Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

Genomic alterations in primary hyperaldosteronism

ABSTRACT: Transcriptome comparison of an aldosterone producing adenoma transcriptome and its adjacent zona glomerulosa. Both tissues are from the same individual, are differentiated for aldosterone production, but the adjacent zona glomerulosa produces no aldosterone by negative feedback. Keywords = aldosterone producing adenoma transcriptome Keywords: parallel sample

ORGANISM(S): Homo sapiens

SUBMITTER: Guillaume Assié

PROVIDER: E-GEOD-2017 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Steroidogenesis in aldosterone-producing adenoma revisited by transcriptome analysis.

Assié Guillaume G Auzan Colette C Gasc Jean-Marie JM Baviera Erno E Balaton André A Elalouf Jean-Marc JM Jeunemaitre Xavier X Plouin Pierre-François PF Corvol Pierre P Clauser Eric E

The Journal of clinical endocrinology and metabolism 20051004 12

<h4>Context</h4>Primary aldosteronism (PAL) is the most frequent cause of secondary arterial hypertension. In PAL, aldosterone production is chronic, excessive, and autonomous.<h4>Objective</h4>The objective of this study was to identify the angiotensin-II independent alterations of steroidogenesis responsible for PAL.<h4>Design</h4>Genomewide gene expression was compared in two tissues differentiated for aldosterone production, both nonstimulated by circulating angiotensin II and differing in t ...[more]

PMID: 16204365

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Project description:In order to analyze the transcriptome characteristics of aldosterone producing cell clusters (APCC) we compared transcript abundances of APCC, zona glomerulosa (ZG), zona fasciculata (ZF), and zona reticularis (ZR), from adrenal glands obtained from 4 kidney transplantation donors. The frozen adrenal glands in O.C.T. compound were cut into 7um sections, and every 10-th section immunostained for aldosterone synthase (CYP11B2). The remaining sections were stained with cresyl violet and used for laser-capture microdissection of tissue to use in the array assays. APCC and ZG samples were captured from CYP11B2 positive regions based on the CYP11B2-stained sections. ZF and ZR were captured from lipid-rich cells in the middle layer and compact cells outside of the medulla, respectively. RNA was isolated using PicoPure RNA isolation kits (Molecular Devices, Sunnyvale, CA). 1-10 ng total RNA was reverse-transcribed and amplified with the Ovation Pico WTA System V2 (NuGEN Technologies, San Carlos, CA). cDNA was purified using QIAquick PCR Purification Kit (Qiagen, Hilden, Germany) and biotin-labeled using Encore Biotin Module (NuGEN Technologies), followed by hybridization to GeneChip Human Genome U133 Plus 2.0 Array (Affymetrix, Santa Clara, CA). Expression values were calculated using the robust multi-array average method (RMA). This resulted in base-2 log-transformed data for each of the 4 tissues from each of the 4 people. In addition to the raw and processed data we also supply a supplementary Excel file holding the data and some statistical analysis, which has features to make simple graphs, and holds probe-set annotation that we used at that time (users may wish to obtain new annotation though). We fit two-way ANOVA models with terms for 4 tissues and 4 people, and compared each probe-set between every pair of tissues using F-tests for pairwise contrasts. We modeled people effects since they were not negligible. The supplement shows how to calculate the tests. Aldosterone producing cell clusters (APCC), zona glomerulosa (ZG), zona fasciculata (ZF), and zona reticularis (ZR), from adrenal glands obtained from 4 kidney transplantation donors, were individually assayed on 16 Affymetrix GeneChip Human Genome U133 Plus 2.0 Arrays. Expression values were estimated with the Robust Multi-Arry average (RMA) algorithm, which resulted in log-2 transformed values for each of 54675 probe sets.

Dataset Information

Genomic alterations in primary hyperaldosteronism

Publications

Steroidogenesis in aldosterone-producing adenoma revisited by transcriptome analysis.

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