): 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文
https://dl.ndl.go.jp/collections/A00014
Acquisition Basis: 博士論文（自動収集）
Date Accepted (W3CDTF): 2021-05-20T03:24:30+09:00
Date Created (W3CDTF): 2020-04-07
Format (IMT): application/pdf
Access Restrictions: 国立国会図書館内限定公開
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Availability of remote photoduplication service: 可
Original Material (URI): https://doi.org/10.1111/gtc.12748
Periodical Title (URI): http://id.nii.ac.jp/1167/00000094/
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