Developmental Programming: Adipose Depot-Specific Regulation of Non-Coding RNAs and Their Relation to Coding RNA Expression in Prenatal Testosterone and Prenatal Bisphenol-a -Treated Female Sheep
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2023/03/15
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Description:Inappropriate developmental exposure to steroids is linked to metabolic disorders. Prenatal testosterone excess or bisphenol A (BPA, an environmental estrogen mimic) leads to insulin resistance and adipocyte disruptions in female lambs. Adipocytes are key regulators of insulin sensitivity. Metabolic tissue-specific differences in insulin sensitivity coupled with adipose depot-specific changes in key mRNAs, were previously observed with prenatal steroid exposure. We hypothesized that depot-specific changes in the non-coding RNA (ncRNA) - regulators of gene expression would account for the direction of changes seen in mRNAs. Non-coding RNA (lncRNA, miRNA, snoRNA, snRNA) from various adipose depots of prenatal testosterone and BPA-treated animals were sequenced. Adipose depot-specific changes in the ncRNA that are consistent with the depot-specific mRNA expression in terms of directionality of changes and functional implications in insulin resistance, adipocyte differentiation and cardiac hypertrophy were found. Importantly, the adipose depot-specific ncRNA changes were model-specific and mutually exclusive, suggestive of different regulatory entry points in this regulation. [Description provided by NIOSH]
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ISSN:0303-7207
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Volume:564
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NIOSHTIC Number:nn:20070615
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Citation:Mol Cell Endocrinol 2023 Mar; 564:111868
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Contact Point Address:Kelly Bakulski, Department of Epidemiology, M5511 SPH II, Ann Arbor, MI, 48109, USA
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Email:bakulski@umich.edu
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Federal Fiscal Year:2023
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Performing Organization:University of Michigan, Ann Arbor
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Peer Reviewed:True
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Start Date:20050701
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Source Full Name:Molecular and Cellular Endocrinology
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End Date:20280630
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Main Document Checksum:urn:sha-512:eeca925490c6f703f1aa0e8330aea916dc6fa03c4cf80d3942a11679a88e0761a33001876edec8923ffd5eae7eb8e232ac0b2b23f517b0babee340739e088148
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