\u4e00\u672c\u8bb2\u57fa\u56e0\u7f16\u8f91\u6280\u672f\u53d1\u660e\u4ebaDoudna Jennifer\u548c\u5176\u7ade\u4e89\u8005\u5f20\u5cf0\u7684\u6545\u4e8b\u3002\u57fa\u56e0\u7f16\u8f91\u7684\u53d1\u73b0\u5386\u53f2\u4e0d\u8fc7\u624d\u5341\u5e74\u7684\u65f6\u95f4\uff0c\u4e0b\u6e38\u7684\u5e94\u7528\u8fd8\u5c1a\u672a\u6253\u5f00\uff0c\u4f46\u4f5c\u4e3a\u4e00\u9879\u7a81\u7834\u6027\u7684\u6280\u672f\u503c\u5f97\u957f\u671f\u8ddf\u8e2a\u548c\u5173\u6ce8\uff0c\u8fd9\u6837\u7684\u4e66\u8bfb\u8d77\u6765\u5bf9\u4e8e\u7406\u89e3\u6280\u672f\u548c\u5176\u5c40\u9650\u662f\u76f8\u5f53\u6709\u5e2e\u52a9\u7684\u3002<\/p>\n\n\n\n
It was fitting that a virus-fighting team would be led by a CRISPR pioneer. The gene-editing tool that Doudna and others developed in 2012 is based on a virus-fighting trick used by bacteria<\/strong>, which have been battling viruses for more than a billion years. In their DNA, bacteria develop clustered repeated sequences<\/strong>, known as CRISPRs, that can remember and then destroy viruses that attack them. In other words, it\u2019s an immune system that can adapt itself to fight each new wave of viruses\u2014just what we humans need in an era that has been plagued, as if we were still in the Middle Ages, by repeated viral epidemics.<\/p><\/blockquote>\n\n\n\n
\u57fa\u56e0\u7f16\u8f91\u6280\u672f\u7684\u53d1\u660e\u6e90\u4e8e\u5bf9\u7ec6\u83cc\u9632\u75c5\u6bd2\u653b\u51fb\u6280\u672f\u7684\u53d1\u73b0\uff0c\u662f\u7ec6\u83cc\u5df2\u7ecf\u7528\u4e86\u5341\u4ebf\u5e74\u7684\u6280\u672f\u4e86\u3002\u548c\u7ec6\u83cc\u7684\u8fd9\u4e2a\u5f3a\u5927\u6280\u672f\u76f8\u6bd4\uff0c\u4eba\u7c7b\u4e00\u6b21\u6b21\u6536\u5230\u75c5\u6bd2\u7684\u653b\u51fb\uff0c\u5c31\u50cf\u6d3b\u5728\u4e2d\u4e16\u7eaa\u4e00\u6837\u3002<\/p>\n\n\n\n
The invention of CRISPR and the plague of COVID will hasten our transition to the third great revolution of modern times. These revolutions arose from the discovery, beginning just over a century ago, of the three fundamental kernels of our existence: the atom, the bit, and the gene.<\/p><\/blockquote>\n\n\n\n
\u57fa\u56e0\u7f16\u8f91\u548c\u75ab\u60c5\u5c06\u52a0\u901f\u8fd1\u671f\u7684\u7b2c\u4e09\u6b21\u6280\u672f\u9769\u547d\uff0c\u57fa\u4e8e\u539f\u5b50\/\u80fd\u91cf\u3001\u6bd4\u7279\/\u4fe1\u606f\u3001\u57fa\u56e0\/\u751f\u7269\u7684\u4e09\u5927\u53d1\u73b0\u3002<\/p>\n\n\n\n
\u201cCRISPR evolved in bacteria because of their long-running war against viruses,\u201d Doudna says. \u201cWe humans don\u2019t have time to wait for our own cells to evolve natural resistance to this virus, so we have to use our ingenuity to do that. Isn\u2019t it fitting that one of the tools is this ancient bacterial immune system called CRISPR? Nature is beautiful that way.\u201d <\/p><\/blockquote>\n\n\n\n
Nature is beautiful<\/strong>. \u4eba\u7c7b\u5bf9\u81ea\u7136\u4e16\u754c\u7684\u8ba4\u77e5\u8fd8\u8fdc\u8fdc\u4e0d\u591f\uff0c\u67d0\u79cd\u610f\u4e49\u4e0a\u8fd9\u4e5f\u662f\u9760\u5c71\u5403\u5c71\u3002<\/p>\n\n\n\n
Most of all, I want to convey the importance of basic science, meaning quests that are curiosity-drive<\/strong>n rather than application-oriented. Curiosity-driven research into the wonders of nature plants the seeds, sometimes in unpredictable ways, for later innovations.Research about surface-state physics eventually led to the transistor and microchip. Likewise, studies of an astonishing method that bacteria use to fight off viruses eventually led to a gene-editing tool and techniques that humans can use in their own struggle against viruses.<\/p><\/blockquote>\n\n\n\n
\u57fa\u7840\u79d1\u5b66\u5e94\u8be5\u662f\u597d\u5947\u5fc3\u5bfc\u5411\u7684\u7814\u7a76\uff0c\u800c\u4e0d\u662f\u5e94\u7528\u5bfc\u5411\u7684\u7814\u7a76\u3002<\/p>\n\n\n\n
Many creative people\u2014including most of those I have chronicled, such as Leonardo da Vinci, Albert Einstein, Henry Kissinger, and Steve Jobs\u2014grew up feeling alienated from their surroundings.<\/strong> That was the case for Doudna as a young blond girl among the Polynesians in Hilo. \u201cI was really, really alone and isolated at school,\u201d she says. In the third grade, she felt so ostracized that she had trouble eating. \u201cI had all sorts of digestive problems that I later realized were stress related. Kids would tease me every day.\u201d She retreated into books and developed a defensive layer. \u201cThere\u2019s an internal part of me they\u2019ll never touch,\u201d she told herself.Like many others who have felt like an outsider, she developed a wide-ranging curiosity about how we humans fit into creation<\/strong>.\u201d<\/p><\/blockquote>\n\n\n\n
\u4f17\u591a\u77e5\u540d\u79d1\u5b66\u5bb6\u7ae5\u5e74\u65f6\u90fd\u5f88\u4e0d\u5408\u7fa4\u3002\u56e0\u4e3a\u4e0d\u5408\u7fa4\u8f6c\u800c\u4f1a\u66f4\u6709\u597d\u5947\u5fc3\u3001\u66f4\u52a0\u5173\u6ce8\u81ea\u6211\u548c\u521b\u9020\u3002<\/p>\n\n\n\n
We all see nature\u2019s wonders every day, whether it be a plant that moves or a sunset that reaches with pink fingers into a sky of deep blue. The key to true curiosity is pausing to ponder the causes. What makes a sky blue or a sunset pink or a leaf of sleeping grass curl?<\/p>
Darwin and Wallace realized this could be applied to all species and thus lead to a theory of evolution driven by the survival of the fittest. \u201cI happened to read for amusement Malthus on population, and\u2026 it at once struck me that under these circumstances favorable variations would tend to be preserved and unfavorable ones to be destroyed,\u201d Darwin recalled.<\/p><\/blockquote>\n\n\n\n
\u9020\u7269\u4e3b\u5947\u8ff9\u5176\u5b9e\u5c31\u5728\u773c\u524d\uff0c\u5927\u591a\u6570\u4eba\u53ea\u662f\u7f3a\u5c11\u597d\u5947\u5fc3\u3002\u8fbe\u5c14\u6587\u5f53\u5e74\u7684\u9002\u8005\u751f\u5b58\u7406\u8bba\u4e5f\u4e0d\u4ec5\u662f\u51fa\u81ea\u89c2\u5bdf\u3002<\/p>\n\n\n\n
