Surprise Outbreak of Common Sense in Washington DC

News today that the Justice Department has filed an amicus brief outlining a new position that naturally occurring genes should not be patentable.  The New York Times is reporting that "while the government took the plaintiffs' side on the issue of isolated DNA, it sided with Myriad on patentability of manipulated DNA."  The change in position was evidently prompted by the decision of a federal judge this past spring that certain claims in what are known as the BRCA 1/2 patents should be overturned because those genes are preexisting in nature.  Perhaps Jon Stewart has more influence in DC than we all thought.

I am largely on board with the line taken by the Justice Department.  It is pretty close to my own analysis, as described in my post from last spring: "Big Gene Patent (Busting) News???"  There are, however, a few bits that I am still chewing on, which I will get to later.

First, in broad strokes, the government's brief supports the decision of District Judge Robert Sweet that naturally occurring gene sequences are not patentable, but weighed in against Judge Sweet's analysis that DNA coding for natural genes is not patentable if it has been restructured in an artificial construct but is still the same sequence as occurs in nature.  The most obvious example of the latter is a coding sequence with all introns removed and packed in a plasmid as a cDNA.

Here is the Justice Department's language (the text of the brief is available via the NYT page):

The district court erroneously cast doubt on the patent-eligibility of a broad range of man-made compositions of matter whose value derives from the information-encoding capacity of DNA. Such compositions -- e.g., cDNAs, vectors, recombinant plasmids, and chimeric proteins, as well as countless industrial products, such as vaccines and genetically modified crops, created with the aid of such molecules -- are in every meaningful sense the fruits of human ingenuity and thus qualify as "'human-made inventions'" eligible for patent protection under section 101. (p.9)

...The district court correctly held, however, that genomic DNA that has merely been isolated from the human body, without further alteration or manipulation, is not patent-eligible. (p.10)

...Indeed, the relationship between a naturally occurring nucleotide sequence and the molecule it expresses in a human cell -- that is, the relationship between genotype and phenotype -- is simply a law of nature. (p.10)

Here is the meat:

The chemical structure of native human genes is a product of nature, and it is no less a product of nature when that structure is "isolated" from its natural environment than are cotton fibers that have been separated from cotton seeds or coal that has been extracted from the earth.

The scope of Section 101 is purposefully wide and its threshold is not difficult to cross.  See Bilski, 130 S.Ct. at 3225.  New and useful methods of identifying, isolating, extracting, or using genes and genetic information may be patented (subject to the prohibition against patenting abstract ideas), as may nearly any man-made transformation or manipulation of the raw materials of the genome, such as cDNAs. Thus, the patent laws embrace gene replacement therapies, engineered biologic drugs, methods of modifying the properties of plants or generating biofuels, and similar advanced applications of biotechnology. Crossing the threshold of section 101, however, requires something more than identifying and isolating what has always existed in nature, no matter how difficult or useful that discovery may be. (p.11)

It might seem that the Justice Department gives back a lot of power to those who hold patents on natural genes by including cDNAs (with introns removed) as patentable material.  This would seem to give patent holders a lock on the human proteins those genes encode, because the most common way to make a protein is to use a cDNA (or similar) to express a protein in a host like E. coli or yeast.  So unless people come up with a good way to cause overexpression of human proteins from native genes via mechanisms that chop out the introns -- and some methods like that do exist -- the patent seems to block use of the protein.

But I am not sure that this brief gives any succor to those hoping for patent protection of a genetic diagnostic.  Those diagnostics generally work by using a short sequence of the gene in question as a PCR primer to find (or exclude) particular sequences of clinical interest in a patient's genome.  Those primers generally can be found in regions of DNA not interrupted by an intron, or can include the intron in the primer sequence, which means that the primer can consist of sequences that were preexisting in nature.  Only if the primer has to be composed of a sequence that -- in nature -- is interrupted by an intron but is only found in somebody's edited cDNA library without that intron would a patent protect the diagnostic assay.

A penultimate thought on the brief: I am still pondering whether the Justice Department lawyers, in their extended discussion of DNA as information carrying medium, got their analysis right.  I will have to read the brief again.  And perhaps again after that.

Finally, the brief leaves most of my previous conclusions intact, namely that the biggest impact of Judge Sweet's ruling that natural sequences cannot be patented may be for work in organisms other than humans.  From my post last May:

...the rest of the biotech industry shouldn't be concerned about thisruling, frankly.  They might even celebrate the fact that they now have access, potentially, to a whole bunch more genes that are naturally occurring.  Not just in humans, mind you, but any organism.  This opens up a rather substantial toolbox for anybody interested in using biological technologies derived from viruses, bacteria, plants, etc.  If it holds up over the long run, Judge Sweet's decision should accelerate innovation.  That is definitely a good thing.

Now we wait for what the appellate court has to say.

The Economist debate on the most significant technological development of the 20th century

The Economist has just posted my invited comments on their current debate: "This house believes the development of computing was the most significant technological advance of the 20th century."

