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J Biol Chem, Vol. 273, Issue 8, 4574-4584, February 20, 1998
,
§
From the § Department of Cell Biology and the
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.
Cell and Molecular Biology Program, Baylor College of
Medicine, Houston, Texas 77030
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