現今已知接近有7萬幾種的基因變異會引起疾病。501Please respect copyright.PENANAjEyiwaancn501Please respect copyright.PENANA1uoGuROYq4
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隨著CRISPR基因編輯技術的興起,將會為根治這些疾病帶來曙光。501Please respect copyright.PENANAXiMMBddZKY
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(圖2)圖中將展示「舊式」的編輯方法HDR(Homology Directed Repair)機制。501Please respect copyright.PENANAkapmMmBFMJ501Please respect copyright.PENANAcBVQOdaXO0
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sgRNA將會引領Cas9蛋白質抵達不理想的基因突變位置,其後Cas9蛋白質會將基因斬斷成兩截;501Please respect copyright.PENANA43OfV2zBqj
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根據Cas9蛋白質的特性,可修改至只斬一條特定的DNA位置,其後會再提及。501Please respect copyright.PENANAZUZbQCIQJX
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(圖3)此時候,如果將盛載想修改的基因排組送到斷成兩截的基因附近,細胞便會加以利用,將原本的紫色區域改成為黃色區域。501Please respect copyright.PENANANIaR2fm6aO501Please respect copyright.PENANAtyfPl7SIzo
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但這個方法的隨機性非常之高,最終結果有可能會出現基因刪減,又或者是其他基因排組的插入。501Please respect copyright.PENANAmLFZdbbVTX
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套用基因編輯技術於治療病人身上的話,精準度必須要非常之高,此手段明顯並不理想。501Please respect copyright.PENANAOLxuMcldk1
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(圖4)至於新式編輯方法Prime Editing方面,同樣亦是套用CRISPR技術,但各組件及理念則有所修改。501Please respect copyright.PENANAo3qTLQ9lY3501Please respect copyright.PENANAwI1R13VoRS
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擁有Transcriptase Domain的Cas9變種蛋白質將會被含有預想修改基因排組的pegRNA引領到不理想的基因突變位置,而這一次只會斬斷特定的一條DNA。501Please respect copyright.PENANA5JNGoiomeT
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(圖5)其後,Cas9變種蛋白質會讀取pegRNA內含的預想修改基因排組,並將一條DNA的基因排組成功修改。501Please respect copyright.PENANAU06paDnbjX501Please respect copyright.PENANAsQhUILh9co
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經過一系列難以深入淺出的程序後,最終亦會完成成功修改雙方兩截的DNA。501Please respect copyright.PENANAN6bymlPPmG
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(圖6)紅色區域為不理想的基因修改結果(Ref2),新式編輯方法PrimeEditing明顯優勝於舊式編輯方法HDR,但仍有一定程度的進步空間。501Please respect copyright.PENANAfmTlj9jy6G501Please respect copyright.PENANA2mm9t2O6xg
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有朝一日,CRISPR基因編輯技術定必會在治療疾病上得以普及化。501Please respect copyright.PENANAvR6Bjko7KK
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Link: https://www.penana.com/story/66244/%E7%A7%91%E6%99%AE%E5%B0%88%E6%AC%84-%E8%96%AF%E4%B8%8D%E6%8F%80%E5%96%AE/toc501Please respect copyright.PENANA4Ld66IMVWm
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https://www.penana.com/user/27349/%E8%96%AF%E4%BB%94%E8%81%9E%E8%8C%B1%E8%8E%89/portfolio501Please respect copyright.PENANAvg8hDjABL1
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Ref1:https://www.nature.com/articles/s41586-019-1711-4501Please respect copyright.PENANA2FkR2O3m6u
Ref2:https://www.nature.com/articles/s41467-020-19136-7
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