As with the last time I was invited to be a "guest speaker" (just one of the oddities of horning an Oxford-style debate into an online shoe), I have difficulty coloring between the lines.  Here are the first couple of graphs of today's contribution:

The development of computing--broadly construed--was indeed the most significant technological advance of the 20th century. New technologies, however, never crop up by themselves, but are instead part of the woven web of human endeavour. There is always more to a given technology than meets the eye.

We often oversimplify "computing" and think only of software or algorithms used to manipulate information. That information comes in units of bits, and our ability to store and crunch those bits has certainly changed our economies and societies over the past century. But those bits reside on a disk, or in a memory circuit, and the crunching of bits is done by silicon chips. Those disks, circuits and chips had to improve so that computing could advance.

Progress in building computers during the mid-20th century required first an understanding of materials and how they interact; from this knowledge, which initially lived on paper and in the minds of scientists and engineers, were built the first computer chips. As those chips increased in complexity, so did the computational power they conferred on computer designers. That computational power was used to design more powerful chips, creating a feedback loop. By the end of the century, new chips and software packages could only be designed using computers, and their complex behaviour could only be understood with the aid of computers.

The development of computing, therefore, required not just development of software but also of the ability to build the physical infrastructure that runs software and stores information. In other words, our improving ability to control atoms in the service of building computers was crucial to advancing the technology we call "computing". Advances in controlling atoms have naturally been extended to other areas of human enterprise. Computer-aided design and manufacturing have radically changed our ability to transform ideas into objects. Our manufactured world--which includes cars, aircraft, medicines, food, music, phones and even shoes--now arrives at our doorsteps as a consequence of this increase in computational power.

I go on to observe that computation is already having an effect on food through increased corn yields courtesy of gene sequencing and expression analysis.

Like so:

Biodesic_US_corn_yield.pngClick through to read the rest.

Hey look -- I have an Idea!

On my head, that is.  Not in, alas, but on.  That's the way it goes, some days.  But at least I am pressing forward.  Or the idea on my head is.  That is what the sign says, anyway. 

carlson.jpgWeek before last, I spent an enjoyable couple of days at The Economist's Ideas Economy: Human Potential 2010.  I'll post the video when it is available.

Among the most interesting things I heard: Richard Florida says that the "creative sector" has never been above 5% unemployment, and that sector now constitutes 30% of the US workforce.  Here is his presentation:

I also had the chance to meet Vivek Wadhwa (very smart fellow), whose recent fascinating blog post on whether job creation comes from big companies or startups I have been pondering for weeks.  Here is a snippet from the post: "Startups aren't just an important contributor to job growth: they're the only thing. Without startups, there would be no net job growth in the U.S. economy. From 1977 to 2005, existing companies were net job destroyers, losing 1 million net jobs per year. In contrast, new businesses in their first year added an average of 3 million jobs annually."

The differing impacts of startups and established companies on the economy and on innovation are much on my mind these last few months.  Unconventional innovation tends to come from startups, and often from garages, and as I examine in my book that is precisely where we should be looking for new biological technologies.  I've been pondering what it takes for a small company developing a biological technology to succeed in industries dominated by Goliaths.  Microbrewing provides a great existence proof of the potential.  Garage biology is here.  Hang on to your hats.

A Few Thoughts on Jury Duty

I spent last week sitting on a jury for King County.  The experience left me with a couple of thoughts about our system of justice.  Also a few thoughts about real estate, the subject of the trial:

1.  Never accept a deal with a dual agent -- one in which the same agent represents both the buyer and the seller.  Shenanigans ensue.

2.  Read all contracts thoroughly.  No more skimming and nodding as if you understand.

3.  Never get into a real estate deal for your primary residence that gets anywhere near taxing your resources.

So much for the plaintiff and the defendant.

And now for the jury system itself.  I had never sat on a jury before, and I am glad I had the experience.  I could have gotten myself excused as a sole proprietor given the expected length of the trial, as did several of my original panel, but I decided I should do my civic duty and give society a week of my time.

So far so good.

But now we have 12 jurors (plus the alternate, during the trial) sitting for a week getting paid all of $10 per day.  And for a trial that basically boiled down to avoidable negligence on the part of the defendant, negligence that wound up costing the plaintiff dearly.  Yes, the defendant deserved to be found negligent, and the plaintiff deserved to be compensated.  And we awarded the plaintiff about $400K in damages, which was no small potatoes in this case.

But having the jury of 12 sit there for a week cost, very roughly, at least $50K in lost salaries and benefits.  To which we must add court costs including salaries, rent, etc., on the courthouse for as long as the case was open (about a year).  I'll bet the citizens of King County (including the jurors) spent nearly as much as the total damages.

In the end, while I certainly acknowledge the importance of jury trials to our democracy, it isn't clear to me that it is a good use of society's resources to spend so much on a case like this.  Perhaps binding arbitration would have served the same ends?  Or maybe that just winds up looking like a trial before a judge?  And the defendant went for trial by jury.

Perhaps this is just the cost we pay for a civil, democratic society.

"Democracy is the worst form of government except for all the others", and all that.

