The Nobel Prize: Winners who’ve advanced the study of genetics
An annual tradition since 1901, Nobel Prize winners will be announced throughout this week in recognition of individuals who—in the words of Alfred Nobel—have ”conferred the greatest benefit to mankind.” In the past, Prizes in Chemistry and Medicine have been awarded to researchers studying topics that range from organic chemical reactions to the ways in which DNA codes for life. In fact, 215 have been awarded in these categories between the years of 1901 and 2016.
Once again, research with a genetic impact is taking center stage at the Nobel ceremony this year. The 2017 Nobel Prize in Physiology or Medicine was awarded today to Jeffrey C. Hall, Michael Rosbash, and Michael W. Young for foundational research describing our inner circadian clock, the mechanism in our body that drives wakefulness and sleepiness. This research set the stage for numerous scientific advancements in the field of circadian rhythms and underpins products like Exploragen’s SlumberType and MySleepInsights by MyVytalics. (For more information on how genetics and your circadian rhythm interact, check out our recent blog post on the topic.)
In honor of this exciting week, we wanted to recap some of the past prizes for work that has contributed to the science behind Helix.
Albrecht Kossel, 1910
Awarded the Nobel Prize for his chemical descriptions of deoxyribonucleic acids (DNA) and ribonucleic acids (RNA). Thanks to his research, the world learned about the nitrogen bases that comprise DNA and RNA—Adenine, Thymine, Guanine, Cytosine, and Uracil, often represented by A, T, G, C, and U, respectively. At Helix, our logo represents the 4 nitrogenous bases of DNA (A, T, G, and C), so we owe an especially big “thank you” to Dr. Kossel.
Thomas H. Morgan, 1933
Awarded the Nobel Prize for his work studying the way that heritable information is organized and passed on to the next generation. His famous Fly Room at Columbia University produced numerous foundational discoveries in the nascent field of genetics, and some terminology around mapping genetic information is named after him.
George Wells Beadle, Edward Lawrie Tatum, and Joshua Lederberg, 1958
Awarded the Nobel Prize for their research findings showing that DNA sequences contain information required to make proteins. Your DNA is a series of nucleotides which, when aligned in a specific pattern, spell out a code. This code contains information that instructs cells on how to build proteins and how to function. In short, DNA contains instructions for building life.
Severo Ochoa and Arthur Kornberg, 1959
Ochoa and Kornberg’s work described how new copies of DNA and RNA are made. Severo Ochoa was the first to make RNA in a test tube using an enzyme from bacteria. Arthur Kornberg, one of Ochoa’s former students, later isolated and identified the enzyme that makes new copies of DNA. Aside from the discoveries themselves, the methods they used to methodically isolate and purify enzyme activity defined a generation of biochemists, with several of their academic “children” (and Kornberg’s actual children) winning later Nobel Prizes of their own.
Francis Crick, James Watson, and Maurice Wilkins, 1962
Crick, Watson, and Wilkins are perhaps some of the most well-known Nobel laureates. Rosalind Franklin and Maurice Wilkins used an advanced technology known as X-ray crystallography to generate abstract images (something you can try at home!) based on the way that X-rays are scattered as they pass through DNA. Using the data from Franklin and Wilkins, Watson and Crick were able to determine the double-stranded structure of DNA. This structure is the basis for how information in DNA is stored, copied, and accessed.
Robert W. Holley, Har Gobind Khorana, and Marshall W. Nirenberg, 1968
Awarded the Nobel Prize for their collective findings describing how information in the DNA sequence is coded. Scientists had previously known the DNA contained information for making proteins, but the code itself was not yet known. Thanks to the work of these scientists, we now understand that DNA sequences are segmented into discrete 3-base units, known as codons. Codons are the equivalent of words in a sentence. Codons are placed together to spell out a sentence which, in this analogy, would equate to a protein. (We highlighted the work and life of Dr. Har Gobind Khorana for Asian American and Pacific Islander Heritage Month. Learn more about this influential scientist here.)
Paul Burg, Walter Gilbert, and Frederick Sanger, 1980
Awarded the Nobel Prize for their role in developing scientific methods that allow us to determine the sequence of DNA. Reading the DNA sequence allows us to understand how many genes we have and what they do. We still use the basic concept of this method today. (An interesting side note: this was Sanger’s second Nobel prize. In 1958, he won for studying the structure of proteins and insulin.)
Barbara McClintock, 1983
Awarded the Nobel Prize for her work describing the ability of DNA to move between locations within the genome. Her studies using maize (a type of corn) introduced the scientific world to a new notion: small segments of DNA can be moved to other regions, and that some genes directly influence the activity of other genes. These mobile DNA elements are left over from a virus millions of years ago, and they’ve helped shape our evolution by making extra copies of some genes and breaking others. The concept of genetic regulation that she discovered might seem mundane today, but it was a decade before other researchers would replicate the discovery in bacteria. Read more about her impact here.
Ready to learn what your DNA has to say about your bedtime? Both MySleepInsights from MyVytalics and Slumbertype from Exploragen are here to help.
Kary B. Mullis and Michael Smith, 1993
Awarded the Nobel prize for their work in establishing scientific methods that allow us to study particular regions of the DNA. Mullis developed a technique known as PCR. This method is used to make numerous copies of a specific region of DNA, which allows us to study DNA from a small sample and is currently used throughout biomedical science. Smith determined how to introduce specific changes in a given DNA sequence. Having this ability helps us to study specific DNA variants in the lab and ultimately determine how changes in the DNA affect a protein’s function.
Roger Kornberg, 2006
Son of Arthur Kornberg who shared the 1959 Prize, Roger won for his work in describing and imaging proteins responsible for reading DNA. At the time of this discovery, the physical mechanisms by which cells read the DNA to make proteins was unclear. Using complex imaging techniques, Roger Kornberg imaged multiple steps in this process and shed invaluable light on a critical process found in all living organisms.
Elizabeth Blackburn, Carol Greider, and Jack Szostak, 2009
Won the Nobel Prize for their work describing the structure and maintanence of telomeres, regions of DNA located at the ends of chromosomes. Telomeres are similar in concept to the plastic caps on the ends of shoelaces: they protect the DNA from wear and tear during the process of making a new cell. This process is inherently flawed, because every time a cell replicates, small portions of DNA are deleted from the chromosome ends. This would be catastrophic for a cell, but, telomeres serve as a buffer zone—a disposable DNA sequence that can be incrementally deleted while having little effect on cell health. Telomeres, and the proteins that replenish them, have since been shown to play critical roles in human health.
To see all the winners, be sure to visit the official Nobel Prize website.