Context-Dependent Strategies for Enhanced Genome Editing of Genodermatoses

被引:30
作者
March, Oliver Patrick [1 ]
Kocher, Thomas [1 ]
Koller, Ulrich [1 ]
机构
[1] Paracelsus Med Univ Salzburg, Univ Hosp, EB House Austria, Res Program Mol Therapy Genodermatoses,Dept Derma, A-5020 Salzburg, Austria
关键词
genome editing; genodermatoses; designer nucleases; DNA repair pathways; epidermolysis bullosa; keratinopathies; TERMINATION CODON MUTATION; PLURIPOTENT STEM-CELLS; EPIDERMOLYSIS-BULLOSA; DNA-REPAIR; MUSCULAR-DYSTROPHY; GENE CORRECTION; COL7A1; MUTATION; CRISPR/CAS9; BASE; EXON;
D O I
10.3390/cells9010112
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The skin provides direct protection to the human body from assault by the harsh external environment. The crucial function of this organ is significantly disrupted in genodermatoses patients. Genodermatoses comprise a heterogeneous group of largely monogenetic skin disorders, typically involving mutations in genes encoding structural proteins. Therapeutic options for this debilitating group of diseases, including epidermolysis bullosa, primarily consist of wound management. Genome editing approaches co-opt double-strand break repair pathways to introduce desired sequence alterations at specific loci. Rapid advances in genome editing technologies have the potential to propel novel genetic therapies into the clinic. However, the associated phenotypes of many mutations may be treated via several genome editing strategies. Therefore, for potential clinical applications, implementation of efficient approaches based upon mutation, gene and disease context is necessary. Here, we describe current genome editing approaches for the treatment of genodermatoses, along with a discussion of the optimal strategy for each genetic context, in order to achieve enhanced genome editing approaches.
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页数:20
相关论文
共 102 条
[1]   Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy [J].
Amoasii, Leonela ;
Long, Chengzu ;
Li, Hui ;
Mireault, Alex A. ;
Shelton, John M. ;
Sanchez-Ortiz, Efrain ;
McAnally, John R. ;
Bhattacharyya, Samadrita ;
Schmidt, Florian ;
Grimm, Dirk ;
Hauschka, Stephen D. ;
Bassel-Duby, Rhonda ;
Olson, Eric N. .
SCIENCE TRANSLATIONAL MEDICINE, 2017, 9 (418)
[2]   Search-and-replace genome editing without double-strand breaks or donor DNA [J].
Anzalone, Andrew V. ;
Randolph, Peyton B. ;
Davis, Jessie R. ;
Sousa, Alexander A. ;
Koblan, Luke W. ;
Levy, Jonathan M. ;
Chen, Peter J. ;
Wilson, Christopher ;
Newby, Gregory A. ;
Raguram, Aditya ;
Liu, David R. .
NATURE, 2019, 576 (7785) :149-+
[3]   Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis [J].
Arin, M. J. ;
Oji, V. ;
Emmert, S. ;
Hausser, I. ;
Traupe, H. ;
Krieg, T. ;
Grimberg, G. .
BRITISH JOURNAL OF DERMATOLOGY, 2011, 164 (02) :442-447
[4]   Traceless Targeting and Isolation of Gene- Edited Immortalized Keratinocytes from Epidermolysis Bullosa Simplex Patients [J].
Aushev, Magomet ;
Koller, Ulrich ;
Mussolino, Claudio ;
Cathomen, Toni ;
Reichelt, Julia .
MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 2017, 6 :112-123
[5]   Closure of a Large Chronic Wound through Transplantation of Gene-Corrected Epidermal Stem Cells [J].
Bauer, Johann W. ;
Koller, Josef ;
Murauer, Eva M. ;
De Rosa, Laura ;
Enzo, Elena ;
Carulli, Sonia ;
Bondanza, Sergio ;
Recchia, Alessandra ;
Muss, Wolfgang ;
Diem, Anja ;
Mayr, Elisabeth ;
Schlager, Pamina ;
Gratz, Iris K. ;
Pellegrini, Graziella ;
De Luca, Michele .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2017, 137 (03) :778-781
[6]   CRISPR/Cas9-Mediated In Situ Correction of LAMB3 Gene in Keratinocytes Derived from a Junctional Epidermolysis Bullosa Patient [J].
Benati, Daniela ;
Miselli, Francesca ;
Cocchiarella, Fabienne ;
Patrizi, Clarissa ;
Carretero, Marta ;
Baldassarri, Samantha ;
Ammendola, Virginia ;
Has, Cristina ;
Colloca, Stefano ;
Del Rio, Marcela ;
Larcher, Fernando ;
Recchia, Alessandra .
MOLECULAR THERAPY, 2018, 26 (11) :2592-2603
[7]   The Dissolution of Double Holliday Junctions [J].
Bizard, Anna H. ;
Hickson, Ian D. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2014, 6 (07)
[8]   Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing [J].
Bonafont, Jose ;
Mencia, Angeles ;
Garcia, Marta ;
Torres, Raul ;
Rodriguez, Sandra ;
Carretero, Marta ;
Chacon-Solano, Esteban ;
Modamio-Hoybjor, Silvia ;
Marinas, Lucia ;
Leon, Carlos ;
Escamez, Maria J. ;
Hausser, Ingrid ;
Del Rio, Marcela ;
Murillas, Rodolfo ;
Larcher, Fernando .
MOLECULAR THERAPY, 2019, 27 (05) :986-998
[9]   RNA-based therapies for genodermatoses [J].
Bornert, Olivier ;
Peking, Patricia ;
Bremer, Jeroen ;
Koller, Ulrich ;
van den Akker, Peter C. ;
Aartsma-Rus, Annemieke ;
Pasmooij, Anna M. G. ;
Murauer, Eva M. ;
Nystroem, Alexander .
EXPERIMENTAL DERMATOLOGY, 2017, 26 (01) :3-10
[10]  
Bremer Jeroen, 2016, Mol Ther Nucleic Acids, V5, pe379, DOI 10.1038/mtna.2016.87