Research Resource: Whole Transcriptome RNA Sequencing Detects Multiple 1α,25-Dihydroxyvitamin D3-Sensitive Metabolic Pathways in Developing Zebrafish

Author:

Craig Theodore A.1,Zhang Yuji2,McNulty Melissa S.1,Middha Sumit2,Ketha Hemamalini1,Singh Ravinder J.3,Magis Andrew T.4,Funk Cory5,Price Nathan D.5,Ekker Stephen C.6,Kumar Rajiv16

Affiliation:

1. Nephrology and Hypertension Research (T.A.C., M.S.M., H.K., R.K.), Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905;

2. Division of Biomedical Statistics and Informatics (Y.Z., S.M.), Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota 55905;

3. Department of Laboratory Medicine and Pathology (R.J.S.), Mayo Clinic, Rochester, Minnesota 55905;

4. Center for Biophysics and Computational Biology (A.T.M.), University of Illinois, Urbana-Champaign, Urbana, Illinois 61801;

5. Institute for Systems Biology (C.F., N.D.P.), Seattle, Washington 98109-5234

6. Department of Biochemistry and Molecular Biology (S.C.E., R.K.), Mayo Clinic, Rochester, Minnesota 55905;

Abstract

AbstractThe biological role of vitamin D receptors (VDR), which are abundantly expressed in developing zebrafish (Danio rerio) as early as 48 h after fertilization, and before the development of a mineralized skeleton and mature intestine and kidney, is unknown. We probed the role of VDR in developing zebrafish biology by examining changes in expression of RNA by whole transcriptome shotgun sequencing (RNA-seq) in fish treated with picomolar concentrations of the VDR ligand and hormonal form of vitamin D3, 1α,25-dihydroxyvitamin D3 [1α,25(OH)2D3)].We observed significant changes in RNAs of transcription factors, leptin, peptide hormones, and RNAs encoding proteins of fatty acid, amino acid, xenobiotic metabolism, receptor-activator of NFκB ligand (RANKL), and calcitonin-like ligand receptor pathways. Early highly restricted, and subsequent massive changes in more than 10% of expressed cellular RNA were observed. At days post fertilization (dpf) 2 [24 h 1α,25(OH)2D3-treatment], only four RNAs were differentially expressed (hormone vs. vehicle). On dpf 4 (72 h treatment), 77 RNAs; on dpf 6 (120 h treatment) 1039 RNAs; and on dpf 7 (144 h treatment), 2407 RNAs were differentially expressed in response to 1α,25(OH)2D3. Fewer RNAs (n = 481) were altered in dpf 7 larvae treated for 24 h with 1α,25(OH)2D3vs. those treated with hormone for 144 h. At dpf 7, in 1α,25(OH)2D3-treated larvae, pharyngeal cartilage was larger and mineralization was greater. Changes in expression of RNAs for transcription factors, peptide hormones, and RNAs encoding proteins integral to fatty acid, amino acid, leptin, calcitonin-like ligand receptor, RANKL, and xenobiotic metabolism pathways, demonstrate heretofore unrecognized mechanisms by which 1α,25(OH)2D3 functions in vivo in developing eukaryotes.

Publisher

The Endocrine Society

Subject

Endocrinology,Molecular Biology,General Medicine

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