JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Larsen, M.
Right arrow Articles by Rowley, D. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Larsen, M.
Right arrow Articles by Rowley, D. R.

J Biol Chem, Vol. 273, Issue 8, 4574-4584, February 20, 1998

Molecular Cloning and Expression of ps20 Growth Inhibitor
A NOVEL WAP-TYPE "FOUR-DISULFIDE CORE" DOMAIN PROTEIN EXPRESSED IN SMOOTH MUSCLE

Melinda LarsenDagger , Steven J. Ressler§, Bing Lu§, Michael J. Gerdes§, Lauren McBride§, Truong D. Dang§, and David R. RowleyDagger §

From the § Department of Cell Biology and the Dagger  Cell and Molecular Biology Program, Baylor College of Medicine, Houston, Texas 77030

We previously reported the purification of ps20 (Rowley, D. R., Dang, T. D., Larsen, M., Gerdes, M. J., McBride, L., and Lu, B. (1995) J. Biol. Chem. 270, 22058-22065), a urogenital sinus mesenchymal cell secreted protein having growth-inhibitory properties. We report here cloning of the 1.03-kilobase rat ps20 cDNA clone from the PS-1 (adult rat prostate smooth muscle) cDNA library. Partial clones were obtained by nested polymerase chain reaction with degenerate primers, and full-length ps20 cDNA clones were isolated by plaque hybridization. Sequence analysis revealed that ps20 protein contains a WAP-type "four-disulfide core" motif and is a novel member of the WAP signature protein family composed primarily of secreted serine protease inhibitors. Native ps20 immunoprecipitated from smooth muscle cells and recombinant ps20 both resolved on SDS-polyacrylamide gel electrophoresis with apparent molecular mass of 27-29 kDa under reducing conditions and 21-23 kDa under non-reducing conditions, respectively. Stable ps20-transfectant COS-7 cell lines secreted ps20 and were growth-inhibited relative to mock transfectants. In addition, COS-7 and prostate carcinoma PC-3 cells were growth-inhibited by bacterially expressed ps20. Northern analysis indicated differential expression by tissue with highest expression in the heart. Immunohistochemical localization of ps20 protein showed cell-specific expression by both visceral and vascular smooth muscle in all tissues, including the prostate gland. These results indicate ps20 is a novel growth-regulatory member of the WAP signature family expressed by smooth muscle cells.


Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.



This article has been cited by other articles:


Home page
J. Virol.Home page
R. Alvarez, J. Reading, D. F. L. King, M. Hayes, P. Easterbrook, F. Farzaneh, S. Ressler, F. Yang, D. Rowley, and A. Vyakarnam
WFDC1/ps20 Is a Novel Innate Immunomodulatory Signature Protein of Human Immunodeficiency Virus (HIV)-Permissive CD4+ CD45RO+ Memory T Cells That Promotes Infection by Upregulating CD54 Integrin Expression and Is Elevated in HIV Type 1 Infection
J. Virol., January 1, 2008; 82(1): 471 - 486.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Y. Furutani, A. Kato, A. Fibriani, T. Hirata, R. Kawai, J.-H. Jeon, Y. Fujii, I.-G. Kim, S. Kojima, and S. Hirose
Identification, Evolution, and Regulation of Expression of Guinea Pig Trappin with an Unusually Long Transglutaminase Substrate Domain
J. Biol. Chem., May 27, 2005; 280(21): 20204 - 20215.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
H. Hung
Suppression of ps20 Expression in the Rat Uterus by Tamoxifen and Estrogens
Endocrinology, May 1, 2005; 146(5): 2388 - 2396.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
L.M. Helvering, M.D. Adrian, A.G. Geiser, S.T. Estrem, T. Wei, S. Huang, P. Chen, E.R. Dow, J. N. Calley, J.A. Dodge, et al.
Differential Effects of Estrogen and Raloxifene on Messenger RNA and Matrix Metalloproteinase 2 Activity in the Rat Uterus
Biol Reprod, April 1, 2005; 72(4): 830 - 841.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
H. Endoh, S. Tomida, Y. Yatabe, H. Konishi, H. Osada, K. Tajima, H. Kuwano, T. Takahashi, and T. Mitsudomi
Prognostic Model of Pulmonary Adenocarcinoma by Expression Profiling of Eight Genes As Determined by Quantitative Real-Time Reverse Transcriptase Polymerase Chain Reaction
J. Clin. Oncol., March 1, 2004; 22(5): 811 - 819.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
S. J. McAlhany, S. J. Ressler, M. Larsen, J. A. Tuxhorn, F. Yang, T. D. Dang, and D. R. Rowley
Promotion of Angiogenesis by ps20 in the Differential Reactive Stroma Prostate Cancer Xenograft Model
Cancer Res., September 15, 2003; 63(18): 5859 - 5865.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
M. J. Gerdes, T. D. Dang, M. Larsen, and D. R. Rowley
Transforming Growth Factor-{beta}1 Induces Nuclear to Cytoplasmic Distribution of Androgen Receptor and Inhibits Androgen Response in Prostate Smooth Muscle Cells
Endocrinology, August 1, 1998; 139(8): 3569 - 3577.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. J. Simpson, S. Ranganathan, J. A. Fisher, P. A. Janssens, D. C. Shaw, and K. R. Nicholas
The Gene for a Novel Member of the Whey Acidic Protein Family Encodes Three Four-disulfide Core Domains and Is Asynchronously Expressed during Lactation
J. Biol. Chem., July 21, 2000; 275(30): 23074 - 23081.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1998 by the American Society for Biochemistry and Molecular Biology.