Neill J D, Musgrove L C, Sellers J C, Duck L W
Department of Physiology and Biophysics, Schools of Medicine and Dentistry, University of Alabama at Birmingham 35294, USA.
Endocrinology. 1996 Sep;137(9):3942-7. doi: 10.1210/endo.137.9.8756570.
G protein-coupled receptor kinases (GRK 1-6) stimulate short-term desensitization (< 5 min) by phosphorylating G-protein coupled receptors, and also participate in receptor sequestration, which may relate to intermediate-term desensitization (30-60 min). The existence of such kinases and hence a potential role for them in gonadotrope/GnRH receptor desensitization was investigated using the PCR to identify GRKs in messenger RNA (mRNA) from the mouse alpha T3-1 gonadotrope cell line. The 150-bp complementary DNAs amplified by PCR from the kinase catalytic domain were cloned and sequenced. Seventeen of 42 clones were receptor kinases based on high nucleotide identities of 85-100% and amino acid identities of 97-100% with rat GRK2 and 3, and with human GRK6. Among the eight GRK3 clones was one differing from rat GRK3 by a single nucleotide and seven differing by six; no amino acid difference resulted from the nucleotide differences. Of the five GRK2 clones, one sequence was identical with rat GRK2, but four sequences differed by three nucleotides and one amino acid. Among four GRK6 sequences, one showed 15 nucleotide differences from human GRK6 (with no amino acid differences), and three had 16 nucleotide and one amino acid differences. For each of the three GRKs found, the most closely related isoform is assumed to be the mouse homolog of rat GRK2 and GRK3, and human GRK6, whereas the others are assumed to be previously undescribed isoforms or subtypes of GRK2, 3, and 6. Immunocytochemical staining using antibodies to GRK2, 3, and 6 confirmed their presence in alpha T3-1 cells. The function of these GRKs in alpha T3-1 cells is unknown, but they may be involved in short-term desensitization of the gonadotrope/GnRH receptor or perhaps, more likely, the sequestration of this receptor during intermediate-term desensitization.
G蛋白偶联受体激酶(GRK 1 - 6)通过磷酸化G蛋白偶联受体来刺激短期脱敏(<5分钟),并且还参与受体隔离,这可能与中期脱敏(30 - 60分钟)有关。利用聚合酶链反应(PCR)从小鼠αT3 - 1促性腺激素细胞系的信使核糖核酸(mRNA)中鉴定GRK,研究了此类激酶的存在及其在促性腺激素细胞/促性腺激素释放激素(GnRH)受体脱敏中的潜在作用。通过PCR从激酶催化结构域扩增得到的150个碱基对的互补DNA被克隆并测序。基于与大鼠GRK2和3以及人类GRK6的85 - 100%的高核苷酸同一性和97 - 100%的氨基酸同一性,42个克隆中有17个是受体激酶。在8个GRK3克隆中,有1个与大鼠GRK3仅相差1个核苷酸,7个相差6个;核苷酸差异未导致氨基酸差异。在5个GRK2克隆中,1个序列与大鼠GRK2相同,但4个序列相差3个核苷酸和1个氨基酸。在4个GRK6序列中,1个与人类GRK6有15个核苷酸差异(无氨基酸差异),3个有16个核苷酸和1个氨基酸差异。对于发现的三种GRK中的每一种,最密切相关的亚型被认为是大鼠GRK2和GRK3以及人类GRK6的小鼠同源物,而其他的则被认为是GRK2、3和6以前未描述的亚型。使用针对GRK2、3和6的抗体进行免疫细胞化学染色证实了它们在αT3 - 1细胞中的存在。这些GRK在αT3 - 1细胞中的功能尚不清楚,但它们可能参与促性腺激素细胞/GnRH受体的短期脱敏,或者更有可能参与中期脱敏期间该受体的隔离。