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第46卷第1期         马 金,沈     滟,沈国民,等. F9基因剪接位点共识区域中内含子突变造成的异常剪接模式
                  2026年1月                   研究[J]. 南京医科大学学报(自然科学版),2026,46(1):55-67                    · 61   ·


                                   表4 突变对应的临床患者信息及生物信息学预测和微型基因剪接实验结果
                Table 4  Clinical patient information and bioinformatics prediction as well as minigene splicing assay results corresponding
                        to variations

                                  FⅨ variant database            In silico analysis            Minigene assay
                  Mutation
                          Domain Case Severity FⅨ:C FⅨ:Ag HSF(%) MES(%)        RDDC       Transcript  Protein change
                c.278⁃1G>T  Intron 3  2  2S    <1   NA   SA broken SA broken  Insert 168 nt  Exon skipping p.G94⁃D131del
                                                         (-35.57)(-167.32)    intron 3  96 nt deletion  p.D93⁃
                                                                            Exon skipping  of exon 4  G125delinsG
                c.278⁃1G>C  Intron 3  1  1S    <1   <1   SA broken SA broken  Insert 168 nt  Exon skipping p.G94⁃D131del
                                                         (-35.57) (-157)      intron 3  96 nt deletion  p.D93⁃
                                                                            Exon skipping  of exon 4  G125delinsG
                c.278⁃1G>A Intron 3  2  1Mo   -3-   NA   SA broken SA broken  Insert 168 nt  Exon skipping p.G94⁃D131del
                                                         (-35.57)(-170.23)    intron 3  96 nt deletion  p.D93⁃
                                                                            Exon skipping  of exon 4  G125delinsG
                c.278⁃2A>T  Intron 3  2  2S    <1   NA   SA broken SA broken Insert 6 nt intron 3 Exon skipping p.G94⁃D131del
                                                         (-35.57)(-162.84) Exonskipping  96 nt deletion  p.D93⁃
                                                                                          of exon 4  G125delinsG
                c.278⁃3A>G Intron 3  8  7S,1Mo  <1  NA    New SA   New SA Insert 2 nt intron 3 2 nt retention  p.D93fsTer12
                                                         (+55.07)(+227.53) Exonskipping   of intron 3
                                                            No    SA broken
                                                                 (-147.08)
                c.391delG  Exon 4  1    1Mo   2.04  NA    New SA   New SA   WT premature  WT premature p.D131MfsTer2
                                                        (+122.42)(+131.98) Exon skipping  Exon skipping p.G94⁃D131del
                                                          New SA     No
                                                         (+67.78) SA broken
                                                         SA broken (-241.51)
                                                         (-74.9)
                c.391+1G>T Intron 4  6  6S    <0-1  NA   SD broken SD broken    NT      Exon skipping p.G94⁃D131del
                                                         (-27.56) (-85.61)
                c.391+1G>A Intron 4  3  3Mo  1-1.2  <1   SD broken SD broken Insert 4 nt intron 4 Exon skipping p.G94⁃D131del
                                                         (-27.56) (-87.99)  Exonskipping
                                                                                NT
                c.391+1G>C Intron 4  4  2S,1Mo -0.8-  27  SD broken SD broken Insert 4 nt intron 4 Exon skipping p.G94⁃D131del
                                                         (-27.56) (-84.68)  Exonskipping
                                                                                NT
                c.391+1insT Intron 4  1  1S    <1   NA   SD broken SD broken    No      WT premature p.D131VfsTer5
                                                        (-318.13)(-154.06)              Exon skipping p.G94⁃D131del
                c.391+2T>A Intron 4  1  NA    NA    NA   SD broken SD broken Insert 4 nt intron 4 Exon skipping p.G94⁃D131del
                                                         (-27.56) (-84.68)  Exonskipping
                                                                                NT
                c.391+2T>C Intron 4  4  3Mo   8-20  NA   SD broken SD broken    NT      Exon skipping p.G94⁃D131del
                                                         (-27.56) (-80.23)
                c.391+5G>A Intron 4  3  1Mo   -5-   NA      No    SD broken     NT      Exon skipping p.G94⁃D131del
                                                                  (-31.47)                  NT          WT
                c.391+5delG Intron 4  1  NA   NA    NA   SD broken   No         NT      Exon skipping p.G94⁃D131del
                                                         (-12.56)
                c.391+7A>G Intron 4  7  5S,2Mo <1-4  <1⁃3   No       No         NT      Exon skipping p.G94⁃D131del
                                                                                            NT          WT
                   S indicates severe;Mo indicates moderate;NA indicates no available data;SA indicates splice acceptor;SD indicates splice donor. Numbers repre⁃
                sent changes relative to the original score;“-”denotes a decrease and“+”denotes an increase. NT indicates normal transcript;WT indicates wild⁃type;
                del indicates deletion;fs indicates frameshift;“No”indicates no effect on splicing.

                而,c.391delG 和 c.391+1insT 突变产生了两种转录               存在外显子跳跃(258 bp)现象。值得注意的是,其
                本:一种与 WT 大小相似(372 bp),另一种提示可能                     余 11 个突变(73.3%)均产生了单一的异常剪接产
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