Choi I, Troyer D L, Cornwell D L, Kirby-Dobbels K R, Collante W R, Simmen F A
Department of Dairy and Poultry Sciences and the Interdisciplinary Concentration in Animal Molecular and Cell Biology, Institute of Food and Agricultural Sciences, University of Florida, Gainesville 32611-0920, USA.
DNA Cell Biol. 1997 Jun;16(6):769-77. doi: 10.1089/dna.1997.16.769.
We examined the chromosomal basis for the synthesis of tissue (ovary, endometrium/placenta, and peri-implantation blastocyst) isoforms of cytochrome P450 aromatase in the pig. DNA fragments derived from three distinct porcine aromatase chromosomal genes were cloned and characterized. The porcine type III aromatase gene encoding the blastocyst aromatase isoform was found to consist of nine coding exons and two mutually exclusive, 5' untranslated exons (designated E1A and E1B), collectively spanning 30 kb or more. The porcine type II aromatase gene, encoding the endometrial/placental aromatase isoform, was identified by cloning of a genomic DNA fragment spanning the corresponding exons 7, 8, and 9. The DNA inserts of two other phage clones encompassed exons 2, 3, and 4 of a third chromosomal gene (type I) encoding the ovarian aromatase isoform. All intron-exon junctions in these genomic fragments were found to be identical in relative positions to those of the single-copy human aromatase gene. Comparisons of cDNA and genomic sequences indicated that nucleotide sequence variation was not uniform across the corresponding exons of these genes and that the corresponding intronic sequences were conserved. The type II and type III aromatase genes were localized to the same regional location (q16-17) on swine chromosome 1, which is homologous to the human chromosome 15 region (q21.1) in which the human aromatase gene resides. Results demonstrate that the three aromatase genes characterized in the present study appear to be similar in their overall structural organization and most likely are clustered, which could have resulted from at least two independent gene duplication events. The presence of multiple aromatase genes constitutes a newly described mechanism by which aromatase enzyme biosynthesis and functional activity can be regulated in a tissue and temporal fashion and serves to highlight further the complexity of aromatase gene expression in mammals. Moreover, the presence of a unique aromatase gene that is highly expressed in pig blastocysts may constitute a paradigm for other mammals (e.g., equids, rabbit, hamster) whose peri-implantation blastocysts are estrogenic.
我们研究了猪体内细胞色素P450芳香化酶组织(卵巢、子宫内膜/胎盘和着床前胚泡)同工型合成的染色体基础。克隆并鉴定了源自三个不同猪芳香化酶染色体基因的DNA片段。发现编码胚泡芳香化酶同工型的猪III型芳香化酶基因由九个编码外显子和两个相互排斥的5'非翻译外显子(命名为E1A和E1B)组成,总共跨越30 kb或更长。通过克隆跨越相应外显子7、8和9的基因组DNA片段,鉴定出编码子宫内膜/胎盘芳香化酶同工型的猪II型芳香化酶基因。另外两个噬菌体克隆的DNA插入片段包含编码卵巢芳香化酶同工型的第三个染色体基因(I型)的外显子2、3和4。发现这些基因组片段中的所有内含子-外显子连接在相对位置上与单拷贝人类芳香化酶基因的相同。cDNA和基因组序列的比较表明,这些基因相应外显子上的核苷酸序列变异并不均匀,而相应的内含子序列是保守的。II型和III型芳香化酶基因定位于猪1号染色体上的同一区域位置(q16 - 17),该区域与人类芳香化酶基因所在的人类15号染色体区域(q21.1)同源。结果表明,本研究中鉴定的三个芳香化酶基因在整体结构组织上似乎相似,很可能是成簇的,这可能是由至少两个独立的基因复制事件导致的。多个芳香化酶基因的存在构成了一种新描述的机制,通过该机制可以以组织和时间方式调节芳香化酶的生物合成和功能活性,并进一步凸显了哺乳动物中芳香化酶基因表达的复杂性。此外,在猪胚泡中高度表达的独特芳香化酶基因的存在可能为其他哺乳动物(如马科动物、兔子、仓鼠)提供一个范例,这些动物的着床前胚泡具有雌激素活性。