Demmer J
Dairy Science Group, AgResearch, Ruakura Research Centre, Hamilton, New Zealand.
Mol Cell Endocrinol. 1999 Feb 25;148(1-2):119-27. doi: 10.1016/s0303-7207(98)00230-5.
A full length, prolactin receptor cDNA clone has been isolated from the brushtail possum (Trichosurus vulpecula). This clone encodes a 625 amino acid protein which shares 60-70 and 54% sequence identity with prolactin receptor (long form) sequences from mammalian and avian species, respectively. Sequence similarity was highest in the extra-cellular, hormone-binding domain and in specific regions of the intracellular domain which regulates prolactin receptor signalling in cells. Prolactin receptor mRNA was detected in a wide range of possum tissues and in the mammary gland the PRL-R gene was differentially expressed during lactation with peak mRNA levels being detected during the first 6 days of lactation and after day 115 throughout late lactation. This pattern of PRL-R mRNA expression in the mammary gland is similar to that observed for circulating prolactin in the lactating possum. In CHO cells transiently transfected with the possum prolactin receptor, expression of a beta-lactoglobulin promoter/reporter gene construct was increased 3-fold by adding prolactin. The possum prolactin receptor is therefore capable of binding ovine prolactin and activating the Jak2/Stat5 signalling cascade. This provides evidence for the highly conserved nature of the prolactin signalling pathway in mammalian evolution.
已从帚尾袋貂(Trichosurus vulpecula)中分离出一个全长催乳素受体cDNA克隆。该克隆编码一种625个氨基酸的蛋白质,与哺乳动物和鸟类物种的催乳素受体(长形式)序列分别具有60 - 70%和54%的序列同一性。在细胞外激素结合结构域以及调节细胞中催乳素受体信号传导的细胞内结构域的特定区域,序列相似性最高。在袋貂的多种组织中检测到催乳素受体mRNA,在乳腺中,PRL - R基因在哺乳期差异表达,在哺乳期的前6天以及整个哺乳期后期的第115天后检测到mRNA水平峰值。乳腺中PRL - R mRNA的这种表达模式与泌乳袋貂中循环催乳素的表达模式相似。在用袋貂催乳素受体瞬时转染的CHO细胞中,添加催乳素可使β - 乳球蛋白启动子/报告基因构建体的表达增加3倍。因此,袋貂催乳素受体能够结合绵羊催乳素并激活Jak2/Stat5信号级联反应。这为催乳素信号通路在哺乳动物进化中的高度保守性提供了证据。