Watson and Crick finished their paper on the last weekend of March 1953. It was a mere 975 words, typed by Watson\u2019s sister, who was persuaded to do so by his argument that \u201cshe was participating in perhaps the most famous event in biology since Darwin\u2019s book.\u201d Crick wanted to include an expanded section on the implications for heredity, but Watson convinced him that a shorter ending would actually carry more punch. Thus was produced one of the most significant sentences in science: \u201cIt has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material<\/strong>.<\/p><\/blockquote>\n\n\n\n
\u590d\u6742\u57fa\u56e0\u7684\u590d\u5236\u673a\u5236\u5f88\u96be\u8bf4\u4e0d\u662f\u51fa\u81ea\u4e0a\u5e1d\u4e4b\u624b\uff0c\u8fd9\u4e2a\u53d1\u73b0\u4e5f\u5c3170\u5e74\u7684\u65f6\u95f4\u3002<\/p>\n\n\n\n
Two revolutions coincided in the 1950s. Mathematicians, including Claude Shannon and Alan Turing, showed that all information could be encoded by binary digits, known as bits. This led to a digital revolution powered by circuits with on-off switches that processed information. Simultaneously, Watson and Crick discovered how instructions for building every cell in every form of life were encoded by the four-letter sequences of DNA. Thus was born an information age based on digital coding (0100110111001\u2026) and genetic coding (ACTGGTAGATTACA\u2026). The flow of history is accelerated when two rivers converge.<\/p><\/blockquote>\n\n\n\n
50\u5e74\u4ee3\u4fe1\u606f\u548cDNA\u4e24\u4e2a\u4e8c\u8fdb\u5236\u51e0\u4e4e\u540c\u65f6\u53d1\u73b0\uff0c\u4fe1\u606f\u7684\u4e8c\u8fdb\u5236\u5e26\u6765\u4e86\u5168\u9762\u7684\u79d1\u6280\u9769\u547d\u3001\u4fe1\u606f\u9769\u547d\uff0c\u751f\u7269\u7684\u8fd9\u4e2a\u4e8c\u8fdb\u5236\u4e5f\u5c06\u5e26\u6765\u4e00\u573a\u9769\u547d\u3002<\/p>\n\n\n\n
It sparked the realization that it was possible to peel back the layers of nature\u2019s beauty and discover, as she says, \u201chow and why things worked at the most fundamental and inner level.\u201d Life was made up of molecules<\/strong>. The chemical components and structure of these molecules governed what they would do.<\/p><\/blockquote>\n\n\n\n
\u751f\u547d\u662f\u5206\u5b50\u6784\u6210\u7684\u3002<\/p>\n\n\n\n
The key aspect of his intellect, she realized, was his ability to make unexpected connections between different fields<\/strong>. More than four thousand disease-causing DNA mutations were found. But no cure sprang forth for even the most simple of single-gene disorders, such as Tay-Sachs, sickle cell, or Huntington\u2019s.<\/p><\/blockquote>\n\n\n\n
\u79d1\u5b66\u53d1\u73b0\u7684\u6838\u5fc3\u80fd\u529b\u662f\u4e0d\u540c\u9886\u57df\u4e4b\u95f4\u5efa\u7acb\u770b\u4f3c\u4e0d\u5b58\u5728\u7684\u94fe\u63a5\u3002DNA\u7a81\u53d8\u5df2\u7ecf\u5e26\u6765\u4e864000\u79cd\u75be\u75c5\u3002<\/p>\n\n\n\n
As a young PhD student, Doudna mastered the special combination of skills that distinguished Szostak and other great scientists: she was good at doing hands-on experiments <\/strong>and also at asking the big questions<\/strong>. She knew that God was in the details but also in the big picture<\/strong>. Jennifer was fantastically good at the bench, because she was fast and sharp and could seemingly get anything to work,\u201d Szostak says. \u201cBut we talked quite a bit about why the really big questions are the important questions.<\/p><\/blockquote>\n\n\n\n
\u4e0a\u5e1d\u5728\u7ec6\u8282\u4e2d\uff0c\u4e5f\u5728\u5927\u7684\u56fe\u666f\u4e2d\u3002<\/p>\n\n\n\n
Many viruses are composed of DNA, but SARS was a coronavirus that instead contained RNA. By the time it died out after eighteen months, it had killed close to eight hundred people around the world. It was officially known as SARS-CoV. In 2020, it had to be renamed SARS-CoV-1.<\/p><\/blockquote>\n\n\n\n
\u8bb8\u591a\u75c5\u6bd2\u662fDNA\u7684\uff0cSARS\u662fRNA\u75c5\u6bd2\u3002<\/p>\n\n\n\n
RNA interference operates by deploying an enzyme known as \u201cDicer.\u201d Dicer snips a long piece of RNA into short fragments. These little fragments can then embark on a search-and-destroy mission: they seek out a messenger RNA molecule that has matching letters, then they use a scissors-like enzyme to chop it up. The genetic information carried by that messenger RNA is thus silenced.\u201d<\/p>
Mojica was driving home from his lab one evening when he came up with the name CRISPR, for \u201cclustered regularly interspaced short palindromic repeats.\u201d<\/p><\/blockquote>\n\n\n\n
RNA\u5e72\u6270\u3002<\/p>\n\n\n\n
Indeed, phage viruses are by far the most plentiful biological entity on earth. There are 10^31 of them\u2014a trillion phages for every grain of sand, and more than all organisms (including bacteria) combined. In one milliliter (0.03 ounces) of seawater there can be as many as 900 million of these viruses.<\/p><\/blockquote>\n\n\n\n
\u817a\u75c5\u6bd2\u5e7f\u6cdb\u5b58\u5728\uff0c1g\u6ce5\u571f\u91cc\u670910^31\u4e2a\u30021\u6beb\u5347\u6d77\u6c34\u80fd\u88c5\u4e0b9\u4ebf\u4e2a\u75c5\u6bd2\u3002<\/p>\n\n\n\n
It was an astonishing and elegant discovery, one that would have great repercussions. But Mojica had a ridiculously difficult time getting it published. He submitted a paper to Nature in October 2003 entitled \u201cProkaryotic Repeats Are Involved in an Immunity System.\u201d In other words, CRISPR systems were a way that bacteria acquired immunity to viruses. <\/p><\/blockquote>\n\n\n\n
CRISPR\u7cfb\u7edf\u662f\u7ec6\u83cc\u5bf9\u75c5\u6bd2\u7684\u514d\u75ab\u7cfb\u7edf\u3002<\/p>\n\n\n\n
In Conti\u2019s lab, Jinek developed a passion for the star molecule of this book, RNA. \u201cIt\u2019s such a versatile molecule\u2014it can do catalysis, it can fold into 3D structures,\u201d he later told Kevin Davies of the CRISPR Journal. \u201cAt the same time, it\u2019s a carrier of information. It\u2019s an all-rounder in the world of biomolecules!\u201dHis goal was to work in a lab where he could figure out the structure of complexes that combined RNA and enzymes.<\/p><\/blockquote>\n\n\n\n
CRISPR\u7684\u795e\u5947\u4e4b\u5904\uff0c\u53ef\u4ee5\u5f53\u50ac\u5316\u5242\uff0c\u8fd8\u53ef\u4ee5\u6298\u53e0\u51fa3D\u7ed3\u6784\uff0c\u8fd8\u53ef\u4ee5\u643a\u5e26\u4fe1\u606f\u3002<\/p>\n\n\n\n
