遺傳學專家詹妮弗．道娜與同事共同發明了一種突破性的新技術「基因編輯技術」，被稱為CRISPR-Cas9。該工具允許科學家們對DNA進行精確的編輯，這可能對遺傳性疾病的治療有幫助......但也可能會被用來創造所謂的「訂製嬰兒」。 道娜展示了CRISPR-Cas9工作原理——並要求科學界停下來討論這個新工具的道德與原則問題。

我們現在可以編輯我們的DNA，但讓我們明智地使用它

CRISPR-Cas9 makes editing DNA as simple as cutting and pasting text, transforming genetic engineering from a painstaking process into a programmable tool. With results like removing HIV from human cells and altering the color of mouse coats with a single gene tweak, its power is undeniable. This technology could cure diseases like cystic fibrosis and sickle cell anemia, but it also opens the door to designer genetics and unprecedented ethical questions. Scientists now face a choice: harness this breakthrough with wisdom, or risk unintended consequences for generations.

CRISPR Unleashes Precision Gene Editing—And Ethical Dilemmas

The Promising and Perilous Science of Gene Editing

On Human Gene Editing: International Summit Statement

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CRISPR

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TED Stage Talk

詹妮弗．道娜: 我們現在可以編輯我們的DNA，但讓我們明智地使用它