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垂体功能减退症的分子基础。

The molecular basis of hypopituitarism.

作者信息

Radovick S, Cohen L E, Wondisford F E

机构信息

Department of Medicine, Harvard Medical School, Boston, Mass, USA.

出版信息

Horm Res. 1998;49 Suppl 1:30-6. doi: 10.1159/000053065.

Abstract

Pit-1 is a pituitary-specific transcription factor responsible for pituitary development and hormone expression in mammals. My laboratory and others have recently described several patients with combined pituitary hormone deficiency (CPHD) due to point mutations in the pit-1 gene. In addition to pit-1, other nuclear factors appear to be necessary for full expression of pituitary genes. A zinc finger transcription factor, Zn-15, is responsible with pit-1 for synergistic activation of the GH gene. The Pr1 gene is regulated synergistically by pit-1 and the estrogen receptor. Finally, the pit-1 gene itself is regulated by an enhancer element located > 10 kb upstream of the transcriptional start. This element contains several pit-1 DNA binding sites and retinoic acid response elements (RAREs). On one of these elements, pit-1 and RAR interact functionally to mediate a synergistic response to RA. Recent data from our laboratory suggests that RA induction of the pit-1 gene can be impaired by pit-1 gene mutations. Study of pit-1 mutations and their diverse pathophysiological mechanisms should increase our understanding of anterior pituitary gland development and gene regulation in normal and disease states.

摘要

Pit-1是一种垂体特异性转录因子,负责哺乳动物垂体的发育和激素表达。我的实验室和其他机构最近描述了几位因pit-1基因突变而患有联合垂体激素缺乏症(CPHD)的患者。除了pit-1之外,其他核因子似乎对于垂体基因的完全表达也是必需的。一种锌指转录因子Zn-15与pit-1共同负责生长激素(GH)基因的协同激活。Pr1基因受pit-1和雌激素受体的协同调控。最后,pit-1基因本身受位于转录起始点上游超过10 kb处的一个增强子元件调控。该元件包含几个pit-1 DNA结合位点和视黄酸反应元件(RAREs)。在其中一个元件上,pit-1和视黄酸受体(RAR)在功能上相互作用,介导对视黄酸(RA)的协同反应。我们实验室最近的数据表明,pit-1基因突变可能会损害RA对pit-1基因的诱导作用。对pit-1突变及其多样的病理生理机制的研究,应该会增进我们对正常和疾病状态下垂体前叶发育及基因调控的理解。

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