Kurihara T, Lewis R M, Eisler J, Greengard P
Laboratory of Molecular and Cellular Neuroscience, Rockefeller University, New York, New York 10021.
J Neurosci. 1988 Feb;8(2):508-17. doi: 10.1523/JNEUROSCI.08-02-00508.1988.
A cDNA clone for the mRNA of bovine DARPP-32 (dopamine- and adenosine 3',5'-monophosphate-regulated phosphoprotein, Mr = 32,000) was isolated from a modified Okayama-Berg plasmid library. Transformed Escherichia coli colonies were screened by in situ colony hybridization with 2 different oligonucleotide probes corresponding to a region unusually rich in glutamate within the protein. Three positive clones were isolated and shown to encode DARPP-32 by an in situ immunoblot assay of their fusion protein products with beta-galactosidase. The results of the sequence analysis of the longest cDNA clone, pTKD7 (1771 nucleotides), revealed a 606-nucleotide-long coding region, in exact agreement with the bovine DARPP-32 amino acid sequence (Williams et al., 1986). Southern blot analysis of total bovine genomic DNA showed that there is a single gene coding for DARPP-32. Northern blot analysis of caudate nucleus RNA using antisense RNA derived from the clone pTKD7 demonstrated the existence of 2 abundant mRNA species, corresponding to 1.8 and 1.65 kilobase in length. The high concentration of DARPP-32 mRNAs in the caudate nucleus is in agreement with the known distribution of this protein.
从改良的冈山县-伯格质粒文库中分离出牛DARPP-32(多巴胺和3',5'-单磷酸腺苷调节的磷蛋白,分子量=32,000)mRNA的cDNA克隆。用两种不同的寡核苷酸探针通过原位菌落杂交筛选转化的大肠杆菌菌落,这两种探针对应于该蛋白中一个谷氨酸异常丰富的区域。分离出三个阳性克隆,并通过对其与β-半乳糖苷酶的融合蛋白产物进行原位免疫印迹分析,证明它们编码DARPP-32。最长的cDNA克隆pTKD7(1771个核苷酸)的序列分析结果显示,其编码区长度为606个核苷酸,与牛DARPP-32氨基酸序列完全一致(Williams等人,1986年)。对牛基因组总DNA的Southern印迹分析表明,存在一个编码DARPP-32的单一基因。使用来自克隆pTKD7的反义RNA对尾状核RNA进行Northern印迹分析,结果显示存在两种丰富的mRNA种类,长度分别对应1.8和1.65千碱基。尾状核中DARPP-32 mRNA的高浓度与该蛋白的已知分布一致。