In other words, CRISPR did not work through RNA interference, which had been the general consensus when Banfield first approached Doudna. Instead, the CRISPR system targeted the DNA of the invading virus. That had a holy-cow implication.<\/p>
However, as with the transistor, it was not simply a one-way linear progression. Instead, there was an iterative dance among basic scientists, practical inventors, and business leaders. Science can be the parent of invention. But as Matt Ridley points out in his book How Innovation Works, sometimes it\u2019s a two-way street. \u201cIt is just as often the case that invention is the parent of science: techniques and processes are developed that work, but the understanding of them comes later,<\/strong>\u201d he writes. \u201cSteam engines led to the understanding of thermodynamics, not the other way round. Powered flight preceded almost all aerodynamics.\u201d<\/p><\/blockquote>\n\n\n\n
\u53d1\u660e\u662f\u79d1\u5b66\u4e4b\u6bcd\u3002\u5148\u662f\u6280\u672f\u53d1\u5c55\u628a\u4e8b\u60c5\u505a\u51fa\u6765\uff0c\u662f\u540e\u9762\u518d\u53bb\u7406\u89e3\u548c\u89e3\u91ca\u3002<\/p>\n\n\n\n
But a different approach was required in order to determine the essential components of the system: biochemists working with the molecules in vitro, in a test tube. By isolating the components in a test tube, biochemists could explain at the molecular level the discoveries made by microbiologists working in vivo and by computational geneticists comparing sequencing data in silico.<\/p>
It began making genetically engineered drugs and, in August 1978, blasted into hypergrowth when it won a bet-the-company race to make a synthetic version of insulin to treat diabetes.Until then, one pound of insulin required eight thousand pounds of pancreas glands ripped from more than twenty-three thousand pigs or cows.<\/p><\/blockquote>\n\n\n\n
\u80f0\u5c9b\u7d20\u524d\u671f\u7684\u6545\u4e8b\uff0c2\u78c5\u7684\u52a8\u7269\u63d0\u53d6\u8981\u4ece8000\u78c5\u80f0\u817a\u4e2d\u63d0\u53d6\uff0c\u9700\u898123000\u53ea\u732a\u6216\u8005\u725b\u3002<\/p>\n\n\n\n
She was forty-four, happily married, with a smart and polite seven-year-old son. Yet despite all of her success, or maybe partly because of it, she was having a mild midlife crisis<\/strong>. \u201cI\u2019d been running an academic research lab for fifteen years, and I started to wonder, \u2018Is there more?\u2019\u200a\u201d she recalls. \u201cI wondered if my work was having an impact in the broader sense.\u201d<\/p><\/blockquote>\n\n\n\n
\u79d1\u5b66\u5bb6\u4e5f\u4f1a\u6709\u4e2d\u5e74\u5371\u673a\uff0c44\u5c81\u7684Jennifer+7\u5c81\u513f\u5b50\u3002<\/p>\n\n\n\n
Swanson had an unbroken record of failure<\/strong> as a venture capitalist. At the time, he was living in a shared apartment<\/strong>, driving a beat-up Datsun, and surviving on cold-cut sandwiches<\/strong>. But he had read up on recombinant DNA and convinced himself that he had finally found a winning horse.<\/p><\/blockquote>\n\n\n\n
\u57fa\u56e0\u6cf0\u514b\u521b\u59cb\u4eba\u5f53\u5e74\u7684\u7a98\u5883\uff1a\u6295\u8d44\u5de5\u4f5c\u906d\u9047\u8fde\u7eed\u5931\u8d25\u3001\u5408\u79df\u3001\u5403\u51b7\u9762\u5305\u6df7\u65e5\u5b50\u3002<\/p>\n\n\n\n
There are two components to scientific discovery: doing great research and building a lab that does great research. I once asked Steve Jobs what his best product was, thinking he would say the Macintosh or iPhone. Instead he said that creating great products is important, but what\u2019s even more important is creating a team that can continually make such products<\/strong>.<\/p><\/blockquote>\n\n\n\n
\u79d1\u5b66\u53d1\u73b0\u7684\u4e24\u4e2a\u90e8\u5206\uff1a\u505a\u597d\u7814\u7a76\u548c\u5efa\u4e00\u4e2a\u80fd\u505a\u597d\u7814\u7a76\u7684\u5b9e\u9a8c\u5ba4\u56e2\u961f\uff0c\u597d\u56e2\u961f\/\u597d\u516c\u53f8\u8981\u66f4\u91cd\u8981\u3002<\/p>\n\n\n\n
They had also established the essential role of another part of the complex: CRISPR RNAs, known as crRNAs. These are the small snippets of RNA that contain some genetic coding from a virus that had attacked the bacteria in the past. This crRNA guides the Cas enzymes to attack that virus when it tries to invade again. These two elements are the core of the CRISPR system: a small snippet of RNA that acts as a guide and an enzyme that acts as scissors.<\/p>
It turns out that tracrRNA performs two important tasks. First, it facilitates the making of the crRNA, the sequence that carries the memory of a virus that previously attacked the bacteria. Then it serves as a handle to latch on to the invading virus so that the crRNA can target the right spot for the Cas9 enzyme to chop.<\/p><\/blockquote>\n\n\n\n
crRNA<\/p>\n\n\n\n
There were lessons from the arts, she would discover, that applied to science. \u201cMethodology is important in both,\u201d she says. \u201cYou also must know the basics<\/strong> and master the methods<\/strong>. That requires persistence\u2014repeating experiments and repeating them again, perfecting how to prepare the DNA when you clone a gene, and then doing it over and over again. It\u2019s part of the training, just like the hard work of a ballet dancer, repeating all day long the same moves and methods.<\/p><\/blockquote>\n\n\n\n
\u4e86\u89e3\u57fa\u7840\u5e38\u8bc6+\u638c\u63e1\u65b9\u6cd5\u8bba\uff0c\u4e0d\u6b62\u827a\u672f\u548c\u751f\u7269\u5982\u6b64\uff0c\u6295\u8d44\u4e5f\u5982\u6b64\u3002<\/p>\n\n\n\n
\u201cI enjoy the freedom of being on my own, of not depending on partnership,\u201d she says. She hated the phrase \u201cwork-life balance\u201d because it implied that work competes with life<\/strong>. Her work in the lab and her \u201cpassion for science,\u201d she says, brought her a \u201chappiness that is as fulfilling as any other passion.<\/p><\/blockquote>\n\n\n\n
\u5de5\u4f5c\u751f\u6d3b\u4e0d\u4e00\u5b9a\u8981\u51b2\u7a81\u3002<\/p>\n\n\n\n
It worked: the three-component complex reliably chomped up the target DNA. Jinek immediately told Doudna the news: \u201cWithout the tracrRNA, the crRNA guide does not bind to the Cas9 enzyme.\u201d After that breakthrough, Doudna and Charpentier became more involved in the daily work. Clearly they were heading to an important discovery: determining the essential components of a CRISPR gene-cutting system.<\/p>
