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超日周期糖皮质激素暴露在体内指导基因依赖性和组织特异性mRNA表达模式。

Ultradian glucocorticoid exposure directs gene-dependent and tissue-specific mRNA expression patterns in vivo.

作者信息

George Charlotte L, Birnie Matthew T, Flynn Benjamin P, Kershaw Yvonne M, Lightman Stafford L, Conway-Campbell Becky L

机构信息

Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, School of Clinical Sciences, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol, BS1 3NY, UK; CGAT, MRC Weatherall Institute of Molecular Medicine Centre for Computational Biology, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9DS, UK.

Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, School of Clinical Sciences, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol, BS1 3NY, UK.

出版信息

Mol Cell Endocrinol. 2017 Jan 5;439:46-53. doi: 10.1016/j.mce.2016.10.019. Epub 2016 Oct 18.

Abstract

In this paper we report differential decoding of the ultradian corticosterone signal by glucocorticoid target tissues. Pulsatile corticosterone replacement in adrenalectomised rats resulted in different dynamics of Sgk1 mRNA production, with a distinct pulsatile mRNA induction profile observed in the pituitary in contrast to a non-pulsatile induction in the prefrontal cortex (PFC). We further report the first evidence for pulsatile transcriptional repression of a glucocorticoid-target gene in vivo, with pulsatile regulation of Pomc transcription in pituitary. We have explored a potential mechanism for differences in the induction dynamics of the same transcript (Sgk1) between the PFC and pituitary. Glucocorticoid receptor (GR) activation profiles were strikingly different in pituitary and prefrontal cortex, with a significantly greater dynamic range and shorter duration of GR activity detected in the pituitary, consistent with the more pronounced gene pulsing effect observed. In the prefrontal cortex, expression of Gilz mRNA was also non-pulsatile and exhibited a significantly delayed timecourse of increase and decrease when compared to Sgk1, additionally highlighting gene-specific regulatory dynamics during ultradian glucocorticoid treatment.

摘要

在本文中,我们报告了糖皮质激素靶组织对超日周期皮质酮信号的差异解码。对肾上腺切除的大鼠进行脉冲式皮质酮替代治疗,导致Sgk1 mRNA产生的动态变化不同,垂体中观察到明显的脉冲式mRNA诱导模式,而前额叶皮质(PFC)中则是非脉冲式诱导。我们还首次报告了体内糖皮质激素靶基因的脉冲式转录抑制的证据,即垂体中Pomc转录的脉冲式调节。我们探讨了PFC和垂体中同一转录本(Sgk1)诱导动态差异的潜在机制。糖皮质激素受体(GR)的激活模式在垂体和前额叶皮质中显著不同,垂体中检测到的GR活性动态范围明显更大且持续时间更短,这与观察到的更明显的基因脉冲效应一致。在前额叶皮质中,Gilz mRNA的表达也是非脉冲式的,与Sgk1相比,其增减的时间进程明显延迟,这进一步突出了超日周期糖皮质激素治疗期间基因特异性的调控动态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37eb/5131830/6d6cf0716d8f/gr1.jpg

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