Abdelgadir S E, Roselli C E, Choate J V, Resko J A
Department of Physiology and Pharmacology, School of Medicine, Oregon Health Sciences University, Portland 97201-3098, USA.
Biol Reprod. 1997 Oct;57(4):772-7. doi: 10.1095/biolreprod57.4.772.
The conversion of androgens to estrogens by aromatase cytochrome P450 (P450arom) is an important step in the mechanism of androgen action in the brain. However, the distribution of P450arom mRNA in adult rhesus monkey brains has not been studied because specific probes have not been available. To address this deficit, we cloned and sequenced a 455-basepair segment of the 5' coding region of the rhesus P450arom cDNA. Total RNA was extracted from a rhesus monkey placenta (Day 47 of gestation and subjected to reverse transcriptase (RT) polymerase chain reaction (PCR) using consensus oligonucleotide primers selected from published human and rat P450arom DNA sequences. The RT-PCR product was subcloned into a vector and sequenced. The monkey P450arom cDNA was 97% identical to the human sequence but shared only 86% homology with the rat sequence. We then developed a ribonuclease protection assay using a monkey P450arom cDNA and studied the distribution of P450arom mRNA in adult monkey brains. This assay protected two RNA fragments, one 455 nucleotides (nt) in length and the second approximately 300 nt. The relative distribution of P450arom mRNA (the 455-nt fragment) between brain areas of the adult (n = 3) was high in the bed nucleus of the stria terminalis > medial preoptic/anterior hypothalamus > amygdala; intermediate in the medial basal hypothalamus (infundibular nucleus, median eminence, ventromedial nucleus) > lateral preoptic/anterior hypothalamus; and low in the septum > lateral-dorsal-medial hypothalamus. P450arom mRNA was undetectable in cingulate and parietal cortex, hippocampus, and cerebellum. P450arom activity, as measured by the 3H2O assay, correlated well with the distribution of P450arom mRNA (the 455-nt protected fragment; r = 0.9) in the same tissues. A shorter protected RNA fragment was found in the medial basal hypothalamus, the bed nucleus of the stria terminalis, the amygdala, and the cingulate and parietal cortex but not in the other brain areas investigated. Its presence did not correlate with aromatase activity in brain tissue. This study describes the development of a ribonuclease protection assay using a monkey cDNA produced by RT-PCR and its usefulness for studying the distribution of P450arom mRNA in brains of nonhuman primates.
细胞色素P450芳香化酶(P450arom)将雄激素转化为雌激素是雄激素在大脑中发挥作用机制的重要一步。然而,由于缺乏特异性探针,尚未对成年恒河猴大脑中P450arom mRNA的分布进行研究。为解决这一不足,我们克隆并测序了恒河猴P450arom cDNA 5'编码区的一个455个碱基对的片段。从恒河猴胎盘(妊娠第47天)提取总RNA,使用从已发表的人类和大鼠P450arom DNA序列中选择的共有寡核苷酸引物进行逆转录酶(RT)聚合酶链反应(PCR)。RT-PCR产物亚克隆到载体中并测序。恒河猴P450arom cDNA与人类序列的同源性为97%,但与大鼠序列的同源性仅为86%。然后,我们使用恒河猴P450arom cDNA开发了一种核糖核酸酶保护试验,并研究了成年猴大脑中P450arom mRNA的分布。该试验可保护两个RNA片段,一个长度为455个核苷酸(nt),另一个约为300 nt。成年猴(n = 3)脑区之间P450arom mRNA(455-nt片段)的相对分布在终纹床核>内侧视前区/下丘脑前部>杏仁核中较高;在内侧基底下丘脑(漏斗核、正中隆起、腹内侧核)>外侧视前区/下丘脑前部中中等;在隔区>外侧-背侧-内侧下丘脑区中较低。在扣带回和顶叶皮质、海马体和小脑中未检测到P450arom mRNA。通过3H2O试验测量的P450arom活性与相同组织中P450arom mRNA(受保护的455-nt片段;r = 0.9)的分布密切相关。在内侧基底下丘脑、终纹床核、杏仁核以及扣带回和顶叶皮质中发现了一个较短的受保护RNA片段,但在其他研究的脑区中未发现。它的存在与脑组织中的芳香化酶活性无关。本研究描述了使用RT-PCR产生的恒河猴cDNA开发的核糖核酸酶保护试验及其在研究非人灵长类动物大脑中P450arom mRNA分布方面的用途。