Dalla Valle L, Couët J, Labrie Y, Simard J, Belvedere P, Simontacchi C, Labrie F, Colombo L
Department of Biology, University of Padova, Italy.
Mol Cell Endocrinol. 1995 Apr 28;111(1):83-92. doi: 10.1016/0303-7207(95)03553-j.
We have investigated 17 alpha-hydroxylase and C17,20-lyase activities and the presence of cytochrome P450c17 mRNA in the esophagus, stomach, duodenum, and colon of adult rats of both sexes. All tissues converted [4-14C]pregnenolone mainly to dehydroepiandrosterone (DHEA) through the 5-ene-3 beta-hydroxysteroid route as opposed to the 4-ene-3-ketosteroid pathway in a control testicular incubate. Synthesis of dehydroepiandrosterone was particularly high in the duodenum and was found to be lower in the stomach, colon and esophagus, in decreasing order. 20 alpha-Hydroxypregnenolone and progesterone were also formed primarily by the esophagus and colon, respectively. P450c17 mRNA was demonstrated by ribonuclease protection assay in the stomach and duodenum, but not in esophagus and colon. However, a 335 bp-long cDNA fragment, whose sequence corresponded to that of rat P450c17 cDNA, was amplified by reverse transcription (RT) and polymerase chain reaction (PCR) from the poly(A)+ RNAs of all four tissues. This result was further confirmed by Southern blotting using a 794-bp testicular probe. The complete sequence of P450c17 cDNA in the stomach and duodenum was identical to that reported for rat testis P450c17 cDNA. No amplification and no positive signal in Southern blotting were observed with the total RNAs from adult male adrenal and spleen, which were taken as negative controls since they had been previously found unable to form androgens from pregnenolone. Although the levels of transcription in gonads, duodenum and stomach were found to be equivalent, as indicated by the RNase protection assay and semiquantitative RT-PCR assay, P450c17 enzyme activity was much higher in the testis, pointing at a possible dissimilarity in the respective rates of mRNA translation. Thus, P450c17 is differentially expressed in the rat gastrointestinal tract, where it leads to the synthesis of the sex steroid precursor DHEA, especially in the duodenum and stomach.
我们研究了成年雌雄大鼠食管、胃、十二指肠和结肠中17α-羟化酶和C17,20-裂解酶的活性以及细胞色素P450c17 mRNA的存在情况。与对照睾丸孵育物中通过4-烯-3-酮类固醇途径不同,所有组织均通过5-烯-3β-羟类固醇途径将[4-14C]孕烯醇酮主要转化为脱氢表雄酮(DHEA)。脱氢表雄酮的合成在十二指肠中特别高,在胃、结肠和食管中依次降低。20α-羟孕烯醇酮和孕酮也分别主要由食管和结肠形成。通过核糖核酸酶保护试验在胃和十二指肠中检测到P450c17 mRNA,但在食管和结肠中未检测到。然而,通过逆转录(RT)和聚合酶链反应(PCR)从所有四个组织的聚腺苷酸(poly(A)+)RNA中扩增出一个335 bp长的cDNA片段,其序列与大鼠P450c17 cDNA的序列一致。使用794 bp睾丸探针进行的Southern印迹进一步证实了这一结果。胃和十二指肠中P450c17 cDNA的完整序列与报道的大鼠睾丸P450c17 cDNA的序列相同。以成年雄性肾上腺和脾脏的总RNA作为阴性对照,未观察到扩增和Southern印迹阳性信号,因为先前发现它们无法从孕烯醇酮形成雄激素。尽管核糖核酸酶保护试验和半定量RT-PCR试验表明性腺、十二指肠和胃中的转录水平相当,但睾丸中P450c17酶活性要高得多,这表明mRNA翻译的各自速率可能存在差异。因此,P450c17在大鼠胃肠道中差异表达,在那里它导致性类固醇前体DHEA的合成,特别是在十二指肠和胃中。