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Pituitary homeobox 2 regulates adrenal4 binding protein/steroidogenic factor-1 gene transcription in the pituitary gonadotrope through interaction with the intronic enhancer.垂体同源盒蛋白2通过与内含子增强子相互作用调节垂体促性腺细胞中肾上腺4结合蛋白/类固醇生成因子-1基因的转录。
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Adrenal development is initiated by Cited2 and Wt1 through modulation of Sf-1 dosage.肾上腺发育由Cited2和Wt1通过调节Sf-1剂量启动。
Development. 2007 Jun;134(12):2349-58. doi: 10.1242/dev.004390.
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Adrenocortical cells with stem/progenitor cell properties: recent advances.具有干细胞/祖细胞特性的肾上腺皮质细胞:最新进展
Mol Cell Endocrinol. 2007 Feb;265-266:10-6. doi: 10.1016/j.mce.2006.12.028. Epub 2007 Jan 19.
4
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function.类固醇生成因子1(SF1/Ad4BP,NR5A1)的杂合错义突变与肾上腺功能正常的46,XY性发育障碍相关。
J Clin Endocrinol Metab. 2007 Mar;92(3):991-9. doi: 10.1210/jc.2006-1672. Epub 2007 Jan 2.
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Identification of a novel population of adrenal-like cells in the mammalian testis.在哺乳动物睾丸中鉴定出一种新型的肾上腺样细胞群体。
Dev Biol. 2006 Nov 1;299(1):250-6. doi: 10.1016/j.ydbio.2006.07.030. Epub 2006 Jul 31.
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Expression and spatio-temporal distribution of differentiation and proliferation markers during mouse adrenal development.小鼠肾上腺发育过程中分化和增殖标志物的表达及时空分布
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Two-step regulation of Ad4BP/SF-1 gene transcription during fetal adrenal development: initiation by a Hox-Pbx1-Prep1 complex and maintenance via autoregulation by Ad4BP/SF-1.胎儿肾上腺发育过程中Ad4BP/SF-1基因转录的两步调节:由Hox-Pbx1-Prep1复合体启动并通过Ad4BP/SF-1自身调节维持。
Mol Cell Biol. 2006 Jun;26(11):4111-21. doi: 10.1128/MCB.00222-06.
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Ventromedial hypothalamic nucleus-specific enhancer of Ad4BP/SF-1 gene.Ad4BP/SF-1基因的腹内侧下丘脑核特异性增强子。
Mol Endocrinol. 2005 Nov;19(11):2812-23. doi: 10.1210/me.2004-0431. Epub 2005 Jun 30.
9
Mouse Polycomb M33 is required for splenic vascular and adrenal gland formation through regulating Ad4BP/SF1 expression.小鼠多梳蛋白M33通过调节Ad4BP/SF1的表达,对脾脏血管和肾上腺的形成是必需的。
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Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones.从胆固醇到活性甾体激素途径中的甾体生成酶概述。
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通过谱系追踪揭示肾上腺皮质胎儿区与成人区之间的发育联系。

Developmental links between the fetal and adult zones of the adrenal cortex revealed by lineage tracing.

作者信息

Zubair Mohamad, Parker Keith L, Morohashi Ken-ichirou

机构信息

Division of Sex Differentiation, National Institute for Basic Biology, National Institutes of Natural Sciences,Okazaki, Japan.

出版信息

Mol Cell Biol. 2008 Dec;28(23):7030-40. doi: 10.1128/MCB.00900-08. Epub 2008 Sep 22.

DOI:10.1128/MCB.00900-08
PMID:18809574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2593385/
Abstract

The nuclear receptor Ad4BP/SF-1 is essential for development of the adrenal cortex and the gonads, which derive from a common adrenogonadal primordium. The adrenal cortex subsequently forms morphologically distinct compartments: the inner (fetal) and outer (definitive or adult) zones. Despite considerable effort, the mechanisms that mediate the differential development of the adrenal and gonadal primordia and the fetal and adult adrenal cortices remain incompletely understood. We previously identified a fetal adrenal-specific enhancer (FAdE) in the Ad4BP/SF-1 locus that directs transgene expression to the fetal adrenal cortex and demonstrated that this enhancer is autoregulated by Ad4BP/SF-1. We now combine the FAdE with the Cre/loxP system to trace cell lineages in which the FAdE was active at some stage in development. These lineage-tracing studies establish definitively that the adult cortex derives from precursor cells in the fetal cortex in which the FAdE was activated before the organization into two distinct zones. The potential of these fetal adrenocortical cells to enter the pathway that eventuates in cells of the adult cortex disappeared by embryonic day 14.5. Thus, these studies demonstrate a direct link between the fetal and adult cortices involving a transition that must occur before a specific stage of development.

摘要

核受体Ad4BP/SF-1对于肾上腺皮质和性腺的发育至关重要,而肾上腺皮质和性腺起源于共同的肾上腺生殖嵴原基。肾上腺皮质随后形成形态上不同的部分:内层(胎儿期)和外层(终末或成年期)区域。尽管付出了巨大努力,但介导肾上腺和性腺原基以及胎儿和成年肾上腺皮质差异发育的机制仍未完全了解。我们之前在Ad4BP/SF-1基因座中鉴定出一个胎儿肾上腺特异性增强子(FAdE),它将转基因表达导向胎儿肾上腺皮质,并证明该增强子受Ad4BP/SF-1自身调节。我们现在将FAdE与Cre/loxP系统结合起来,追踪在发育的某个阶段FAdE活跃的细胞谱系。这些谱系追踪研究明确证实,成年皮质起源于胎儿皮质中的前体细胞,在这些细胞组织成两个不同区域之前FAdE就已被激活。这些胎儿肾上腺皮质细胞进入最终形成成年皮质细胞途径的潜能在胚胎第14.5天时消失。因此,这些研究证明了胎儿和成年皮质之间存在直接联系,涉及一个必须在特定发育阶段之前发生的转变。