Timeline: From Darwin and Mendel to the Human Genome Project

  • 1902: Orderly Inheritance of Disease Observed

    1902: Orderly Inheritance of Disease Observed
    Archibald Garrod observes that the disease alkaptonuria is inherited according to Mendelian rules.
  • 1869: DNA First Isolated

    1869: DNA First Isolated
    Friedrich Miescher isolates DNA for the first time.
    Miescher isolated a material rich in phosphorus from the cells and called it nuclein. He found nuclein in other types of cells as well, including salmon sperm.
  • 1909: The Word Gene Coined

    1909: The Word Gene Coined
    Danish botanist Wilhelm Johannsen coined the word gene to describe the Mendelian units of heredity.
  • 1941: One Gene, One Enzyme

    1941: One Gene, One Enzyme
    George Beadle and Edward Tatum, through experiments on the red bread mold Neurospora crassa, showed that genes act by regulating distinct chemical events - affirming the "one gene, one enzyme" hypothesis.
  • 1944: DNA is "Transforming Principle"

    1944: DNA is "Transforming Principle"
    Oswald Avery, Colin MacLeod, and Maclyn McCarty showed that DNA (not proteins) can transform the properties of cells, clarifying the chemical nature of genes
  • 1955: 46 Human Chromosomes

    1955: 46 Human Chromosomes
    Joe Hin Tjio defined 46 as the exact number of human chromosomes.He prepared metaphase spreads that showed the chromosome arrays particularly neatly. He found that all unbroken cells had 46 chromosomes.
  • 1956: Cause of Disease Traced to Alteration

    1956: Cause of Disease Traced to Alteration
    In 1956, Ingram discovered that a specific chemical alteration in a hemoglobin protein - the substitution of valine for glutamic acid in the sixth amino acid in beta globin - is the root of the disease.
  • 1961: First Screen for Metabolic Defect in Newborns

    1961: First Screen for Metabolic Defect in Newborns
    In 1961, Robert Guthrie, a doctor and bacterial scientist at the University of Buffalo Children's Hospital, developed a way to test whether newborn babies have phenylketonuria (PKU), an inability to digest the amino acid phenylalanine.
  • 1966: Genetic Code Cracked

    1966: Genetic Code Cracked
    Marshall Nirenberg, Har Khorana and Severo Ochoa and their colleagues elucidated the genetic code - showing how nucleic acids with their 4-letter alphabet determine the order of the 20 kinds of amino acids in proteins.
  • 1975-77: DNA Sequencing

    1975-77: DNA Sequencing
    Sanger and his colleagues developed a slightly different protocol for sequencing DNA compared with Maxam and Gilbert. Sanger's method, where a marker attaches to the growing ends of DNA chains.
  • 1987: First Human Genetic Map

    1987: First Human Genetic Map
    The first comprehensive genetic map of human chromosomes was based on 400 restriction fragment length polymorphisms (RFLPs).
  • 1990: Launch of the Human Genome Project

    1990: Launch of the Human Genome Project
    The DOE was interested in studying the human genome as a way of aiding the detection of mutations that nuclear radiation might cause. In 1990, DOE and NIH published a plan for the first five years of what was projected to be a 15-year project.
    Goals: mapping the human genome and determining the sequence of all 3.2 billion letters in it; developing technology for analyzing DNA; and studying the ethical, legal and social implications of genome research.