Clarke D L, Linzer D I
Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, Illinois 60208.
Endocrinology. 1993 Jul;133(1):224-32. doi: 10.1210/endo.133.1.8319571.
We have isolated the cDNA encoding the cytoplasmic domain of a long form of the mouse PRL receptor (PRL-R). The mRNA for this long form PRL-R and the three mRNAs encoding short mouse PRL-R that have been previously characterized are all expressed in both the liver and ovary. The relative amounts of these receptor forms differ between tissues, however. In addition, the structure of one of the short receptor forms may not be identical in the liver and ovary. Within the ovary, the abundance and sites of synthesis of the four PRL-R mRNAs vary during pregnancy. Expression of the two most abundant PRL-R mRNAs increases significantly at midgestation. Expression of PRL-R mRNA is detected in the corpus luteum throughout pregnancy, while increased receptor mRNA levels are evident in the granulosa cells of a subset of Graafian follicles toward the end of pregnancy and during lactation. Some differences are also observed in the expression patterns of the individual receptor forms. Most notably, one of the short form PRL-R mRNAs is uniquely detected in atretic follicles in early to midgestation.
我们已经分离出编码小鼠催乳素受体(PRL-R)长形式胞质结构域的cDNA。这种长形式PRL-R的mRNA以及先前已鉴定的三种编码小鼠PRL-R短形式的mRNA在肝脏和卵巢中均有表达。然而,这些受体形式的相对含量在不同组织之间存在差异。此外,其中一种短受体形式的结构在肝脏和卵巢中可能并不相同。在卵巢内,四种PRL-R mRNA的丰度和合成位点在妊娠期间会发生变化。两种最丰富的PRL-R mRNA的表达在妊娠中期显著增加。在整个妊娠期间,黄体中均可检测到PRL-R mRNA的表达,而在妊娠末期和哺乳期,一部分格拉夫卵泡的颗粒细胞中受体mRNA水平明显升高。在各个受体形式的表达模式中也观察到了一些差异。最值得注意的是,在妊娠早期至中期的闭锁卵泡中独特地检测到一种短形式PRL-R mRNA。