\u201cWe found this protein, an enzyme called Cas9,\u201d she explained. \u201cIt can be programmed to find viruses and cut them up. It\u2019s so incredible.\u201d<\/p>
It was immediately obvious that this single guide would make CRISPR-Cas9 an even more versatile, easy-to-use, and reprogrammable tool for gene editing. What made the single-guide system particularly significant\u2014from both a scientific and an intellectual property standpoint\u2014was that it was an actual human-made invention, not merely a discovery of a natural phenomenon.<\/p>
The 3,500-word paper went into great detail on how the crRNA and the tracrRNA worked to bind the Cas9 protein onto the target DNA. It also showed how the structure of two Cas9 domains determined how each cut one of the DNA strands at a specific location. Finally, it described how they were able to fuse the crRNA and tracrRNA to engineer a single-guide RNA. This system, the authors noted, could be used to edit genes.<\/p><\/blockquote>\n\n\n\n
CRISPR\u7684\u5173\u952e\u70b9\u3002<\/p>\n\n\n\n
Researchers were able to devise proteins that could serve as a guide to get the cutting domain to a targeted DNA sequence. One system, zinc-finger nucleases (ZFNs), came from fusing the cutting domain with a protein that has little fingers shaped by the presence of a zinc ion, which allow it to grasp on to a specified DNA sequence. A similar but even more reliable method, known as TALENs (transcription activator\u2013like effector nucleases), came from fusing the cutting domain with a protein that could guide it to longer DNA sequences.\u201d<\/p>
\u201cWith ZFNs and TALENs, you had to construct a new protein guide every time you wanted to target a different genetic sequence to cut; it was difficult and time consuming. But with CRISPR you merely had to fiddle with the genetic sequence of the RNA guide. A good student could do it quickly in a lab.\u201d<\/p>
\u201cIn the Saturday enrichment class, the focus was on DNA and how RNA carried out its instructions, with an emphasis on the role played in this process by enzymes, those protein molecules that act as catalysts to spark actions in a cell. \u201cMy teacher loved enzymes,\u201d Zhang says. \u201cHe told me that whenever you face a tough question in biology, just say \u2018Enzymes.\u2019 It\u2019s the correct answer to most questions in biology.\u201d<\/p>
\u201cIn addition, he used a well-known technique called \u201ccodon optimization\u201d to make the CRISPR-Cas9 system work in human cells. Codons are the three-letter snippets of DNA that provide instructions for the specific arrangement of amino acids, which are the building blocks used to make proteins. A variety of codons can code for the same amino acid. In different organisms, one or another of these alternative codons may work more efficiently. When trying to move a gene-expression system from one organism to another, such as from bacteria to a human, codon optimization switches the codon sequence to the one that works best.\u201d<\/p>
\u201cIn September 2013, Gengine, Inc. was founded. Two months later, it changed its name to Editas Medicine. \u201cWe have the ability to essentially target any gene,\u201d said Kevin Bitterman, a principal at Polaris Partners who served as the interim president for the first few months. \u201cAnd we have in our crosshairs any diseases with a genetic component. We can go in and fix the error.\u201d<\/p>
\u201cOn April 15, 2014, she received an email from a reporter asking for her reaction to the news that Zhang and the Broad had just been granted a patent for the use of CRISPR-Cas9 as an editing tool. Doudna and Charpentier still had a patent application pending, but Zhang and the Broad, who had put in their own application later, had paid to have their decision fast-tracked. Suddenly it became clear, to Doudna at least, that Zhang and Lander were trying to relegate her and Charpentier to minor players\u2014both in history and in any commercial use of CRISPR-Cas9.\u201d<\/p>
\u201cWithin a few months, she decided that she would be most comfortable working with her trusted partner and former student Rachel Haurwitz, with whom she had started Caribou Biosciences in 2011. Caribou had created a spinoff called Intellia, with the mission of commercializing CRISPR-Cas9 tools. \u201cI became very interested in Intellia, because the Caribou team was launching it with the academic scientists I most liked and trusted and respected,\u201d Doudna says. \u00a0<\/p>
As a result, the pioneers of CRISPR-Cas9 ended up in three competing companies: CRISPR Therapeutics, founded by Charpentier and Novak; Editas Medicine, which included Zhang and Church and Doudna until she resigned; and Intellia Therapeutics, founded by Doudna, Barrangou, Sontheimer, Marraffini, and Haurwitz.\u201d<\/p>
\u201cAs a result, other patent applications were deemed to have an earlier priority date, and the court revoked Zhang\u2019s patent. \u201cFeng\u2019s European patent was nullified because of the way he took me off,\u201d Marraffini says.28 By 2020, Doudna and Charpentier had been awarded the major patents also in Britain, China, Japan, Australia, New Zealand, and Mexico.\u201d<\/p>
\u201cTo an unnecessary extent, the prolonged fight was driven by emotions and resentments. Instead, Doudna and Zhang could have followed the example of Jack Kilby of Texas Instruments and Robert Noyce of Intel who, after five years of wrangling, agreed to share the patent rights for the microchip by cross-licensing their intellectual property to each other and splitting the royalties, which helped the microchip business grow exponentially and define a new age of technology. Unlike the CRISPR contestants, Noyce and Kilby obeyed an all-important business maxim: Don\u2019t fight over divvying up the proceeds until you finish robbing the stagecoach.<\/p>
