In a story of scientific discovery, chemical biologist David R. Liu shares a breakthrough: his lab’s development of base editors that can rewrite DNA. This crucial step in genome editing takes the promise of CRISPR to the next level: if CRISPR proteins are molecular scissors, programmed to cut specific DNA sequences, then base editors are pencils, capable of directly rewriting one DNA letter into another. Learn more about how these molecular machines work — and their potential to treat or even cure genetic diseases.

科学的発見の物語の中で、化学生物学者のデビッド R. リューは、DNA を書き換えることができる塩基エディターの研究室の開発という画期的な発見を共有しています。

ゲノム編集におけるこの重要なステップは、CRISPR の期待を次のレベルに引き上げます。

CRISPR タンパク質が特定の DNA 配列を切断するようにプログラムされた分子ハサミであるとすれば、ベースエディターは鉛筆であり、ある DNA 文字を別の DNA 文字に直接書き換えることができます。これらの分子機械がどのように機能するか、そして遺伝性疾患を治療したり治癒したりする可能性について詳しく学びましょう。

タイトル Can we cure genetic diseases by rewriting DNA?
アップロード 2019年5月22日
キャスト デビッド R. リュー

「Can we cure genetic diseases by rewriting DNA?(DNAを書き換えることで遺伝病を治療できるのでしょうか?)」の文字起こし



  • 親から受け継ぐ最も重要な贈り物は、ゲノムを構成する30億のDNA文字です。これらのDNA文字は私たちの体の基本的な設計図であり、個々の特性や健康状態を決定します。これらの遺伝情報は親から子へと受け継がれ、生命の継続性を支えます。


  • DNAで最も一般的な変化は、1文字の単純な置換であり、これをポイントミューテーションと呼びます。ポイントミューテーションは、DNAの一部が異なる塩基に置き換わることで発生します。これらの変異の多くは無害ですが、一部は有害で、遺伝性疾患やがんなどの原因となります。


  • ベースエディティングという技術が開発され、特定のポイントミューテーションを修正することが可能になりました。ベースエディティングは、CRISPR技術を応用して特定のDNA塩基を別の塩基に変換する分子機械です。これにより、遺伝性疾患の原因となる特定のミューテーションを修正することが可能となり、治療の新しい可能性が開かれました。


  • ベースエディティングは既に動物モデルで遺伝性疾患の治療に成功しています。鎌状赤血球症や早老症などの遺伝性疾患を持つ動物モデルにおいて、ベースエディティングを用いて病原性ミューテーションを修正することに成功しています。この技術は今後、人間の遺伝性疾患治療にも応用される可能性があります。


The most important gift your mother and father ever gave you was the two sets of three billion letters of DNA that make up your genome. But like anything with three billion components, that gift is fragile. Sunlight, smoking, unhealthy eating, even spontaneous mistakes made by your cells, all cause changes to your genome.

The most common kind of change in DNA is the simple swap of one letter, or base, such as C, with a different letter, such as T, G or A. In any day, the cells in your body will collectively accumulate billions of these single-letter swaps, which are also called “point mutations.” Now, most of these point mutations are harmless. But every now and then, a point mutation disrupts an important capability in a cell or causes a cell to misbehave in harmful ways.

If that mutation were inherited from your parents or occurred early enough in your development, then the result would be that many or all of your cells contain this harmful mutation. And then you would be one of hundreds of millions of people with a genetic disease, such as sickle cell anemia or progeria or muscular dystrophy or Tay-Sachs disease. Grievous genetic diseases caused by point mutations are especially frustrating because we often know the exact single-letter change that causes the disease and, in theory, could cure the disease.

Millions suffer from sickle cell anemia because they have a single A to T point mutations in both copies of their hemoglobin gene. And children with progeria are born with a T at a single position in their genome where you have a C, with the devastating consequence that these wonderful, bright kids age very rapidly and pass away by about age 14. Throughout the history of medicine, we have not had a way to efficiently correct point mutations in living systems, to change that disease-causing T back into a C. Perhaps until now.

