Clerch L B, Wright A, Slobodyansky E, Wang W, Mouradian M M, Jose P
Georgetown University Medical Center, Department of Pediatrics, Washington, DC 20007, USA.
Clin Exp Hypertens. 1997 Oct;19(7):1009-21. doi: 10.3109/10641969709083202.
Rat kidney extracts contain a 52 kDa protein that binds to the 3' untranslated region of the dopamine 1A (D1A) receptor mRNA at a 243 base-long cis element starting at the stop codon and ending approximately 220 bases upstream of an AUUUA-rich region. The D1A receptor RNA-binding protein (D1A-BP) is redox-sensitive; free sulfhydryl groups on the protein are required for binding. Kidney extracts from SHR have significantly more D1A-BP activity than extracts from WKY rats. When kidney extracts were tested for binding to an 80-base RNA containing four AUUUA repeats, there was also greater binding activity in extracts from SHR. These increases are at least partly specific because there was no difference in catalase RNA-binding protein activity between the two rat strains. These data suggest D1A-BP and AUUUA-binding protein may play a role in posttranscriptional regulation of the D1A receptor in the hypertensive rat.
大鼠肾脏提取物含有一种52 kDa的蛋白质,该蛋白质在一个从终止密码子开始、在富含AUUUA的区域上游约220个碱基处结束的243个碱基长的顺式元件上,与多巴胺1A(D1A)受体mRNA的3'非翻译区结合。D1A受体RNA结合蛋白(D1A-BP)对氧化还原敏感;蛋白质上的游离巯基是结合所必需的。自发性高血压大鼠(SHR)的肾脏提取物比WKY大鼠的提取物具有显著更多的D1A-BP活性。当检测肾脏提取物与含有四个AUUUA重复序列的80碱基RNA的结合时,SHR的提取物中也有更高的结合活性。这些增加至少部分是特异性的,因为两种大鼠品系之间的过氧化氢酶RNA结合蛋白活性没有差异。这些数据表明,D1A-BP和AUUUA结合蛋白可能在高血压大鼠D1A受体的转录后调控中发挥作用。