\u201cThe primary scientific goal of the initiative is to find a method to edit the sickle-cell mutation inside of a patient without needing to extract bone marrow. One possibility is to inject into the patient\u2019s blood a gene-editing molecule with an address label that directs it right to the cells in the bone marrow. The difficult part will be to find the right delivery mechanism, such as a virus-like particle, that won\u2019t trigger the patient\u2019s immune system.\u201d<\/p>
Cancer: In addition to treating blood disorders, such as sickle-cell anemia, CRISPR has been used to fight cancer. China has been the pioneer in this field, and it is two or three years ahead of the United States in devising treatments and getting them into clinical trials. The first person to be treated was a lung-cancer patient in Chengdu, a city of 14 million in the western Chinese province of Sichuan. In October 2016, a team removed from the patient\u2019s blood some of his T-cells, which are the white blood cells that help fight off diseases and confer immunity. The doctors then used CRISPR-Cas9 to disable a gene that produces a protein, known as PD-1, which stops the cell\u2019s immune response. Cancer cells sometimes trigger the PD-1 response, thus protecting themselves from the immune system. By using CRISPR to edit the gene, the patient\u2019s T-cells become more effective in killing the cancer cells. Within a year, China had seven clinical trials using this technique.\u201d<\/p>
\u201cDoudna assigned the project to two young postdoctoral students who had just joined her lab, Kyle Watters and Gavin Knott. They focused on a method that some viruses use to disable the CRISPR systems of the bacteria they are attacking. In other words, bacteria developed CRISPR systems to ward off viruses, but then the viruses developed a way to shut down those defenses. It was an arms race the Pentagon could understand: missiles being countered by defense systems being countered by anti\u2013defense systems. The newly discovered systems were dubbed \u201canti-CRISPRs.\u201d<\/p>
\u201cOne of the primary organizers was a soft-spoken but gently commanding MIT biology professor named David Baltimore, who that year would win the Nobel Prize for his work showing that viruses containing RNA, such as coronaviruses, can insert their genetic material into the DNA of a host cell through a process known as \u201creverse transcription.\u201d In other words, the RNA can be transcribed into DNA, thus modifying the central dogma of biology, which states that genetic information travels in only one direction, from DNA to RNA. \u201d<\/p>
\u201cStock went on to write a pro-editing manifesto, Redesigning Humans: Our Inevitable Genetic Future. \u201cA key aspect of human nature is our ability to manipulate the world,\u201d he argued. \u201cTo turn away from germline selection and modification without even exploring them would be to deny our essential nature and perhaps our destiny.\u201d<\/p>
\u201cUnlike some other scientists at the time,8 the participants had purposely decided against calling for a ban or moratorium, which can over time become hard to lift. Their goal was to keep open the possibility of germline editing if it was safe and medically necessary. That was why, in the title of the piece, they called for \u201ca prudent path forward,\u201d which had become the watchword of many of the scientific conferences \u201d<\/p>
\u201cOver the next six years, Jiankui\u2019s company would receive about $5.7 million in funding from government sources. By 2017, its gene sequencer was on the market and the company, of which Jiankui had a one-third stake, was valued at $313 million. \u201cWe confirmed Nana\u2019s CCR5 gene was edited successfully with frameshift mutations on both alleles and Lulu\u2019s was heterozygous,\u201d he admitted. In other words, Lulu had different gene versions on her two chromosomes, which meant that her system would still produce some of the CCR5 protein.\u201d<\/p>
\u201cSomatic editing can be used on certain types of cells, such as those of the blood, muscles, and eyes. But it is expensive, doesn\u2019t work on all cells, and may not be permanent. Germline edits could make a fix in all of the cells of the body. Thus it holds a lot more promise. And a lot more perceived peril.\u201d<\/p>
\u201cMemory may be the first mental improvement we will be able to engineer, and fortunately it is a less fraught topic than IQ. It has already been improved in mice, such as by enhancing the genes for NMDA receptors in nerve cells. In humans, enhancing those genes could help prevent memory loss in old age, but it could also enhance memory in younger people as well\u201d<\/p>
\u201cThe role of sports, at least since the first Olympics in 776 BC, is to celebrate two things: natural talent combined with disciplined effort. Enhancements would shift that balance, making human effort less of a component of victory. Therefore the achievement becomes a little less praiseworthy and inspiring. There is a whiff of cheating if an athlete succeeds by obtaining some physical advantages through medical engineering.\u201d<\/p>
\u201cLikewise, suppose I\u2019m an average height. If I were enhanced by eight inches, I\u2019d be way taller than most people, and that could be a benefit to me. But if everyone else got the same eight-inch enhancement I did, then I would get no real benefit. The enhancement wouldn\u2019t make me or society as a whole better off, especially given the legroom of airline seats these days. The only sure beneficiaries would be carpenters who specialized in raising door frames. So enhanced height is a positional good, while enhanced resistance to viruses is an absolute good\u201d<\/p>
\u201cAt this point in our deliberations, we have to face the potential conflict between what is desired by the individual versus what is good for human civilization. A reduction in mood disorders would be seen as a benefit by most of the afflicted individuals, parents, and families. They would desire it. \u201d<\/p>