Because my laboratory recently succeeded in developing such a capability, which we call “base editing.” The story of how we developed base editing actually begins three billion years ago. We think of bacteria as sources of infection, but bacteria themselves are also prone to being infected, in particular, by viruses. So about three billion years ago, bacteria evolved a defense mechanism to fight viral infection. That defense mechanism is now better known as CRISPR. And the warhead in CRISPR is this purple protein that acts like molecular scissors to cut DNA, breaking the double helix into two pieces.

If CRISPR couldn’t distinguish between bacterial and viral DNA, it wouldn’t be a very useful defense system. But the most amazing feature of CRISPR is that the scissors can be programmed to search for, bind to and cut only a specific DNA sequence. So when a bacterium encounters a virus for the first time, it can store a small snippet of that virus’s DNA for use as a program to direct the CRISPR scissors to cut that viral DNA sequence during a future infection. Cutting a virus’s DNA messes up the function of the cut viral gene and therefore disrupts the virus’s life cycle.

Remarkable researchers including Emmanuelle Charpentier, George Church, Jennifer Doudna and Feng Zhang showed six years ago how CRISPR scissors could be programmed to cut DNA sequences of our choosing, including sequences in your genome, instead of the viral DNA sequences chosen by bacteria. But the outcomes are actually similar. Cutting a DNA sequence in your genome also disrupts the function of the cut gene, typically, by causing the insertion and deletion of random mixtures of DNA letters at the cut site. Now, disrupting genes can be very useful for some applications. But for most point mutations that cause genetic diseases, simply cutting the already-mutated gene won’t benefit patients, because the function of the mutated gene needs to be restored, not further disrupted.

So cutting this already-mutated hemoglobin gene that causes sickle cell anemia won’t restore the ability of patients to make healthy red blood cells. And while we can sometimes introduce new DNA sequences into cells to replace the DNA sequences surrounding a cut site, that process, unfortunately, doesn’t work in most types of cells, and the disrupted gene outcomes still predominate. Like many scientists, I’ve dreamed of a future in which we might be able to treat or maybe even cure human genetic diseases. But I saw the lack of a way to fix point mutations, which cause most human genetic diseases, as a major problem standing in the way.

Being a chemist, I began working with my students to develop ways on performing chemistry directly on an individual DNA base, to truly fix, rather than disrupt, the mutations that cause genetic diseases. The results of our efforts are molecular machines called “base editors.” Base editors use the programmable searching mechanism of CRISPR scissors, but instead of cutting the DNA, they directly convert one base to another base without disrupting the rest of the gene.

So if you think of naturally occurring CRISPR proteins as molecular scissors, you can think of base editors as pencils, capable of directly rewriting one DNA letter into another by actually rearranging the atoms of one DNA base to instead become a different base. Now, base editors don’t exist in nature. In fact, we engineered the first base editor, shown here, from three separate proteins that don’t even come from the same organism. We started by taking CRISPR scissors and disabling the ability to cut DNA while retaining its ability to search for and bind a target DNA sequence in a programmed manner.

To those disabled CRISPR scissors, shown in blue, we attached a second protein in red, which performs a chemical reaction on the DNA base C, converting it into a base that behaves like T. Third, we had to attach to the first two proteins the protein shown in purple, which protects the edited base from being removed by the cell. The net result is an engineered three-part protein that for the first time allows us to convert Cs into Ts at specified locations in the genome. But even at this point, our work was only half done. Because in order to be stable in cells, the two strands of a DNA double helix have to form base pairs.

And because C only pairs with G, and T only pairs with A, simply changing a C to a T on one DNA strand creates a mismatch, a disagreement between the two DNA strands that the cell has to resolve by deciding which strand to replace. We realized that we could further engineer this three-part protein to flag the nonedited strand as the one to be replaced by nicking that strand. This little nick tricks the cell into replacing the nonedited G with an A as it remakes the nicked strand, thereby completing the conversion of what used to be a C-G base pair into a stable T-A base pair.

After several years of hard work led by a former post doc in the lab, Alexis Komor, we succeeded in developing this first class of base editor, which converts Cs into Ts and Gs into As at targeted positions of our choosing. Among the more than 35,000 known disease-associated point mutations, the two kinds of mutations that this first base editor can reverse collectively account for about 14 percent or 5,000 or so pathogenic point mutations. But correcting the largest fraction of disease-causing point mutations would require developing a second class of base editor, one that could convert As into Gs or Ts into Cs.

