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LIM 同源框蛋白 mLIM3/Lhx3 通过一条不依赖 Pit-1/GHF-1 的途径诱导促肾上腺皮质激素瘤 AtT20 细胞中催乳素基因的表达。

The LIM homeobox protein mLIM3/Lhx3 induces expression of the prolactin gene by a Pit-1/GHF-1-independent pathway in corticotroph AtT20 cells.

作者信息

Girardin S E, Benjannet S, Barale J C, Chrétien M, Seidah N G

机构信息

Laboratory of Biochemical Neuroendocrinology, Clinical Research Institute of Montreal, Qué., Canada.

出版信息

FEBS Lett. 1998 Jul 24;431(3):333-8. doi: 10.1016/s0014-5793(98)00787-x.

Abstract

mLIM3, a member of the LIM homeobox family, was recently demonstrated to be critical for proliferation and differentiation of the pituitary cell lineage. Using a pool of degenerate oligonucleotides we determined the DNA sequence ANNAGGAAA(T/C)GA(CIG)AA as the set preferentially recognized by mLIM3. A nearly identical sequence is found in the prolactin (PRL) promoter, within a 15-mer stretch from nucleotides (nts) -218 to -204 which is highly conserved between human, rat, and bovine. In order to test the hypothesis of a transcriptional effect of mLIM3 on the prolactin promoter, stable transfectants of mLIM3 cDNA in AtT20 tumor cells revealed that PRL mRNA expression was induced in 3 separate stable clones. Gel retardation experiments performed using nuclear extracts isolated from one of the AtT20/mLIM3 stable transfectants revealed affinity towards the 15-mer element of the PRL promoter. From these results, we propose that the PRL promoter element (nts -218 to -204) could be functional in vivo. Finally, we demonstrate that in AtT20 cells prolactin mRNA expression is not induced by the Pit-1/GHF-1 pathway and that growth hormone mRNA is not detected concomitantly with prolactin. We conclude that mLIM3 may play a key role in inducing PRL gene expression in lactotrophs by binding to a conserved motif close to a Pit-1/GHF-1 site within the proximal PRL promoter.

摘要

mLIM3是LIM同源框家族的成员之一,最近的研究表明它对垂体细胞谱系的增殖和分化至关重要。我们使用一组简并寡核苷酸确定了DNA序列ANNAGGAAA(T/C)GA(CIG)AA为mLIM3优先识别的序列。在催乳素(PRL)启动子中发现了一个几乎相同的序列,位于从核苷酸(nts)-218至-204的15聚体片段内,该片段在人、大鼠和牛之间高度保守。为了验证mLIM3对催乳素启动子具有转录作用的假设,AtT20肿瘤细胞中mLIM3 cDNA的稳定转染子显示,在3个独立的稳定克隆中PRL mRNA表达被诱导。使用从其中一个AtT20/mLIM3稳定转染子中分离的核提取物进行的凝胶阻滞实验表明,其对PRL启动子的15聚体元件具有亲和力。基于这些结果,我们提出PRL启动子元件(nts -218至-204)在体内可能具有功能。最后,我们证明在AtT20细胞中,催乳素mRNA表达不是由Pit-1/GHF-1途径诱导的,并且生长激素mRNA与催乳素不会同时被检测到。我们得出结论,mLIM3可能通过与近端PRL启动子内靠近Pit-1/GHF-1位点的保守基序结合,在诱导泌乳细胞中PRL基因表达方面发挥关键作用。

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