TOP

Research Article

Split Viewer

Mol. Cells 2013; 35(4): 285-290

Published online March 18, 2013

https://doi.org/10.1007/s10059-013-2275-z

© The Korean Society for Molecular and Cellular Biology

Expression and Imprinting Analysis of AK044800, a Transcript from the Dlk1-Dio3 Imprinted Gene Cluster during Mouse Embryogenesis

Zhengbin Han, Qi Liu, Zhijun Huang, Wei Cui, Yijun Tian, Weili Yan, and Qiong Wu

School of Life Science and Technology, Harbin Institute of Technology, Science Park of Harbin Institute of Technology, Harbin, China

Received: October 19, 2013; Revised: January 25, 2013; Accepted: February 4, 2013

Abstract

Recent advances of induced pluripotent stem cells (iPSCs) has demonstrated that full development potential is closely related with the expression state of noncoding RNAs (ncRNAs) of the Dlk1-Dio3 imprinted gene cluster. However, few of them, especially the long noncoding RNAs (lncRNAs), have been characterized in detail. AK044800 is a transcript from the Dlk1-Dio3 imprinted region with little known information. This study reports original data on the expression pattern of AK044800 during embryogenesis. Expression analysis showed that AK044800 was specifically expressed in the brain at mid-gestation, E9.5 and E11.5. And at E15.5, its expression was mainly concentrated in the forebrain. In the late-gestation stage (E18.5), AK044800 expression was weaker in the brain and began to emerge in some other tissues during this period. Notably, the expression of AK044800 was biallelic in the brain, unlike other noncoding transcripts from this imprinted region. In addition, its expression was dependent on inbred mouse strains. This may be the first lncRNA that has been identified with a different expression between inbred mouse strains. This study may provide useful clues for
further investigations of expression regulation and functions of lncRNAs of the Dlk1-Dio3 imprinted region.

Keywords AK044800, expression patterns, imprinting analysis, inbred mouse strains, long noncoding RNAs

Article

Research Article

Mol. Cells 2013; 35(4): 285-290

Published online April 30, 2013 https://doi.org/10.1007/s10059-013-2275-z

Copyright © The Korean Society for Molecular and Cellular Biology.

Expression and Imprinting Analysis of AK044800, a Transcript from the Dlk1-Dio3 Imprinted Gene Cluster during Mouse Embryogenesis

Zhengbin Han, Qi Liu, Zhijun Huang, Wei Cui, Yijun Tian, Weili Yan, and Qiong Wu

School of Life Science and Technology, Harbin Institute of Technology, Science Park of Harbin Institute of Technology, Harbin, China

Received: October 19, 2013; Revised: January 25, 2013; Accepted: February 4, 2013

Abstract

Recent advances of induced pluripotent stem cells (iPSCs) has demonstrated that full development potential is closely related with the expression state of noncoding RNAs (ncRNAs) of the Dlk1-Dio3 imprinted gene cluster. However, few of them, especially the long noncoding RNAs (lncRNAs), have been characterized in detail. AK044800 is a transcript from the Dlk1-Dio3 imprinted region with little known information. This study reports original data on the expression pattern of AK044800 during embryogenesis. Expression analysis showed that AK044800 was specifically expressed in the brain at mid-gestation, E9.5 and E11.5. And at E15.5, its expression was mainly concentrated in the forebrain. In the late-gestation stage (E18.5), AK044800 expression was weaker in the brain and began to emerge in some other tissues during this period. Notably, the expression of AK044800 was biallelic in the brain, unlike other noncoding transcripts from this imprinted region. In addition, its expression was dependent on inbred mouse strains. This may be the first lncRNA that has been identified with a different expression between inbred mouse strains. This study may provide useful clues for
further investigations of expression regulation and functions of lncRNAs of the Dlk1-Dio3 imprinted region.

Keywords: AK044800, expression patterns, imprinting analysis, inbred mouse strains, long noncoding RNAs

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.

Supplementary File

Share this article on

  • line

Related articles in Mol. Cells

Molecules and Cells

eISSN 0219-1032
qr-code Download