Orwig K E, Dai G, Rasmussen C A, Soares M J
Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City 66160, USA.
Endocrinology. 1997 Jun;138(6):2491-500. doi: 10.1210/endo.138.6.5155.
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 [17.7 kilobases (kb)] and RGLd-42 (15.8 kb). RGLd-41 alone was found to contain the full-length 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 5'-flanking region.
蜕膜/滋养层催乳素相关蛋白(d/tPRP)是催乳素基因家族的成员之一,在孕期以高度协调的模式在子宫和胎盘组织中双重表达。在本研究中,我们描述了d/tPRP基因的分离与特性。用标记的d/tPRP互补DNA筛选λDASH II Wistar-Kyoto大鼠基因组文库,分离出两个噬菌体克隆,RGLd-41[17.7千碱基(kb)]和RGLd-42(15.8 kb)。发现仅RGLd-41包含全长d/tPRP基因,并用于后续分析。d/tPRP基因具有六个外显子、五个内含子的结构。相对于催乳素基因家族的其他高度保守成员,d/tPRP在典型催乳素基因的外显子2和3之间含有一个额外的小外显子(外显子3)。与d/tPRP外显子3对应的区域编码催乳素家族成员亚群中发现的一个独特氨基酸区域。对d/tPRP信使RNA进行逆转录聚合酶链反应(RT-PCR)组织检测显示,d/tPRP表达仅限于蜕膜和滋养层组织。在蜕膜组织中,在起始密码子上游65 bp处鉴定出一个单一转录起始位点,而在胎盘组织中,在起始密码子上游61 - 66 bp范围内检测到多个转录起始位点。对各种组织培养系统(原代培养物和细胞系)进行d/tPRP表达和3.96 kb d/tPRP启动子-荧光素酶报告构建体激活的评估。蜕膜、海绵滋养层和滋养层巨细胞群体表达d/tPRP,并能够激活d/tPRP启动子-报告构建体,而其他细胞类型则无效。在子宫基质细胞系中观察到有限的d/tPRP启动子激活。总之,d/tPRP具有独特的六个外显子、五个内含子基因结构,并表现出细胞特异性表达,其至少部分受3.96 kb 5'侧翼区域调控。