Expression of transmembrane serine protease TMPRSS2 in mouse and human tissues

The purpose of this study was to clarify the expression of TMPRSS2 in mice during development and to compare the tissue distribution of the transcripts in adult mouse and human tissues. Mouse TMPRSS2 cDNA was cloned; the predicted amino acid sequence contains 490 residues sharing 81.4% similarity wi...

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Published inThe Journal of pathology Vol. 193; no. 1; pp. 134 - 140
Main Authors Vaarala, Markku H., Porvari, Katja S., Kellokumpu, Sakari, Kyllönen, Atte P., Vihko, Pirkko T.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.01.2001
Wiley
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Summary:The purpose of this study was to clarify the expression of TMPRSS2 in mice during development and to compare the tissue distribution of the transcripts in adult mouse and human tissues. Mouse TMPRSS2 cDNA was cloned; the predicted amino acid sequence contains 490 residues sharing 81.4% similarity with human TMPRSS2. According to northern blots, mouse TMPRSS2 is expressed mainly in the prostate and kidney, while human TMPRSS2 is expressed in the prostate, colon, stomach, and salivary gland. In situ hybridization analyses of mouse embryos and adult tissues revealed that TMPRSS2 was expressed in the epithelia of the gastrointestinal, urogenital, and respiratory tracts. Expression was very selective and constant after the gene was turned on during development. Expression of TMPRSS2 was localized in the luminal epithelial cells of the mouse and human prostate. The information presented here will be useful in further studies regarding the function and physiological significance of TMPRSS2. Copyright © 2000 John Wiley & Sons, Ltd.
Bibliography:Finnish Cancer Foundation
istex:DF4A7DF0986C72F13A04238E051EEBBF22D8290C
ArticleID:PATH743
Research Council for Health, Academy of Finland - No. 3314; No. 40990
Ministries of Education, Social Affairs and Health, and Foreign Affairs Finland
ark:/67375/WNG-L84L34G1-Z
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-3417
1096-9896
DOI:10.1002/1096-9896(2000)9999:9999<::AID-PATH743>3.0.CO;2-T