Airn Transcriptional Overlap, But Not Its lncRNA Products, Induces Imprinted Igf2r Silencing

Author:

Latos Paulina A.1,Pauler Florian M.1,Koerner Martha V.1,Şenergin H. Başak1,Hudson Quanah J.1,Stocsits Roman R.2,Allhoff Wolfgang1,Stricker Stefan H.1,Klement Ruth M.1,Warczok Katarzyna E.1,Aumayr Karin2,Pasierbek Pawel3,Barlow Denise P.1

Affiliation:

1. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, 1090 Vienna, Austria.

2. Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, 1030 Vienna, Austria.

3. Institute of Molecular Biotechnology, Dr. Bohr-Gasse 3, 1030 Vienna, Austria.

Abstract

Long Noncoding RNAs The past 5 years have uncovered thousands of long (>100 nucleotides) noncoding RNAs (lncRNAs) outpacing our understanding of their functions and mechanisms in regulating the genome. Lee (p. 1435 ) reviews the known and suspected means by which these intriguing molecules control gene expression locally and at great distances, considers potential universal roles for lncRNAs, and warns that classifying these intriguing molecules may be quite challenging given their diversity. The very long noncoding RNA, Airn , silences the Igf2r (insulin-like growth factor 2 receptor) imprinted gene cluster in mammals. Latos et al. (p. 1469 ) show in mouse cells that, rather than recruiting enzymes that modify histones to repress the locus, it is the act of transcription of Airn (and not the Airn gene product) that results in the silencing.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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