Molecular cloning and tissue-specific expression of Mrad9, a murine orthologue of the Schizosaccharomyces pombe rad9+ checkpoint control gene

We have isolated a murine cDNA, Mrad9, that is orthologous to the fission yeast rad9+ and human HRAD9 genes. Mrad9 encodes a 389 amino acid long, 42,032 Dalton protein that is 27% identical and 56% similar to Rad9p, and 82% identical and 88% similar to HRAD9, at the amino acid level. Expression of t...

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Published inJournal of cellular physiology Vol. 177; no. 2; pp. 241 - 247
Main Authors Hang, Haiying, Rauth, Sarah J., Hopkins, Kevin M., Davey, Scott K., Lieberman, Howard B.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.11.1998
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Summary:We have isolated a murine cDNA, Mrad9, that is orthologous to the fission yeast rad9+ and human HRAD9 genes. Mrad9 encodes a 389 amino acid long, 42,032 Dalton protein that is 27% identical and 56% similar to Rad9p, and 82% identical and 88% similar to HRAD9, at the amino acid level. Expression of the Mrad9 cDNA in Schizosaccharomyces pombe rad9::ura4+ cells restores nearly wild‐type levels of hydroxyurea resistance and early S phase checkpoint control to mutant fission yeast cell populations. However, UV resistance is only minimally restored, and mutant cells remain sensitive to gamma radiation. Mrad9 genomic DNA was isolated from a mouse 129/SvEv library. The Mrad9 gene was localized to a 15‐kbp genomic DNA fragment, and contains 10 exons separated by 9 introns. Northern blot analysis indicates that the gene is expressed in many different tissues of the adult mouse, but the mRNA is most abundant in the heart and present at very low levels in the liver. These studies demonstrate the existence of a murine orthologue of the fission yeast rad9+ gene and underscore at least the partial evolutionary conservation of rad9+‐dependent checkpoint control mechanisms. J. Cell. Physiol. 177:241–247, 1998. © 1998 Wiley‐Liss, Inc.
Bibliography:Cancer Care Ontario - No. MT-14352
istex:62B8A8925FA4F8F9DD08CCA28CDFE56810A61359
DOE - No. DE-FG07-96ER62309
ArticleID:JCP6
NIH - No. GM52493; No. CA68446
ark:/67375/WNG-WN4B07FD-X
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0021-9541
1097-4652
DOI:10.1002/(SICI)1097-4652(199811)177:2<241::AID-JCP6>3.0.CO;2-N