Decidual/trophoblast prolactin-related protein: Characterization of gene structure and cell-specific expression

被引:41
作者
Orwig, KE [1 ]
Dai, GL [1 ]
Rasmussen, CA [1 ]
Soares, MJ [1 ]
机构
[1] UNIV KANSAS, MED CTR, DEPT PHYSIOL, DEPT MOL & INTEGRAT PHYSIOL, KANSAS CITY, KS 66160 USA
关键词
D O I
10.1210/en.138.6.2491
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Decidual/trophoblast PRL-related protein (d/tPRP) is a member of the PRL gene family and is dually expressed in uterine and placental tissues in a highly coordinated pattern during pregnancy. In the present study, we describe the isolation and characterization of the d/tPRP gene. A lambda DASH II Wistar-Kyoto rat genomic library was screened with a labeled d/tPRP complementary DNA, resulting in the isolation of two phage clones, RGLd-41 117.7 kilobases (kb)] and RGLd-42 (15.8 kb). RGLd-41 alone was found to contain the fulllength d/tPRP gene and was used for subsequent analyses. The d/tPRP gene possesses a six-exon, five-intron organization. Relative to other highly conserved members of the PRL gene family, d/tPRP contains a single small additional exon (exon 3) situated between exons 2 and 3 of the prototypical PRL gene. The region corresponding to exon 3 of d/tPRP encodes for a unique amino acid region found in a subset of PRL family members. A reverse transcription-PCR (RT-PCR) tissue survey for d/tPRP messenger RNA revealed that d/tPRP expression was restricted to decidual and trophoblast tissues. A single transcription start site 65 bp upstream of the initiation codon was identified in decidual tissue, whereas multiple transcription start sites ranging from 61-66 bp upstream of the initiation codon were detected in placental tissue. Various tissue culture systems (primary cultures and cell lines) were evaluated for d/tPRP expression and activation of a 3.96-kb d/tPRP promoter-luciferase reporter construct. Decidual, spongiotrophoblast, and trophoblast giant cell populations expressed d/tPRP and were capable of activating the d/tPRP promoter-reporter construct, whereas other cell types were ineffective. Limited d/tPRP promoter activation was noted in uterine stromal cell lines. In summary, d/tPRP possesses a unique six-exon, five-intron gene structure and exhibits cell-specific expression that is regulated at least in part by a 3.96-kb 6'-flanking region.
引用
收藏
页码:2491 / 2500
页数:10
相关论文
共 64 条
[1]  
ARSLAN A, 1995, IN VITRO CELL DEV-AN, V31, P140
[2]  
Bell S.C., 1983, OXFORD REV REPRODUCT, V5, P220
[3]   CHARACTERIZATION OF AN UP-STREAM PROMOTER DIRECTING EXTRAPITUITARY EXPRESSION OF THE HUMAN PROLACTIN GENE [J].
BERWAER, M ;
MARTIAL, JA ;
DAVIS, JRE .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (05) :635-642
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]  
BRASIER AR, 1989, BIOTECHNIQUES, V7, P1116
[6]   A NOVEL REGULATORY REGION IS REQUIRED FOR TROPHOBLAST-SPECIFIC TRANSCRIPTION IN TRANSGENIC MICE [J].
CALZONETTI, T ;
STEVENSON, L ;
ROSSANT, J .
DEVELOPMENTAL BIOLOGY, 1995, 171 (02) :615-626
[7]   GENOMIC ORGANIZATION OF RAT PROLACTIN AND GROWTH-HORMONE GENES [J].
CHIEN, YH ;
THOMPSON, EB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (08) :4583-4587
[8]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[9]  
COHEN H, 1993, EUR J CELL BIOL, V61, P116
[10]   Placental lactogen-I variant utilizes the prolactin receptor signaling pathway [J].
Cohick, CB ;
Dai, GL ;
Xu, L ;
Deb, S ;
Kamei, T ;
Levan, G ;
Szpirer, C ;
Szpirer, J ;
Kwok, SCM ;
Soares, MJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1996, 116 (01) :49-58