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.
引用
收藏
页码:477 / 487
页数:11
相关论文
共 25 条
[1]   Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors [J].
Al-Tassan, N ;
Chmiel, NH ;
Maynard, J ;
Fleming, N ;
Livingston, AL ;
Williams, GT ;
Hodges, AK ;
Davies, DR ;
David, SS ;
Sampson, JR ;
Cheadle, JR .
NATURE GENETICS, 2002, 30 (02) :227-232
[2]   OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[3]   Base excision repair of 8-hydroxyguanine protects DNA from endogenous oxidative stress [J].
Boiteux, S ;
Radicella, JP .
BIOCHIMIE, 1999, 81 (1-2) :59-67
[4]   Rat MYH, a glycosylase for repair of oxidatively damaged DNA, has brain-specific isoforms that localize to neuronal mitochondria [J].
Englander, EW ;
Hu, ZY ;
Sharma, A ;
Lee, HM ;
Wu, ZH ;
Greeley, GH .
JOURNAL OF NEUROCHEMISTRY, 2002, 83 (06) :1471-1480
[5]   MutY catalytic core, mutant and bound adenine structures define specificity for DNA repair enzyme superfamily [J].
Guan, Y ;
Manuel, RC ;
Arvai, AS ;
Parikh, SS ;
Mol, CD ;
Miller, JH ;
Lloyd, S ;
Tainer, JA .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (12) :1058-1064
[6]   Mutator phenotype of MUTYH-null mouse embryonic stem cells [J].
Hirano, S ;
Tominaga, Y ;
Ichinoe, A ;
Ushijima, Y ;
Tsuchimoto, D ;
Honda-Ohnishi, Y ;
Ohtsubo, T ;
Sakumi, K ;
Nakabeppu, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (40) :38121-38124
[7]   Characterization of the genomic structure and expression of the mouse Apex2 gene [J].
Ide, Y ;
Tsuchimoto, D ;
Tominaga, Y ;
Iwamoto, Y ;
Nakabeppu, Y .
GENOMICS, 2003, 81 (01) :47-57
[8]   Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C→T:A mutations [J].
Jones, S ;
Emmerson, P ;
Maynard, J ;
Best, JM ;
Jordan, S ;
Williams, GT ;
Sampson, JR ;
Cheadle, JP .
HUMAN MOLECULAR GENETICS, 2002, 11 (23) :2961-2967
[9]   INTRACELLULAR-LOCALIZATION OF 8-OXO-DGTPASE IN HUMAN-CELLS, WITH SPECIAL REFERENCE TO THE ROLE OF THE ENZYME IN MITOCHONDRIA [J].
KANG, D ;
NISHIDA, J ;
IYAMA, A ;
NAKABEPPU, Y ;
FURUICHI, M ;
FUJIWARA, T ;
SEKIGUCHI, M ;
TAKESHIGE, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14659-14665
[10]   Hypoxia induces mitochondrial DNA damage and stimulates expression of a DNA repair enzyme, the Escherichia coli MutY DNA glycosylase homolog (MYH), in vivo, in the rat brain [J].
Lee, HM ;
Wang, C ;
Hu, ZY ;
Greeley, GH ;
Makalowski, W ;
Hellmich, HL ;
Englander, EW .
JOURNAL OF NEUROCHEMISTRY, 2002, 80 (05) :928-937