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一种长链非编码RNA,作为直接的维生素D靶标,由人类HSD17B2基因座的反义链转录而来。

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

作者信息

Kanemoto Yoshiaki, Nishimura Koichi, Hayakawa Akira, Sawada Takahiro, Amano Rei, Mori Jinichi, Kurokawa Tomohiro, Murakami Yoshinori, Kato Shigeaki

机构信息

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

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

出版信息

Biosci Rep. 2022 May 27;42(5). doi: 10.1042/BSR20220321.

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.

摘要

在生理和病理条件下,维生素D(VD)通过由核维生素D受体(VDR)介导的基因调控发挥多种作用。然而,已知的VDR靶基因似乎无法解释所有的VD作用。我们利用人细胞系中的计算机和转录组学方法,直接寻找受VD转录调控的非编码RNA。我们发现了4种长链非编码RNA(lncRNA),但未发现微小RNA(miRNA),编码区存在一致的VDR结合基序支持了这一结果。其中一种lncRNA(AS-HSD17β2)从HSD17β2基因座的反义链转录而来,HSD17β2基因座也是VD的直接靶点。AS-HSD17β2减弱了HSD17β2的表达。因此,AS-HSD17β2代表了VD的一个直接lncRNA靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e7a/9142830/65c5111d2442/bsr-42-bsr20220321-g1.jpg

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