Page 41 - Read Online
P. 41

Page 6 of 11                    Zhang et al. Ageing Neur Dis 2022;2:16  https://dx.doi.org/10.20517/and.2022.15

               Table 2. Summary of genetically modified rabbits
                System   Genes             Modification   Application                                 Refs.
                ZFN      IgM               KO             Immunodeficiency                            [48]
                ZFN      APOC3             KO             Lipid metabolism and                        [49]
                                                          atherosclerosis
                                                                                                      [50]
                ZFN      APOE              KO             Lipid metabolism and
                                                          atherosclerosis
                                                                                                      [51]
                ZFN      CETP              KO             Lipid metabolism and
                                                          atherosclerosis
                                                                                                      [52]
                TALENs   RAG1; RAG2        KO             Immunodeficiency
                                                                                                      [53]
                TALENs   FAH               KO             Hereditary tyrosinemia type 1
                                                                                                      [54]
                CRISPR/Cas9 FBN1           KO             Marfanoid progeroid lipodystrophy syndrome
                                                                                                      [55]
                CRISPR/Cas9 DMD            KO             Duchenne muscular dystrophy
                                                                                                      [56]
                CRISPR/Cas9 ANO5           KO             Muscular dystrophy
                                                                                                      [57]
                CRISPR/Cas9 α-Crystallin   KO             Congenital cataracts
                                                                                                      [58]
                CRISPR/Cas9 GJA8           KO             Congenital cataracts
                                                                                                      [59]
                CRISPR/Cas9 LDLR           KO             Lipid metabolism and
                                                          atherosclerosis
                                                                                                      [60,61]
                CRISPR/Cas9 MSTN           KO             Muscle hypertrophy
                                                                                                      [53,54]
                CRISPR/Cas9 SRY            KO             Sex reversal syndromes and
                                                          hermaphroditism syndromes
                                                                                                      [62]
                CRISPR/Cas9 PHEX           KO             X-linked hypophosphatemia
                                                                                                      [63]
                CRISPR/Cas9 LMNA           KO             Premature aging syndrome
                                                                                                      [64]
                CRISPR/Cpf1  WRN           KO             Werner syndrome
                                                                                                      [65,66]
                CRISPR/Cas9 TYR            KO             Oculocutaneous albinism
                                                                                                      [67]
                CRISPR/Cas9 DMP1           KO             Mineralization defects
                                                                                                      [68]
                CRISPR/Cas9 GADD45G        KO             Congenital cleft palate
                                                                                                      [69]
                CRISPR/Cas9 HOXC13         KO             Hair and nail ectodermal dysplasia
                                                                                                      [70]
                CRISPR/Cas9 GCK            KO             Maturity-onset diabetes of the young type 2
                                                                                                      [71]
                CRISPR/Cas9 HBB2           KO             β-thalassemia
                                                                                                      [72]
                CRISPR/Cas9 WAS            KO             Wiskott-Aldrich syndrome
                                                                                                      [73]
                CRISPR/Cas9 CBS            KO             Congenital hyper-homocysteinemia
                                                                                                      [74]
                CRISPR/Cas9 LDLR; APOE     KO             Lipid metabolism and
                                                          atherosclerosis
                                                                                                      [75]
                CRISPR/Cas9 APOC3          KO             Lipid metabolism and
                                                          atherosclerosis
                                                                                                      [76]
                CRISPR/Cas9 CFTR           KO             Cystic fibrosis
                                                                                                      [77]
                CRISPR/Cas9 CFTR           KO ΔF508       Cystic fibrosis
                                                                                                      [69]
                CRISPR/Cas9 CLPG           KO             Muscular hypertrophy syndrome
                                                                                                      [78]
                CRISPR/Cas9 FGF5           KO             Long hair
                                                                                                      [79]
                CRISPR/Cas9 IL2RG          KO             X-linked severe combined
                                                          immunodeficiency
                                                                                                      [80]
                CRISPR/Cas9 MC1R           KO             Block the synthesis of eumelanin and create a novel pale-yellow coat
                                                          color
                                                                                                      [73]
                CRISPR/Cas9 XIST P1        KO             X-chromosome inactivation
                                                                                                      [74]
                CRISPR/Cas9 MSTN           KO             Muscle hypertrophy
                                                                                                      [75]
                CRISPR/Cas9 PCSK9          p.S386A        Lipid metabolism and
                                                          atherosclerosis
                                                                                                      [81]
                CRISPR/Cas9 ATP7B          p. R778L       Wilson Disease
                                                                                                      [82]
                CRISPR/Cas9 TYR            p. T373K       Oculocutaneous albinism
                                                                                                      [83]
                CRISPR/Cas9 TYR            KO             Oculocutaneous albinism
                                                                                                      [84-86]
                CRISPR/Cas9 RAG; RAG2; TIKI1; ALB;   Multiplex gene KO  Immunodeficiency
                         IL2RG
                CRISPR/Cas9 FUT1; FUT2; SEC1  KO          Fucosyltransferases enzymes activity        [87]
   36   37   38   39   40   41   42   43   44   45   46