Meyerhof W, Paust H J, Schönrock C, Richter D
Institut für Zellbiochemie und klinische Neurobiologie, UKE, Hamburg, FRG.
DNA Cell Biol. 1991 Nov;10(9):689-94. doi: 10.1089/dna.1991.10.689.
A cDNA clone encoding a novel putative G-protein-coupled receptor was isolated from a rat brain cDNA library using a PCR-amplified cDNA fragment as a hybridization probe. The 3,615-bp-long nucleotide sequence predicts a single open reading frame of 1,173 bp coding for 391 amino acids, giving a calculated molecular weight of 42.75 kD. The amino acid sequence shares features common to many other receptors, including the seven membrane-spanning hydrophobic regions and putative asparagine-linked glycosylation and phosphorylation sites. Northern blot analysis reveals that a corresponding approximately 3.7-kb mRNA is expressed in specific brain regions such as hypothalamus, cortex, hippocampus, and thalamus but not in other organs analyzed. Although the ligand for this receptor has not yet been identified, it shares some similarities with the vascular type-1 angiotensin II receptor, the vasoactive intestinal peptide (VIP) receptor, and the chemotactic receptors for human C5a anaphylatoxin and the formyl peptide fMet-Leu-Phe.
利用PCR扩增的cDNA片段作为杂交探针,从大鼠脑cDNA文库中分离出一个编码新型假定G蛋白偶联受体的cDNA克隆。3615bp长的核苷酸序列预测有一个1173bp的单一开放阅读框,编码391个氨基酸,计算分子量为42.75kD。该氨基酸序列具有许多其他受体共有的特征,包括七个跨膜疏水区域以及假定的天冬酰胺连接的糖基化和磷酸化位点。Northern印迹分析显示,相应的约3.7kb mRNA在下丘脑、皮层、海马体和丘脑等特定脑区表达,但在分析的其他器官中不表达。虽然该受体的配体尚未确定,但它与血管1型血管紧张素II受体、血管活性肠肽(VIP)受体以及人C5a过敏毒素和甲酰肽fMet-Leu-Phe的趋化受体有一些相似之处。