Box C/D small nucleolar RNA genes and the Prader‐Willi syndrome: a complex interplay

Abstract

The nucleolus of mammalian cells contains hundreds of box C/D small nucleolar RNAs(SNORDs). Through their ability to base pair with ribosomal RNA precursors, most play important roles in the synthesis and/or activity of ribosomes, either by guiding sequence‐specific 2′‐O‐methylations or by facilitating RNA folding and cleavages. A growing number of SNORD genes with elusive functions have been discovered recently. Intriguingly, the vast majority of them are located in two large, imprinted gene clusters at human chromosome region 15q11q13 (theSNURF–SNRPNdomain) and at 14q32 (theDLK1–DIO3domain) where they are expressed, respectively, only from the paternally and maternally inherited alleles. These placental mammal‐specific SNORD genes have many features of the canonical SNORDs that guide 2′‐O‐methylations, yet they lack obvious complementarity with ribosomal RNAs and, surprisingly, they are processed from large, tandemly repeated genes expressed preferentially in the brain. This review summarizes our understanding of the biology of these peculiar SNORD genes, focusing particularly onSNORD115andSNORD116in theSNURF–SNRPNdomain. It examines the growing evidence that altered levels of these SNORDs and/or their host‐gene transcripts may be a primary cause of Prader‐Willi syndrome (PWS; a rare disorder characterized by overeating and obesity) as well as abnormalities in signaling through the 5‐HT2C serotonin receptor. Finally, the hypothesis that PWS may be a ribosomopathy (ribosomal disease) is also discussed.WIREs RNA 2017, 8:e1417. doi: 10.1002/wrna.1417 This article is categorized under:Translation > Ribosome Biogenesis RNA Processing > RNA Editing and Modification RNA in Disease and Development > RNA in Disease