Welcome to the Genome. Michael Yudell

Welcome to the Genome - Michael Yudell


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to articulate a prescient and stirring vision of what was to come in molecular biology.

      Schrodinger’s call to biologists posed the central question of What is Life?:

      How can the events in space and time which take place within the spatial boundary of a living organism be accounted for by physics and chemistry? (3)

      Schrodinger’s reduction of life to the laws of physics and chemistry need not be read as a deterministic view of the primacy of genetic heredity over the other factors that determine an individual (i.e., the components of a person’s environment). After all, the question of his book is “What is life?” and not “What makes us human?” or “What is the meaning of life?” Instead, Schrodinger was after something much more basic—the substances and rules that determine genetic heredity—that from a physicist’s viewpoint was essential to understanding life. The discoveries discussed in this chapter reflect Schrodinger’s conviction that the substance of life can be reduced to interplay between physics and chemistry. Yet, although these discoveries illustrate the mechanistic nature of genetic heredity, they cannot paint a complete picture of why we are the way we are. “The answer to What is Life?” the evolutionary biologist Stephen Jay Gould reminds us, “requires attention to more things on earth than are dreamed of in Schrodinger’s philosophy.” (6)

      This chapter examines some of the essential components of the gene sequencing puzzle (through the twentieth century) and of the growing general understanding of the mechanisms of heredity. Today we can look back on these discoveries and see how they are like stations along an assembly line, making up separate pieces that are all essential to the overall product of gene sequencing. In Chapter 3 we will see how all of these technologies came together to give us the technology that sequenced the human genome.

      Nearly 50 years passed between the discovery of the double helix and the sequencing of the human genome. Some of the earliest techniques developed by scientists working on the problems of genetic heredity so closely resemble methods used by contemporary genome scientists that it may seem surprising that it took so long to complete the human gene sequence. But molecular biology was still in its infancy in the 1950s, and the technological advances necessary to sequence a whole genome would still take decades to come to fruition.

      The method developed by Sanger exploited the chemistry of amino acids and proteins that had been well known for over 10 years. Just as nucleotides are the building blocks of DNA, amino acids are the building blocks of proteins. Sanger himself wrote in the journal Science:

      In 1943 the basic principles of protein chemistry were firmly established. It was known that all proteins were built up from amino acid residues bound together by peptide bonds to form long polypeptide chains. Twenty different amino acids are found in most mammalian proteins, and by analytical procedures it was possible to say with reasonable accuracy how many residues of each one was present in a given protein. (9)

Diagram displaying a primary structure consists of amino acids 1, 2, and 4 linked by lines to a secondary structure with an arrow linking to a tertiary structure leading to a quaternary structure of a hemoglobin molecule.

       Credit: Wiley Publishers

Photo of Frederick Sanger.

      Credit: https://commons.wikimedia.org/wiki/File:Frederick_Sanger2.jpg

      Sanger’s challenge was to figure out a way to read the order of the amino acids that determine a protein. For his experiments Sanger chose to use bovine, or cow, insulin because of its important medical significance and its relatively short length—only 105 amino acids. Sanger set out to find ways to read the unwieldy molecule, which by his method could be deciphered only by breaking the protein apart, looking at small stretches of four or five amino acids, and then conceptually putting the molecule back together like a puzzle to determine the full sequence.

      Sanger determined that the exposure of insulin to certain chemicals could break the peptide bonds in a protein chain. Sanger was able to identify the kinds of amino acids these broken‐down parts contained. He then created groups of small chains of amino acids that could be “tiled,” or pieced together, to give a full‐length sequence of a protein. (10)

      Sanger was considered to be “reticent, even shy, a man who worked with his hands, at the laboratory bench.” (11) Yet he also recognized the impact that his work would have on science and medicine.


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