Presidential Bioethics Commission Presentation

Here are the archived video and slides from last week's meeting of the Presidential Commission for the Study of Bioethical Issues.  And here is the session with presentations from Drew Endy, Bonnie Bassler, and myself, followed by questions and discussion with the Commission and public.

Browser warning: When I ran it, something about the combination of Flash and the slide viewer caused Safari to freeze; Firefox was just fine.

Presidential Commission for the Study of Bioethical Issues (Updated, and errata)

Here are the annotated slides (PDF) from my presentation this morning to the Presidential Commission for the Study of Bioethical Issues.  (Update -- A word to the wise; a "crore" is an Indian unit indicating 10,000,000.  We had an errant extra zero in our database, and I have now fixed the Indian biotech GDP number to reflect the correction.)

Now sitting in the audience, I've just heard Jim Thomas of ETC once again egregiously distort the Keasling-Amyris-malaria-artemisinin story.  As usual he is quite well-spoken and reasonable sounding, and uses rhetoric well to his ends.

It may be true, as Thomas asserts, that switching artemisinin production to fermentation will harm the economic livelihood of "a few thousand" (his words) farmers in China and Africa.  But he has left out of his calculation the 40% of the world's population that is at risk of malaria every year.  He has left out the millions of children who die annually from malaria.

Quoting from my book (pg.98 -- I've left out the references as I am liveblogging from the meeting):

The cost burden of the disease on individual families is highly regressive.  The average cost per household for treating malaria may be in the range of only 3-7 percent of income, but total and indirect costs to poor households can amount to one-third of annual income.  The disease also disproportionately affects the young. Approximately 90percent of those who are killed by the parasite are African children under the age of five; according to the World Health Organization (WHO), a child dies from malaria roughly every thirty seconds.

In addition to staggering personal costs, the disease harms whole societies by severely inhibiting economic development. In affected countries, malaria reduces GDP growth by about 1.3 percent per year. These countries, moreover, contain about 40percent of the world's population. Over the past forty years, the growth penalty has created a difference in GDP that substantially exceeds the billions in annual foreign aid they receive. In 2000 the World Health Organization estimated that eliminating this growth penalty in 1965 would have resulted in "up to $100 billion added to sub-Saharan Africa's [2000] GDP of $300 billion. This extra $100 billion would be, by comparison, nearly five times greater than all development aid provided to Africa [in 1999]."

Because there was no technical means to eliminate the parasite in the middle of the twentieth century, this is clearly a number calculated to impress or shock, but the point is that the growth penalty continues to balloon. As of 2008, the GDPs of countries in sub-Saharan Africa would be approximately 35 percent higher than they are today had malaria been eliminated in 1965. The World Health Organization reckons that malaria-free countries have a per capita GDP on average three times larger than malarious countries.  The productivity of farmers in malarious countries is cut by as much as 50 percent because of workdays lost to the disease.  The impact of producing an effective and inexpensive antimalarial drug would therefore be profound.
 
Improving access to other technologies, such as bed nets treated with insecticides, would also be of substantial aid in reducing the rate of infection.  Yet infected victims will still need access to cures. Prevention might be found in a vaccine, which the Gates Foundation also funds. However, even the most promising malaria vaccine candidates are only partially effective and cost even more than artemisinin. Microbial production of artemisinin would completely change the impact of malaria on billions of people worldwide.  Artemisinin is presently derived from the wormwood tree and has been used as an herbal remedy for at least two thousand years. Its antimalarial activity was first described by Chinese scientists in 1971.  The existence of the drug and its physiochemical properties were announced to the world in 1979, although its precise molecular mechanism of action is still not understood. A method for chemical synthesis was published in 1983, but it remains "long, arduous, and economically nonviable."
 
Because natural artemisinin is an agricultural product, it competes for arable land with food crops, is subject to seasonal variations in supply, and its production costs are in part determined by the costs of fertilizer and fuel. As a result of the work of Keasling and his collaborators, it appears that, within just a few years, biological technology may provide a more-flexible and less-expensive supply of drugs than now exists. Commercial production of artemisinin should commence in 2010, with a continuous annual production sufficient to treat the 500million malaria cases per year.

So, Mr. Thomas, what about all the people who will benefit from inexpensive malaria drugs?  It is, frankly, unconscionable and indefensible for you to continue beating this drum as you do.  The human cost of not producing inexpensive artemisinin in vats is astronomical.  If reducing the burden of malaria around the world on almost 2 billion people might harm "a few thousand" farmers, then we should make sure those farmers can make a living growing some other crop.  We can solve both problems.  Your ideological opposition to synthetic biology is is blinding you to the opportunities, and your version of reality would ignore the health and welfare of children around the world.

How's that for rhetoric?

Update:  One other thought.  Just one year of 1.3% GDP growth recovered by reducing (eliminating?) the impact of malaria would more than offset paying wormwood farmers to grow something else.  There is really no argument to do anything else.

For a "Civil Society" organization, ETC is being decidedly uncivil on this issue.