\u201cIn the meantime, we will have to deploy the finite allocation of wisdom that nature has dealt us as we ponder how to use the gene-editing techniques that we\u2019ve discovered. Ingenuity without wisdom is dangerous.\u201d<\/p>
\u201cOur respect for nature and nature\u2019s God should, indeed, instill some humility about meddling with our genes. But should it absolutely forbid it? After all, we Homo sapiens are part of nature, no less so than bacteria and sharks and butterflies. Through its infinite wisdom or blind stumbling, nature has endowed our species with an ability to edit our own genes. If it\u2019s wrong for us to use CRISPR, the reason cannot merely be that it\u2019s unnatural. It\u2019s just as natural as all of the tricks that bacteria and viruses use.\u201d<\/p>
It didn\u2019t happen. When the real 1984 actually rolled around, Apple introduced an easy-to-use personal computer, the Macintosh, and in the words that Steve Jobs wrote for its ad, \u201cyou\u2019ll see why 1984 won\u2019t be like 1984.\u201d That phrase contained a deep truth. Instead of computers becoming an instrument for centralized repression, the combination of the personal computer and the decentralized nature of the internet became a way to devolve more power down to each individual, thus unleashing a gusher of free expression and radically democratized media. Perhaps too much so. The dark side of our new information technology is not that it allows government repression of free speech but just the opposite: it permits anyone to spread, with little risk of being held accountable, any idea, conspiracy, lie, hatred, scam, or scheme, with the result that societies become less civil and governable.\u201d<\/p>
\u201cAlthough this sounds like a scene from Gattaca, a real-world version of this baby-designing service\u2014using preimplantation diagnosis\u2014was launched in 2019 by a New Jersey startup, Genomic Prediction. In vitro fertilization clinics can send the company genetic samples of prospective babies. \u201d<\/p>
For all of history, humans (and every other species) have been battling rather than accepting nature\u2019s poisoned offerings. Mother Nature has produced massive suffering and distributed it unequally. Thus we devise ways to combat plagues, cure diseases, fix disabilities, and breed better plants, animals, and children.\u201d<\/p>
\u201cEvolution\u2019s primary guide is reproductive fitness\u2014what traits might cause an organism to reproduce more\u2014which means it permits, and perhaps even encourages, all sorts of plagues, including coronaviruses and cancers, that afflict an organism once its childbearing use is over. This does not mean that, out of respect for nature, we should quit searching for ways to fight against coronaviruses and cancer.\u201d<\/p>
\u201cI am not sure how to make a sharp distinction in medicine between what is natural and what is unnatural, and I think it\u2019s dangerous to use that dichotomy to block something that could alleviate suffering and disability.\u201d<\/p>
\u201cHis nerve cells would soon start dying and eventually he would be unable to walk, speak, then swallow or eat. He was doomed to die an early and painful death. The note was a wrenching plea for help. \u201cHow could you not want to make progress on coming up with ways to prevent such a thing?\u201d Doudna asks. \u201cMy heart broke.\u201d If gene editing could prevent this in the future, it would be immoral not to pursue it, she decided.\u201d<\/p>
\u201cBy limiting gene edits to those that are truly \u201cmedically necessary,\u201d she says, we can make it less likely that parents could seek to \u201cenhance\u201d their children, which she feels is morally and socially wrong. The line between medical treatment and enhancement can be blurry, she acknowledges, but it is not totally meaningless.\u201d<\/p>
\u201cInstead of making a cut in the double-stranded DNA, the newly discovered CRISPR system would insert a new chunk of DNA by harnessing transposons, known as \u201cjumping genes,\u201d which are big segments of DNA that can hop from one place to another on chromosomes.\u201d<\/p>
\u201cThe challenge with human gene editing,\u201d she tells me, \u201cis to get your editing tools past the cell\u2019s outer plasma membrane and past its nuclear membrane to get to where the DNA is, and then you also have to get your tools to find the location in the genome.\u201d<\/p>
\u201cWhen the American Masters series on PBS decided to do a documentary on Watson in 2018, it set out to produce a balanced, intimate, complex, and nuanced look at both his scientific triumphs and his controversial views.\u201cWhat matters now are his perfections, not his past imperfections.\u201d12 Perhaps people may say that of Watson someday, but in 2019 he was an outcast.<\/p>
\u201cIn SARS-CoV-2, the RNA is about 29,900 base letters long, compared to more than three billion in human DNA. The viral sequence provides the code for making a mere twenty-nine proteins.4\u201d<\/p>
\u201cIn addition to the previously known Cas9 and Cas12 enzymes that target DNA, Zhang and Koonin found a class of enzymes that target RNA.3 They became known as Cas13.<\/p>
Cas13 had the same odd trait as Cas12: when it found its target, it went into a cutting frenzy. The Cas13 not only cut its targeted RNA, it then proceeded to cut up any other nearby RNA.\u201d<\/p>
\u201cZhang speculated that it was an evolutionary method to have the cell commit suicide if it got too infected by an invading virus, thus preventing the virus from spreading as fast.\u201d<\/p>
\u201cZhang decided to start a diagnostics company to commercialize SHERLOCK, just like Chen and Harrington had launched Mammoth. Zhang\u2019s cofounders included the two graduate students who were the lead authors on many of the papers from his lab describing CRISPR-Cas13\u201d.\u201cYou know, nature\u2019s got a ton of amazing secrets in it,\u201d he says.\u201d<\/p>
