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|Title:||Systemic splicing factor deficiency causes tissue-specific defects: A zebrafish model for retinitis pigmentosa||Authors:||Linder, B.
|Issue Date:||Jan-2011||Citation:||Linder, B., Dill, H., Hirmer, A., Brocher, J., Lee, G.P., Mathavan, S., Bolz, H.J., Winkler, C., Laggerbauer, B., Fischer, U. (2011-01). Systemic splicing factor deficiency causes tissue-specific defects: A zebrafish model for retinitis pigmentosa. Human Molecular Genetics 20 (2) : 368-377. ScholarBank@NUS Repository. https://doi.org/10.1093/hmg/ddq473||Abstract:||Retinitis pigmentosa (RP) is a common hereditary eye disease that causes blindness due to a progressive loss of photoreceptors in the retina. RP can be elicited by mutations that affect the tri-snRNP subunit of the premRNA splicing machinery, but how defects in this essential macromolecular complex transform into a photoreceptor-specific phenotype is unknown. Wehavemodeled the disease in zebrafish by silencing the RP-associated splicing factor Prpf31 and observed detrimental effects on visual function and photoreceptor morphology. Despite reducing the level of a constitutive splicing factor, no general defects in gene expression were found. Instead, retinal genes were selectively affected, providing the first in vivo link between mutations in splicing factors and the RP phenotype. Silencing of Prpf4, a splicing factor hitherto unrelated to RP, evoked the same defects in vision, photoreceptor morphology and retinal gene expression. Hence, various routes affecting the tri-snRNP can elicit tissue-specific gene expression defects and lead to the RP phenotype. © The Author 2010. Published by Oxford University Press. All rights reserved.||Source Title:||Human Molecular Genetics||URI:||http://scholarbank.nus.edu.sg/handle/10635/101810||ISSN:||09646906||DOI:||10.1093/hmg/ddq473|
|Appears in Collections:||Staff Publications|
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