Identification and characterization of two forms of mouse MUTYH proteins encoded by alternatively spliced transcripts

被引:36
作者
Ichinoe, A
Behmanesh, M
Tominaga, Y
Ushijima, Y
Hirano, S
Sakai, Y
Tsuchimoto, D
Sakumi, K
Wake, N
Nakabeppu, Y [1 ]
机构
[1] Kyushu Univ, Med Inst Bioregulat, Dept Immunobiol & Neurosci, Div Neurofunct Genom, Fukuoka 8128582, Japan
[2] Japan Sci & Technol Agcy JST, Core Res Evolut Sci & Technol CREST, Fukuoka 8128582, Japan
[3] Kyushu Univ, Med Inst Bioregulat, Dept Mol Genet, Div Mol & Cell Therapeut, Oita 8740838, Japan
关键词
D O I
10.1093/nar/gkh214
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are three types of mouse Mutyh mRNAs (type a, b and c) generated by alternative splicing, and type b mRNA is a major form among the three in most of the tissues examined. The level of type c mRNA is relatively high in brain. Type a and b mRNAs were expected to encode 57.7 kDa protein (MUTYHalpha), while type c mRNA had a partly different open reading frame encoding a 50.2 kDa protein (MUTYHbeta). An in vitro translation of type b and c mRNAs produced a 50 kDa MUTYHalpha and 47 kDa MUTYHbeta, respectively. MUTYHalpha and MUTYHbeta were detected in wild-type embryonic stem (ES) cells or thymocytes prepared from wild-type mice, but neither MUTYH-null ES cells nor thymocytes prepared from MUTYH-null mice. Both MUTYHalpha and MUTYHbeta were mainly localized in the nuclei and some in mitochondria in wild-type ES cells. Recombinant MUTYHalpha and beta were expressed as fusion proteins with thioredoxin in Escherichia coli, but only MUTYHalpha was partly soluble and thus could be purified. Recombinant MUTYHalpha possessed DNA glycosylase activities to excise adenine opposite 8-oxoguanine and guanine but not AP lyase activity.
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页码:477 / 487
页数:11
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