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dc.contributor.authorLisa Riedmayr
dc.contributor.authorSybille Böhm
dc.contributor.authorStylianos Michalakis
dc.contributor.authorElvir Becirovic
dc.contributor.otherCenter for Integrated Protein Science Munich CIPSM, München, GermanyDepartment of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, München, Germany
dc.contributor.otherCenter for Integrated Protein Science Munich CIPSM, München, GermanyDepartment of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, München, Germany
dc.contributor.otherCenter for Integrated Protein Science Munich CIPSM, München, GermanyDepartment of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, München, Germany
dc.contributor.otherCenter for Integrated Protein Science Munich CIPSM, München, GermanyDepartment of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, München, Germany
dc.date.accessioned2024-06-05T01:57:10Z
dc.date.accessioned2025-10-08T08:47:33Z
dc.date.available2025-10-08T08:47:33Z
dc.date.issued01-03-2018
dc.identifier.urihttp://digilib.fisipol.ugm.ac.id/repo/handle/15717717/37256
dc.description.abstractDisease-associated mutations influencing mRNA splicing are referred to as splice mutations. The majority of splice mutations are found on exon-intron boundaries defining canonical donor and acceptor splice sites. However, mutations in the coding region (exonic mutations) can also affect mRNA splicing. Exact knowledge of the disease mechanism of splice mutations is essential for developing optimal treatment strategies. Given the large number of disease-associated mutations thus far identified, there is an unmet need for methods to systematically analyze the effects of pathogenic mutations on mRNA splicing. As splicing can vary between cell types, splice mutations need to be tested under native conditions if possible. A commonly used tool for the analysis of mRNA splicing is the construction of minigenes carrying exonic and intronic sequences. Here, we describe a protocol for the design and cloning of minigenes into recombinant adeno-associated virus (rAAV) vectors for gene delivery and investigation of mRNA splicing in a native context. This protocol was developed for minigene-based analysis of mRNA splicing in retinal cells, however, in principle it is applicable to any cell type, which can be transduced with rAAV vectors.
dc.language.isoEN
dc.publisherBio-protocol LLC
dc.subject.lccBiology (General)
dc.titleConstruction and Cloning of Minigenes for in vivo Analysis of Potential Splice Mutations
dc.typeArticle
dc.description.doi10.21769/BioProtoc.2760
dc.title.journalBio-Protocol
dc.identifier.e-issn2331-8325
dc.identifier.oaioai:doaj.org/journal:a9c0e393d91d4a1787dd1a36af2b7bba
dc.journal.infoVolume 8, Issue 5


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