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鉴定出两个新的促肾上腺皮质激素(ACTH)反应性基因,它们分别编码锰依赖性超氧化物歧化酶(SOD2)和锌指蛋白TIS11b [十四烷酰佛波醇乙酸酯(TPA)诱导序列11b]。

Identification of two novel ACTH-responsive genes encoding manganese-dependent superoxide dismutase (SOD2) and the zinc finger protein TIS11b [tetradecanoyl phorbol acetate (TPA)-inducible sequence 11b].

作者信息

Chinn Anna M, Ciais Delphine, Bailly Sabine, Chambaz Edmond, LaMarre Jonathan, Feige Jean-Jacques

机构信息

INSERM EMI 01-05, Department of Molecular and Structural Biology, Commissariat à l'Energie Atomique, Grenoble, France F-38054.

出版信息

Mol Endocrinol. 2002 Jun;16(6):1417-27. doi: 10.1210/mend.16.6.0844.

Abstract

ACTH is the major trophic factor regulating and maintaining adrenocortical function, affecting such diverse processes as steroidogenesis, cell proliferation, cell migration, and cell survival. We used differential display RT-PCR to identify genes that are rapidly induced by ACTH in the bovine adrenal cortex. Of 42 PCR products differentially amplified from primary cultures of bovine adrenocortical cells treated with 10 nM ACTH, six identified mRNAs that were confirmed by Northern blot analysis to be induced by ACTH. Four of these amplicons encoded noninformative repetitive sequences. Of the other two sequenced amplicons, one encoded a partial sequence for mitochondrial manganese-dependent superoxide dismutase (SOD2), an enzyme that is likely to protect adrenocortical cells from the cytotoxic effects of radical oxygen species generated during steroid biosynthesis. The second was identified as TIS11b (phorbol-12-myristate-13-acetate-inducible sequence 11b)/ERF-1/cMG, a member of the CCCH double-zinc finger protein family. SOD2 induction by ACTH was independent of extracellular steroid concentration or oxidative stress. SOD2 and TIS11b mRNA expressions were rapidly induced by ACTH, reaching a maximal level after 8 h and 3 h of treatment, respectively. These ACTH effects were mimicked by forskolin but appeared independent of cortisol secretion. Upon ACTH treatment, induction of TIS11b expression closely followed the previously characterized peak of vascular endothelial growth factor (VEGF) expression. Transfection of a TIS11b expression plasmid into 3T3 fibroblasts induced a decrease in the expression of a reporter gene placed upstream of the VEGF 3'-untranslated region, indicating that TIS11b may be an important regulator of VEGF expression through interaction with its 3'-untranslated region.

摘要

促肾上腺皮质激素(ACTH)是调节和维持肾上腺皮质功能的主要营养因子,影响着诸如类固醇生成、细胞增殖、细胞迁移和细胞存活等多种不同的过程。我们使用差异显示逆转录聚合酶链反应(RT-PCR)来鉴定在牛肾上腺皮质中被ACTH快速诱导的基因。在用10 nM ACTH处理的牛肾上腺皮质细胞原代培养物中差异扩增得到的42个PCR产物中,有6个鉴定出的mRNA经Northern印迹分析证实是由ACTH诱导的。这些扩增子中有4个编码无信息的重复序列。在另外两个测序的扩增子中,一个编码线粒体锰依赖性超氧化物歧化酶(SOD2)的部分序列,该酶可能保护肾上腺皮质细胞免受类固醇生物合成过程中产生的活性氧的细胞毒性作用。另一个被鉴定为TIS11b(佛波醇-12-肉豆蔻酸酯-13-乙酸酯诱导序列11b)/ERF-1/cMG,它是CCCH双锌指蛋白家族的成员。ACTH对SOD2的诱导独立于细胞外类固醇浓度或氧化应激。ACTH可快速诱导SOD2和TIS11b mRNA表达,分别在处理8小时和3小时后达到最高水平。这些ACTH的作用可被福斯可林模拟,但似乎与皮质醇分泌无关。在ACTH处理后,TIS11b表达的诱导紧跟先前表征的血管内皮生长因子(VEGF)表达峰值。将TIS11b表达质粒转染到3T3成纤维细胞中会导致位于VEGF 3'-非翻译区上游的报告基因表达下降,表明TIS11b可能通过与其3'-非翻译区相互作用而成为VEGF表达的重要调节因子。

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