NEIL1 mRNA Splicing Variants are Expressed in Normal Mouse Organs
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概要
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Oxidized pyrimidines are mainly repaired by base excision repair, which is initiated by damage-specific DNA glycosylases. NEIL1, the mammalian homolog of Escherichia coli endonuclease VIII and a major DNA glycosylase, initiates repair of oxidized pyrimidines. Here, we investigated the expression of two putative variant mouse NEIL1 (mNEIL1) mRNAs—variant 1 ("Neil1 protein" mRNA; BC043297 in the NCBI database) and variant 2 ("unnamed protein" mRNA; AK040802 in the NCBI database)—in normal mouse organs. Reverse transcription-PCR showed that both mRNAs were expressed in total RNA samples from 9 organs. Immunoblot analysis of a nuclear extract from normal mouse liver revealed three bands corresponding to full-length mNEIL1 protein and the two predicted variant proteins. However, neither variant protein, which included an N-terminal enzymatic activity domain deduced from the mRNA variants, were enzymatically active under multiple reaction conditions when expressed as his-tagged recombinant proteins. Nevertheless, recombinant variant 1 protein influenced mNEIL1 activity, while recombinant variant 2 protein had no influence. These results suggest that mNEIL1 mRNA variants are expressed in a variety of organs in normal mice and that variant 1 protein may regulate mNEIL1 activity.
著者
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Kubo Kihei
Department Of Advanced Pathobiology Graduate School Of Life & Environmental Sciences Osaka Prefe
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Yamamoto Ryohei
Department Of Advanced Pathobiology Graduate School Of Life & Environmental Sciences Osaka Prefe
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Yamamoto Mizuki
Department Of Cancer Biology Division Of Cellular And Molecular Biology University Of Tokyo
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Ide Hiroshi
Department Of Chemistry Faculty Of Science Kyushu University
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Tajima Tomoko
Department Of Veterinary Microbiology College Of Agiculture Osaka Prefecture University
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MATSUYAMA Satoshi
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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KUSAKA Hiroyuki
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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MASATSUGU Hideaki
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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MASATSUGU Hideaki
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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KUBO Kihei
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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YAMAMOTO Mizuki
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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TAJIMA Tomoko
Department of Infectious Diseases Control, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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Yamamoto Ryohei
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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KUSAKA Hiroyuki
Department of Advanced Pathobiology, Graduate School of Life & Environmental Sciences, Osaka Prefecture University
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