Ponglikitmongkol M, Green S, Chambon P
Laboratoire de Génétique Moléculaire, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, France.
EMBO J. 1988 Nov;7(11):3385-8. doi: 10.1002/j.1460-2075.1988.tb03211.x.
The oestrogen receptor (ER) is a ligand-activated transcription factor composed of several domains important for hormone binding, DNA binding and activation of transcription. We show here that the human ER gene is greater than 140 kb in length, split into eight exons and that the positions of these introns have been highly conserved when compared with the chicken progesterone receptor and are remarkably similar to those of one of the chicken thyroid hormone receptor genes. The N-terminal A/B region, which is not conserved between the different members of the nuclear receptor family, is almost entirely encoded within a single exon. Notably each of the putative 'zinc fingers' of the receptor DNA-binding domain is encoded separately, and the hormone-binding domain is assembled from five exons. In addition, we find that the ER isolated from the human breast cancer cell line MCF-7 contains a Gly-400----Val mutation present in the hormone-binding domain.
雌激素受体(ER)是一种配体激活的转录因子,由对激素结合、DNA结合和转录激活重要的几个结构域组成。我们在此表明,人类ER基因长度超过140 kb,分为八个外显子,与鸡孕激素受体相比,这些内含子的位置高度保守,并且与鸡甲状腺激素受体基因之一的内含子位置非常相似。核受体家族不同成员之间不保守的N端A/B区域几乎完全由单个外显子编码。值得注意的是,受体DNA结合结构域的每个假定“锌指”都是单独编码的,激素结合结构域由五个外显子组装而成。此外,我们发现从人乳腺癌细胞系MCF-7分离出的ER在激素结合结构域中存在Gly-400→Val突变。