Led by Nicole Gaudelli, a former post doc in the lab, we set out to develop this second class of base editor, which, in theory, could correct up to almost half of pathogenic point mutations, including that mutation that causes the rapid-aging disease progeria. We realized that we could borrow, once again, the targeting mechanism of CRISPR scissors to bring the new base editor to the right site in a genome. But we quickly encountered an incredible problem; namely, there is no protein that’s known to convert A into G or T into C in DNA.

Faced with such a serious stumbling block, most students would probably look for another project, if not another research advisor. (Laughter) But Nicole agreed to proceed with a plan that seemed wildly ambitious at the time. Given the absence of a naturally occurring protein that performs the necessary chemistry, we decided we would evolve our own protein in the laboratory to convert A into a base that behaves like G, starting from a protein that performs related chemistry on RNA. We set up a Darwinian survival-of-the-fittest selection system that explored tens of millions of protein variants and only allowed those rare variants that could perform the necessary chemistry to survive.

We ended up with a protein shown here, the first that can convert A in DNA into a base that resembles G. And when we attached that protein to the disabled CRISPR scissors, shown in blue, we produced the second base editor, which converts As into Gs, and then uses the same strand-nicking strategy that we used in the first base editor to trick the cell into replacing the nonedited T with a C as it remakes that nicked strand, thereby completing the conversion of an A-T base pair to a G-C base pair. (Applause)

Thank you. (Applause) As an academic scientist in the US, I’m not used to being interrupted by applause. (Laughter) We developed these first two classes of base editors only three years ago and one and a half years ago. But even in that short time, base editing has become widely used by the biomedical research community. Base editors have been sent more than 6,000 times at the request of more than 1,000 researchers around the globe. A hundred scientific research papers have been published already, using base editors in organisms ranging from bacteria to plants to mice to primates.

While base editors are too new to have already entered human clinical trials, scientists have succeeded in achieving a critical milestone towards that goal by using base editors in animals to correct point mutations that cause human genetic diseases. For example, a collaborative team of scientists led by Luke Koblan and Jon Levy, two additional students in my lab, recently used a virus to deliver that second base editor into a mouse with

progeria, changing that disease-causing T back into a C and reversing its consequences at the DNA, RNA and protein levels.

Base editors have also been used in animals to reverse the consequence of tyrosinemia, beta thalassemia, muscular dystrophy, phenylketonuria, a congenital deafness and a type of cardiovascular disease — in each case, by directly correcting a point mutation that causes or contributes to the disease. In plants, base editors have been used to introduce individual single DNA letter changes that could lead to better crops. And biologists have used base editors to probe the role of individual letters in genes associated with diseases such as cancer.

Two companies I cofounded, Beam Therapeutics and Pairwise Plants, are using base editing to treat human genetic diseases and to improve agriculture. All of these applications of base editing have taken place in less than the past three years: on the historical timescale of science, the blink of an eye. Additional work lies ahead before base editing can realize its full potential to improve the lives of patients with genetic diseases.

While many of these diseases are thought to be treatable by correcting the underlying mutation in even a modest fraction of cells in an organ, delivering molecular machines like base editors into cells in a human being can be challenging. Co-opting nature’s viruses to deliver base editors instead of the molecules that give you a cold is one of several promising delivery strategies that’s been successfully used. Continuing to develop new molecular machines that can make all of the remaining ways to convert one base pair to another base pair and that minimize unwanted editing at off-target locations in cells is very important.

And engaging with other scientists, doctors, ethicists and governments to maximize the likelihood that base editing is applied thoughtfully, safely and ethically, remains a critical obligation. These challenges notwithstanding, if you had told me even just five years ago that researchers around the globe would be using laboratory-evolved molecular machines to directly convert an individual base pair to another base pair at a specified location in the human genome efficiently and with a minimum of other outcomes, I would have asked you, “What science-fiction novel are you reading?”

Thanks to a relentlessly dedicated group of students who were creative enough to engineer what we could design ourselves and brave enough to evolve what we couldn’t, base editing has begun to transform that science-fiction-like aspiration into an exciting new reality, one in which the most important gift we give our children may not only be three billion letters of DNA, but also the means to protect and repair them.

Thank you.


Thank you.