Transcripts from a novelBMPR2termination mutation escape nonsense mediated decay by downstream translation re-initiation: implications for treating pulmonary hypertension
| Autor: | John A. Phillips, Joy D. Cogan, Rizwan Hamid, Lora K. Hedges, James E. Loyd, Eric D. Austin |
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| Rok vydání: | 2010 |
| Předmět: |
Male
Genetics Mutation Messenger RNA Hypertension Pulmonary Kozak consensus sequence Nonsense-mediated decay Biology Gene mutation Bone Morphogenetic Protein Receptors Type II medicine.disease_cause Article Pedigree Aminoglycosides Eukaryotic translation Codon Nonsense medicine Humans Female Bone morphogenetic protein receptor Lymphocytes Haploinsufficiency Genetics (clinical) |
| Zdroj: | Clinical Genetics. 77:280-286 |
| ISSN: | 1399-0004 0009-9163 |
| Popis: | Bone morphogenetic protein receptor type 2 (BMPR2 ) gene mutations are a major risk factor for heritable pulmonary arterial hypertension (HPAH), an autosomal dominant fatal disease. We have previously shown that BMPR2 transcripts that contain premature termination codon (PTC) mutations are rapidly and nearly completely degraded through nonsense mediated decay (NMD). Here we report a unique PTC mutation (W13X) that did not behave in the predicted manner. We found that patient-derived cultured lymphocytes (CLs) contained readily detectable levels of the PTC-containing transcript. Further analysis suggested that this transcript escaped NMD by translational re-initiation at a downstream Kozak sequence, resulting in the omission of 173 amino acids. Treatment of CLs containing the PTC with an aminoglycoside decreased the truncated protein levels, with a reciprocal increase in full-length BMPR2 protein and, importantly, BMPR-II signaling. This is the first demonstration of aminoglycoside-mediated ‘repair’ of a BMPR2 mutation at the protein level in patient-derived cells and has obvious implications for treatment of HPAH where no disease-specific treatment options are available. Our data also suggest the need for a more thorough characterization of mutations prior to labeling them as haploinsufficient or dominant negative based simply on sequencing data. |
| Databáze: | OpenAIRE |
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