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Experimental Cell Research
Article . 2009 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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Evidence for a direct involvement of hMSH5 in promoting ionizing radiation induced apoptosis

Authors: Tompkins, Joshua D; Wu, Xiling; Chu, Yen-Lin; Her, Chengtao;

Evidence for a direct involvement of hMSH5 in promoting ionizing radiation induced apoptosis

Abstract

Although increasing evidence has suggested that the hMSH5 protein plays an important role in meiotic and mitotic DNA recombinational repair, its precise functions in recombination and DNA damage response are presently elusive. Here we show that the interaction between hMSH5 and c-Abl confers ionizing radiation (IR)-induced apoptotic response by promoting c-Abl activation and p73 accumulation, and these effects are greatly enhanced in cells expressing hMSH5(P29S) (i.e. the hMSH5 variant possessing a proline to serine change within the N-terminal (Px)(5) dipeptide repeat). Our current study provides the first evidence that the (Px)(5) dipeptide repeat plays an important role in modulating the interaction between hMSH5 and c-Abl and alteration of this dipeptide repeat in hMSH5(P29S) leads to increased IR sensitivity owing to enhanced caspase-3-mediated apoptosis. In addition, RNAi-mediated hMSH5 silencing leads to the reduction of apoptosis in IR-treated cells. In short, this study implicates a role for hMSH5 in DNA damage response involving c-Abl and p73, and suggests that mutations impairing this process could significantly affect normal cellular responses to anti-cancer treatments.

Country
United States
Related Organizations
Keywords

570, Ionizing, DNA-Binding Proteins - metabolism, Amino Acid Motifs, DNA Damage - radiation effects, Apoptosis, Cell Cycle Proteins, Transfection, Proto-Oncogene Proteins c-abl - metabolism, Cell Line, Cell Line, Tumor, Radiation, Ionizing, Humans, Phosphorylation - physiology, Genetic - radiation effects, Phosphorylation, Apoptosis - physiology, Proto-Oncogene Proteins c-abl, Recombination, Genetic, Tumor, Radiation, Tumor Suppressor Proteins, Nuclear Proteins, Amino Acid Motifs - physiology, Tumor Protein p73, Recombination, DNA-Binding Proteins, Tumor Suppressor Proteins - metabolism, Apoptosis - radiation effects, Cell Cycle Proteins - metabolism, Nuclear Proteins - metabolism, DNA Damage, HeLa Cells

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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    22
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Average
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
22
Average
Top 10%
Top 10%
bronze