Ontology highlight
ABSTRACT:
SUBMITTER: Falaleeva M
PROVIDER: S-EPMC5586535 | biostudies-literature | 2015 Nov
REPOSITORIES: biostudies-literature
Falaleeva Marina M Surface Justin J Shen Manli M de la Grange Pierre P Stamm Stefan S
Gene 20150726 2
The loss of two gene clusters encoding small nucleolar RNAs, SNORD115 and SNORD116 contribute to Prader-Willi syndrome (PWS), the most common syndromic form of obesity in humans. SNORD115 and SNORD116 are considered to be orphan C/D box snoRNAs (SNORDs) as they do not target rRNAs or snRNAs. SNORD115 exhibits sequence complementarity towards the serotonin receptor 2C, but SNORD116 shows no extended complementarities to known RNAs. To identify molecular targets, we performed genome-wide array ana ...[more]