\u201cIt took a while to get Sherlock Biosciences funded and launched because Zhang and his two graduate students did not want profit to be the main goal of the company. They wanted the technologies to be affordable in the developing world. So the company was structured in a way that allowed it to profit on its innovations while still taking a nonprofit approach in places where there was great need.<\/p>
\u201cBut then, at the beginning of 2020, the world suddenly changed. The ability to quickly detect an attacking virus became critical. And the best way to do it faster and cheaper than the conventional PCR tests, which required a lot of mixing steps and temperature cycles, was to deploy RNA-guided enzymes that had been programmed to detect the genetic material of the virus\u2014in other words, adapt the CRISPR system that bacteria had been deploying for millions of years.\u201d<\/p>
\u201cThe CRISPR-based tests developed by Mammoth and Sherlock are cheaper and faster than conventional PCR tests. They also have an advantage over antigen tests, such as the one developed by Abbott Labs that was approved in August of the plague year. The CRISPR-based tests can detect the presence of the RNA of a virus as soon as a person has been infected. But the antigen tests, which detect the presence of proteins that exist on the surface of the virus, are most accurate only after a patient has become highly infectious to others.\u201d<\/p>
\u201cThe development of home testing kits has a potential impact beyond the fight against COVID: bringing biology into the home, the way that personal computers in the 1970s brought digital products and services\u2014and an awareness of microchips and software code\u2014into people\u2019s daily lives and consciousness.\u201d<\/p>
\u201cMarson and Wilson devised a way to address the DNA vaccine delivery problem using CRISPR-Cas9. They put together a Cas9 protein, a guide RNA, and a nuclear localization signal that helps the complex get into the nucleus. The result was a \u201cshuttle\u201d that could get the DNA vaccine into cells. The DNA then directs the cells to make coronavirus spike proteins and thus stimulate the immune system to fend off the real coronavirus.4 It\u2019s a brilliant idea that could have uses for many treatments in the future, but it has been difficult to make work. By the beginning of 2021, Wilson and Marson were still trying to prove it could be effective.\u201d<\/p>
\u201cAn RNA vaccine has certain advantages over a DNA vaccine. Most notably, the RNA does not need to get into the nucleus of the cell, where DNA is headquartered. The RNA does its work in the outer region of cells, the cytoplasm, which is where proteins are constructed. So an RNA vaccine simply needs to deliver its payload into this outer region.\u201d<\/p>
\u201cAfeyan instantly authorized him to start work without waiting for full board approval. Lacking Pfizer\u2019s resources, Moderna had to depend on funding from the U.S. government. Anthony Fauci, the government\u2019s infectious disease expert, was supportive. \u201cGo for it,\u201d he declared. \u201cWhatever it costs, don\u2019t worry about it.\u201d It took Moderna only two days to create the desired RNA sequences that would produce the spike protein, and thirty-eight days later it shipped the first box of vials to the NIH to begin early-stage trials. Afeyan keeps a picture of that box on his cell phone.<\/p>
\u201cThe invention of easily reprogrammable RNA vaccines was a lightning-fast triumph of human ingenuity, but it was based on decades of curiosity-driven research into one of the most fundamental aspects of life on planet earth: how genes encoded by DNA are transcribed into snippets of RNA that tell cells what proteins to assemble. Likewise, CRISPR gene-editing technology came from understanding the way that bacteria use snippets of RNA to guide enzymes to chop up dangerous viruses. Great inventions come from understanding basic science. Nature is beautiful that way.\u201d<\/p>
\u201cThe result was a burst of papers in the spring of 2020 for improving CRISPR-based detection technologies for viruses. These included a system known as CARMEN, designed to detect 169 viruses at one time,11 and a process that combined SHERLOCK\u2019s detection capability with an RNA extraction method called HUDSON to create a single-step detection technique he named SHINE.12 In addition to its CRISPR wizardry, the Broad was a master at devising acronyms.\u201d<\/p>
\u201cOne of the transformations wrought by the coronavirus pandemic is that more meetings in the future will be done virtually. It\u2019s a shame. If COVID doesn\u2019t kill us, Zoom will. As Steve Jobs emphasized when he built a headquarters for Pixar and planned a new Apple campus, new ideas are born out of serendipitous encounters. In-person interactions are especially important in the initial brainstorming of new ideas and the forging of personal bonds. As Aristotle taught, we are a social animal, an instinct that cannot fully be satisfied online.\u201d<\/p>
\u201cThe awarding of the 2020 Nobel Prize in Chemistry to Doudna and Charpentier was not a complete surprise, but the recognition came with historic swiftness. Their CRISPR discovery was merely eight years old. The day before, Sir Roger Penrose had shared the Nobel in physics for a discovery about black holes he had made more than fifty years earlier.\u201d<\/p>
\u201cAll of the scientists I write about in this book say that their main motivation is not money, or even glory, but the chance to unlock the mysteries of nature and use those discoveries to make the world a better place. I believe them. And I think that may be one of the most important legacies of the pandemic: reminding scientists of the nobility of their mission.\u201d<\/p>
\u201cAfter millions of centuries during which the evolution of organisms happened \u201cnaturally,\u201d we humans now have the ability to hack the code of life and engineer our own genetic future. Or, to flummox those who would label gene editing as \u201cunnatural\u201d and \u201cplaying God,\u201d let\u2019s put it another way: Nature and nature\u2019s God, in their infinite wisdom, have evolved a species that is able to modify its own genome, and that species happens to be ours.<\/p>
