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Mol. Cells 2012; 33(2): 111-116

Published online January 2, 2012

https://doi.org/10.1007/s10059-012-2164-x

© The Korean Society for Molecular and Cellular Biology

Identification and Characterization of a Non-coding RNA at the Mouse Pcna Locus

Ji-Yeon Lee1,4, Abdul Aziz Khan1,3,4, Hyehyun Min1,2, Xinnan Wang1, and Myoung Hee Kim1,2,*

1Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine, Seoul 120-752, Korea, 2Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Korea, 3Present address: Department of Life Science, Pohang University of Science and Technology, Pohang 790-784, Korea, 4These authors contributed equally to this work.

Correspondence to : *Correspondence: mhkim1@yuhs.ac

Received: August 9, 2011; Revised: November 15, 2011; Accepted: November 29, 2011

Abstract

AK007836 encodes a noncoding RNA (ncRNA) consist-ing of 2 exons. Since AK007836 is located just upstream of Pcna and transcribed in the opposite direction to that of Pcna, we analyzed its expression pattern. Both ncRNA and Pcna expressions were detected in in vitro and in vivo cells, showing a positive correlation. A 177 bp region se-parating the first exons of Pcna and AK007836 has a bidirectional promoter activity. When the expression of ncRNA was reduced by siRNA, Pcna expression was also reduced in normal cells, but not in cancer cells. These results suggest that the ncRNA is divergently transcribed from the bidirectional promoter, positively regulating the neighboring protein-coding Pcna gene transcription, and this regulatory function is somehow disrupted in cancer cells.

Keywords bidirectional promoter, co-expression, gene regulation, non-coding RNA, Pcna

Article

Research Article

Mol. Cells 2012; 33(2): 111-116

Published online February 29, 2012 https://doi.org/10.1007/s10059-012-2164-x

Copyright © The Korean Society for Molecular and Cellular Biology.

Identification and Characterization of a Non-coding RNA at the Mouse Pcna Locus

Ji-Yeon Lee1,4, Abdul Aziz Khan1,3,4, Hyehyun Min1,2, Xinnan Wang1, and Myoung Hee Kim1,2,*

1Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine, Seoul 120-752, Korea, 2Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Korea, 3Present address: Department of Life Science, Pohang University of Science and Technology, Pohang 790-784, Korea, 4These authors contributed equally to this work.

Correspondence to:*Correspondence: mhkim1@yuhs.ac

Received: August 9, 2011; Revised: November 15, 2011; Accepted: November 29, 2011

Abstract

AK007836 encodes a noncoding RNA (ncRNA) consist-ing of 2 exons. Since AK007836 is located just upstream of Pcna and transcribed in the opposite direction to that of Pcna, we analyzed its expression pattern. Both ncRNA and Pcna expressions were detected in in vitro and in vivo cells, showing a positive correlation. A 177 bp region se-parating the first exons of Pcna and AK007836 has a bidirectional promoter activity. When the expression of ncRNA was reduced by siRNA, Pcna expression was also reduced in normal cells, but not in cancer cells. These results suggest that the ncRNA is divergently transcribed from the bidirectional promoter, positively regulating the neighboring protein-coding Pcna gene transcription, and this regulatory function is somehow disrupted in cancer cells.

Keywords: bidirectional promoter, co-expression, gene regulation, non-coding RNA, Pcna

Mol. Cells
Dec 31, 2023 Vol.46 No.12, pp. 727~777
COVER PICTURE
Lee et al. (pp. 757-763), show that disruption of ANKS1A promotes the entry of intraflagellar transport trains into cilia, increasing protein transport and forming extracellular vesicles (ECVs). This figure illustrates the abundance of ECVs along the cilia of primary ependymal cells derived from ANKS1A KO mice.

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