| Literature DB >> 17622584 |
Scott A Akker1, Shivani Misra, Shazad Aslam, Emma L Morgan, Philip J Smith, Bernard Khoo, Shern L Chew.
Abstract
Pseudoexons occur frequently in the human genome. This paper characterizes a pseudoexon in the GH receptor gene. Inappropriate activation of this pseudoexon causes Laron syndrome. Using in vitro splicing assays, pseudoexon silencing was shown to require a combination of a weak 5' pseudosplice-site and splicing silencing elements within the pseudoexon. Immunoprecipitation experiments showed that specific binding of heterogenous nuclear ribonucleoprotein E1 (hnRNP E1) and U1 small nuclear ribonucleoprotein (snRNP) in the pre-spliceosomal complex was associated with silencing of pseudoexon splicing. The possible role of hnRNP E1 was further supported by RNA interference experiments in cultured cells. Immunoprecipitation experiments with three other pseudoexons suggested that pre-spliceosomal binding of U1 snRNP is a potential general mechanism of suppression of pseudoexons.Entities:
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Year: 2007 PMID: 17622584 DOI: 10.1210/me.2007-0038
Source DB: PubMed Journal: Mol Endocrinol ISSN: 0888-8809