Like any evolutionary trait, this new ability may help the species thrive and perhaps even produce successor species. Or it may not. It could be one of those evolutionary traits that, as sometimes happens, leads a species down a path that endangers its survival. Evolution is fickle that way.\u201d<\/p><\/blockquote>\n\n\n\n
<\/p>\n","protected":false},"excerpt":{"rendered":"
\u4e00\u672c\u8bb2\u57fa\u56e0\u7f16\u8f91\u6280\u672f\u53d1\u660e\u4ebaDoudna Jennifer\u548c\u5176\u7ade\u4e89\u8005\u5f20\u5cf0\u7684\u6545\u4e8b\u3002\u57fa\u56e0\u7f16\u8f91\u7684\u53d1\u73b0\u5386\u53f2\u4e0d\u8fc7\u624d\u5341\u5e74\u7684\u65f6\u95f4 […]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[5],"tags":[],"class_list":["post-1264","post","type-post","status-publish","format-standard","hentry","category-book"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/p6VzCl-ko","jetpack-related-posts":[{"id":856,"url":"https:\/\/www.yizhayan.org\/wp\/?p=856","url_meta":{"origin":1264,"position":0},"title":"\u300a\u6280\u672f\u7684\u672c\u8d28\u300b1905","author":"yizhayanorg@126.com","date":"2019 \u5e74 5 \u6708 1 \u65e5","format":false,"excerpt":"\u672c\u6765\u611f\u89c9\u633a\u67af\u71e5\u7684\u4e66\uff0c\u8d8a\u8bfb\u8d8a\u53d1\u73b0\u6709\u610f\u601d\u3002\u4e8e\u662f\u5728Ipad\u4e0a\u8bfb\u4e86\u4e00\u904d\uff0c\u53c8\u4e70\u4e86\u672c\u7eb8\u8d28\u4e66\u8ba1\u5212\u5b58\u8d77\u6765\uff0c\u6709\u65f6\u95f4\u518d\u8bfb\u2026","rel":"","context":"\u5728\u201cBook\u201d\u4e2d","block_context":{"text":"Book","link":"https:\/\/www.yizhayan.org\/wp\/?cat=5"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":1776,"url":"https:\/\/www.yizhayan.org\/wp\/?p=1776","url_meta":{"origin":1264,"position":1},"title":"\u6280\u672f\u4e0e\u6587\u660e 2516","author":"yizhayanorg@126.com","date":"2025 \u5e74 12 \u6708 14 \u65e5","format":false,"excerpt":"\u542c\u64ad\u5ba2\u7684\u65f6\u5019\u542c\u5230\u4e86\u5f20\u7b11\u5b87\u7684\u8fd9\u5957\u4e66\uff0c\u6587\u660e\u53f2\u662f\u5f88\u96be\u5199\u7684\uff0c\u8fd9\u5957\u4e66\u7684\u9898\u76ee\u672c\u8eab\u5f88\u96be\uff0c\u6240\u4ee5\u8bfb\u8d77\u6765\u548c\u6211\u9884\u671f\u7684\u6709\u4e00\u5b9a\u2026","rel":"","context":"\u5728\u201cBook\u201d\u4e2d","block_context":{"text":"Book","link":"https:\/\/www.yizhayan.org\/wp\/?cat=5"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":1342,"url":"https:\/\/www.yizhayan.org\/wp\/?p=1342","url_meta":{"origin":1264,"position":2},"title":"\u300a\u7406\u6027\u4e50\u89c2\u6d3e\u300b2239","author":"yizhayanorg@126.com","date":"2022 \u5e74 12 \u6708 25 \u65e5","format":false,"excerpt":"\u5e74\u672b\u6536\u5c3e\u8865\u7b14\u8bb0\u7684\u4e66\u3002\u9053\u7406\u57fa\u672c\u90fd\u5728\u4e66\u540d\u91cc\u4e86\uff0c\u8bfb\u8d77\u6765\u6bd4\u8f83\u8f7b\u677e\uff0c\u9009\u62e9\u82e5\u5e72\u5386\u53f2\u65e0\u975e\u662f\u63cf\u8ff0\u8fd9\u4ef6\u4e8b\uff0c\u786e\u5b9e\u4e50\u89c2\u662f\u4eba\u2026","rel":"","context":"\u5728\u201cBook\u201d\u4e2d","block_context":{"text":"Book","link":"https:\/\/www.yizhayan.org\/wp\/?cat=5"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":1378,"url":"https:\/\/www.yizhayan.org\/wp\/?p=1378","url_meta":{"origin":1264,"position":3},"title":"\u300a\u730e\u836f\u5e08\u300b2307","author":"yizhayanorg@126.com","date":"2023 \u5e74 1 \u6708 28 \u65e5","format":false,"excerpt":"\u4e70\u4e86\u5feb\u4e00\u5e74\u4e86\u3002\u76f4\u5230\u4eca\u5e74\u6625\u8282\u671f\u95f4\u53bb\u5e7f\u5143\u7684\u822a\u73ed\u4e0a\u624d\u8bfb\u5b8c\u7684\u4e00\u672c\u5173\u4e8e\u65b0\u836f\u53d1\u73b0\u7684\u4e66\uff0c\u4f5c\u8005\u662f\u836f\u7269\u7814\u53d1\u4eba\u5458\u51fa\u8eab\uff0c\u5199\u2026","rel":"","context":"\u5728\u201cBook\u201d\u4e2d","block_context":{"text":"Book","link":"https:\/\/www.yizhayan.org\/wp\/?cat=5"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":813,"url":"https:\/\/www.yizhayan.org\/wp\/?p=813","url_meta":{"origin":1264,"position":4},"title":"\u300a\u9a71\u52a8\u4e16\u754c\u7684100\u9879\u6280\u672f\u300b1803","author":"yizhayanorg@126.com","date":"2018 \u5e74 10 \u6708 23 \u65e5","format":false,"excerpt":"\u7b80\u8981\u8282\u9009 \u5236\u9020 \u65e0\u57fa\u677f\u7ec4\u88c5 \u57fa\u7840\u8bbe\u65bd\u673a\u5668\u4eba \u751f\u7269\u81ea\u4fee\u590d\u7684\u6df7\u51dd\u571f\u6750\u6599\/\u82bd\u5b62\u6746\u83cc \u534f\u4f5c\u673a\u5668\u4eba-\u5409\u91ce\u5bb6cp\u2026","rel":"","context":"\u5728\u201cBook\u201d\u4e2d","block_context":{"text":"Book","link":"https:\/\/www.yizhayan.org\/wp\/?cat=5"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":859,"url":"https:\/\/www.yizhayan.org\/wp\/?p=859","url_meta":{"origin":1264,"position":5},"title":"\u300a\u5168\u7403\u79d1\u6280\u901a\u53f2\u300b1906","author":"yizhayanorg@126.com","date":"2019 \u5e74 6 \u6708 30 \u65e5","format":false,"excerpt":"\u5434\u519b\u8001\u5e08\u7684\u6587\u5b57\u5f88\u7ec6\u817b\uff0c\u7ed3\u8bba\u4e5f\u5f88\u6709\u610f\u4e49\u3002\u5c31\u50cf\u5c01\u9762\u4e0a\u526f\u6807\u9898\u8bf4\u7684\u90a3\u6837\uff1a\u5386\u53f2\u603b\u5728\u91cd\u6f14\uff0c\u79d1\u6280\u6c38\u8fdc\u5411\u524d\u3002\u8fd9\u5c31\u662f\u8fd9\u2026","rel":"","context":"\u5728\u201cBook\u201d\u4e2d","block_context":{"text":"Book","link":"https:\/\/www.yizhayan.org\/wp\/?cat=5"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]}],"_links":{"self":[{"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=\/wp\/v2\/posts\/1264","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1264"}],"version-history":[{"count":2,"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=\/wp\/v2\/posts\/1264\/revisions"}],"predecessor-version":[{"id":1267,"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=\/wp\/v2\/posts\/1264\/revisions\/1267"}],"wp:attachment":[{"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1264"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1264"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.yizhayan.org\/wp\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1264"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}