Hinshelwood M M, Liu Z, Conley A J, Simpson E R
Cecil H. and Ida Green Center for Reproductive Biology Sciences, Department of Biochemistry and Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas 75235-9051, USA.
Biol Reprod. 1995 Nov;53(5):1151-9. doi: 10.1095/biolreprod53.5.1151.
Conversion of androgens to estrogens is catalyzed by aromatase P450 (P450arom; the product of the CYP19 gene). Regulation of tissue-specific expression of P450arom in humans is due, in part, to alternative transcriptional start sites that arise as a consequence of the use of granulosa cells and placental tissue from cows, horses, and pigs (ungulates) in order to determine whether these species, like the human, utilize tissue-specific promoters to drive P450arom expression. The majority of transcripts in the placenta have 5'-termini that differ from those in the ovary upstream of a common site of divergence, indicative of a splice junction. The use of tissue-specific promoters by the bovine CYP19 gene would produce these results, as it does in the case of the human CYP19 gene. A bovine genomic library was then screened with probes that hybridize to ovary- or placenta-specific transcripts. Two clones of approximately 15 kb each in length were isolated; one hybridized with the ovary-specific sequence and the other hybridized with the placenta-specific sequence. Whereas the former sequence was contiguous with the downstream sequence containing the translational start site, the latter was identical only with the sequence of the placental transcripts upstream of the putative splice junction, indicating that this was the distal sequence. Bovine and human ovary-specific genomic sequences share 77% bp identity, while bovine and human placenta-specific sequences demonstrated only 39% bp identity. These results mirror those obtained in comparisons of human, bovine, equine, and porcine ovarian and placental RACE cDNA 5'-termini.(ABSTRACT TRUNCATED AT 250 WORDS)
雄激素向雌激素的转化由芳香化酶P450(P450arom;CYP19基因的产物)催化。人类P450arom组织特异性表达的调控部分归因于替代转录起始位点,这些位点是由于使用牛、马和猪(有蹄类动物)的颗粒细胞和胎盘组织而产生的,目的是确定这些物种是否像人类一样利用组织特异性启动子来驱动P450arom表达。胎盘中的大多数转录本具有与卵巢中共同分歧位点上游的转录本不同的5'-末端,这表明存在一个剪接连接点。牛CYP19基因使用组织特异性启动子会产生这些结果,就像人类CYP19基因的情况一样。然后用与卵巢或胎盘特异性转录本杂交的探针筛选牛基因组文库。分离出两个长度约为15 kb的克隆;一个与卵巢特异性序列杂交,另一个与胎盘特异性序列杂交。前者序列与包含翻译起始位点的下游序列相邻,而后者仅与推定剪接连接点上游的胎盘转录本序列相同,这表明这是远端序列。牛和人类卵巢特异性基因组序列的碱基同一性为77%,而牛和人类胎盘特异性序列的碱基同一性仅为39%。这些结果与在人类、牛、马和猪卵巢及胎盘RACE cDNA 5'-末端比较中获得的结果相似。(摘要截短于250字)