A long non-coding RNA as a direct vitamin D target transcribed from the antisense strand of the human HSD17B2 locus

Author:

Kanemoto Yoshiaki123,Nishimura Koichi12,Hayakawa Akira12,Sawada Takahiro12,Amano Rei12,Mori Jinichi1245,Kurokawa Tomohiro124,Murakami Yoshinori3,Kato Shigeaki124ORCID

Affiliation:

1. 1Department of Medical Epigenetics, Research Institute of Innovative Medicine, Tokiwa Foundation, Iwaki, Fukushima, Japan

2. 2Department of Medical Genome Research, Graduate School of Life Science and Engineering, Iryo Sosei University, Iino, Chuo-dai, Iwaki, Fukushima 9708551, Japan

3. 3Division of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan

4. 4Department of Basic Pathology, School of Medicine, Fukushima Medical University, Fukushima, Fukushima 960-1295, Japan

5. 5Department of Hematology, Jyoban Hospital, Tokiwa Foundation, Iwaki, Fukushima, Japan

Abstract

Abstract Vitamin D (VD) exerts a wide variety of actions via gene regulation mediated by the nuclear vitamin D receptor (VDR) under physiological and pathological settings. However, the known target genes of VDR appear unlikely to account for all VD actions. We used in silico and transcriptomic approaches in human cell lines to search for non-coding RNAs transcriptionally regulated by VD directly. Four long non-coding RNAs (lncRNAs), but no microRNAs (miRNAs), were found, supported by the presence of consensus VDR-binding motifs in the coding regions. One of these lncRNAs (AS-HSD17β2) is transcribed from the antisense strand of the HSD17β2 locus, which is also a direct VD target. AS-HSD17β2 attenuated HSD17β2 expression. Thus, AS-HSD17β2 represents a direct lncRNA target of VD.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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