DNA TIMELINE

  • Natural Selection

    Natural Selection
    Charles Darwin wrote “On the Origin of Species by Means of Natural Selection, or the Preservation of Favored Races in the Struggle for Life.
  • Heredity Transmitted in Units

    Gregor Mendel’s experiments on peas demonstrate that heredity is transmitted in discrete units.
  • DNA Isolated

    DNA Isolated
    Rederick Miescher isolates DNA from cells for the first time and calls it “nuclein”.
  • Discovery: Mitosis

    Described Walter Flemming describes chromosome behavior during animal cell division. He stains chromosomes to observe them clearly and describes the whole process of mitosis in 1882.
  • Rediscovery of Mendel’s work

    Rediscovery of Mendel’s work
    Botanists DeVries, Correns, and von Tschermak independently
    rediscover Mendel’s work while doing their own work on the
    laws of inheritance. The increased understanding of cells and
    chromosomes at this time allowed the placement of Mendel’s
    abstract ideas into a physical context.
  • Chromosome Theory of Inheritance

    Walter Sutton observes that the segregation of chromosomes
    during meiosis matched the segregation pattern of Mendel’s
  • Orderly Inheritance of Disease 1902

    Orderly Inheritance of Disease 1902
    A British physician, Archibald Garrod, observes that the
    disease alkaptonuria is inherited according to Mendelian rules.
    This disease involves a recessive mutation, and was among the
    first conditions ascribed to a genetic cause.
  • The Word Gene is Coined

    The Word Gene is Coined
    Wilhelm Johannsen coins the word “gene” to describe the
    Mendelian unit of heredity. He also uses the terms genotype
    and phenotype to differentiate between the genetic traits of an
    individual and its outward appearance.
  • Chromosomes Carry Genes

    Chromosomes Carry Genes
    Thomas Hunt Morgan and his students study fruit fly
    chromosomes. They show that chromosomes carry genes, and
    also discover genetic linkage.
  • One Gene, One Enzyme Hypothesis

    George Beadle and Edward Tatum’s experiments on the red
    bread mold, Neurospora crassa, show that genes act by
    regulating distinct chemical events. They propose that each
    gene directs the formation of one enzyme
  • DNA Has a Regular Periodic Structure

    DNA Has a Regular Periodic Structure
    William Astbury, a British scientist, obtains the first X-ray
    diffraction pattern of DNA, which reveals that DNA must
    have a regular periodic structure. He suggests that nucleotide
    bases are stacked on top of each other.
  • DNA Transforms Cells

    Oswald Avery, Colin MacLeod, and Maclyn McCarty show
    that DNA (not proteins) can transform the properties of cells --
    thus clarifying the chemical nature of genes.
  • Jumping Genes

    Jumping Genes
    Barbara McClintock, using corn as the model organism,
    discovers that genes can move around on chromosomes. This
    shows that the genome is more dynamic than previously
    thought. These mobile gene units are called transposons and
    are found in many species.
  • Genes Are Made of DNA

    Alfred Hershey & Martha Chase show that only the DNA of a
    virus needs to enter a bacterium to infect it, providing strong
    support for the idea that genes are made of DNA
  • DNA Double Helix

    DNA Double Helix
    Francis H. Crick and James D. Watson described the double
    helix structure of DNA. They receive the Nobel Prize for their
    work in 1962.
  • 46 Human Chromosomes

    Joe Hin Tjio defines 46 as the exact number of chromosomes in
    human cells.
  • DNA copying enzyme

    DNA copying enzyme
    Arthur Kornberg and colleagues isolated DNA polymerase, an
    enzyme that would later be used for DNA sequencing.
  • Cause of Disease Traced to Alteration

    Cause of Disease Traced to Alteration
    Vernon Ingram discovers that a specific chemical alteration in
    a hemoglobin protein is the cause of sickle cell disease.
  • Semiconservative Replication of DNA

    Matthew Meselson and Franklin Stahl demonstrate that DNA
    replicates semiconservatively: each strand from the parent
    DNA molecule ends up paired with a new strand from the
    daughter generation.
  • Chromosome Abnormalities Identified

    Chromosome Abnormalities Identified
    Jerome Lejeune and his colleagues discover that Down
    Syndrome is caused by trisomy 21. There are three copies,
    rather than two, of chromosome 21, and this extra
    chromosomal material interferes with normal development.
  • First Screen for Metabolic Defect in Newborns

    Robert Guthrie develops a method to test newborns for the
    metabolic defect, phenylketonuria (PKU).
  • mRNA Ferries Information

    mRNA Ferries Information
    Sydney Brenner, François Jacob and Matthew Meselson
    discover that mRNA takes information from DNA in the
    nucleus to the protein-making machinery in the cytoplasm.
  • Genetic Code Cracked

    Marshall Nirenberg and others figure out the genetic code
    that allows nucleic acids with their 4 letter alphabet to
    determine the order of 20 kinds of amino acids in proteins.
  • First Restriction Enzyme Described

    First Restriction Enzyme Described
    Scientists describe restriction nucleases, enzymes that
    recognize and cut specific short sequences of DNA. The
    resulting fragments can be used to analyze DNA, and these
    enzymes later became an important tool for mapping
    genomes.
  • First recombinant DNA

    Scientists produce recombinant DNA molecules by joining
    DNA from different species and subsequently inserting the
    hybrid DNA into a host cell, often a bacterium.
  • First animal gene cloned

    First animal gene cloned
    Researchers fuse a segment of DNA containing a gene from
    the African clawed frog Xenopus with DNA from the
    bacterium E. coli and placed the resulting DNA back into an
    E. coli cell. There, the frog DNA was copied and the gene it
    contained directed the production of a specific frog protein.
  • DNA Sequencing

    Two groups, Frederick Sanger and colleagues, and Alan
    Maxam and Walter Gilbert, both develop rapid DNA
    sequencing methods. The Sanger method is most commonly
    employed in the lab today, with colored dyes used to identify
    each of the four nucleic acids that make up DNA
  • First Genetic Engineering Company

    First Genetic Engineering Company
    Herbert Boyer founds Genentech. The company produces the
    first human proteinin a bacterium, and by 1982 markets the
    first recombinant DNA drug, human insulin.
  • Introns Discovered

    Richard Roberts’ and Phil Sharp’s labs show that eukaryotic
    genes contain many interruptions called introns. These noncoding
    regions do not directly specify the amino acids that
    make protein products.
  • First Transgenic Mice and Fruit Flies

    First Transgenic Mice and Fruit Flies
    Scientists successfully add stably inherited genes to laboratory
    animals. The resulting transgenic animals provide a new way
    to test the functions of genes.
  • GenBank Database Formed

    Scientists begin submitting DNA sequence data to a National
    Institutes of Health (NIH) database that is open to the public.
  • First Disease Gene Mapped

    First Disease Gene Mapped
    A genetic marker for Huntington’s disease is found on
    chromosome 4.
  • PCR Invented

    PCR Invented
    The polymerase chain reaction, or PCR, is used to amplify
    DNA. This method allows researchers to quickly make billions
    of copies of a specific segment of DNA, enabling them to study
    it more easily.
  • First Time a Disease Gene is Positionally Cloned

    First Time a Disease Gene is Positionally Cloned
    A method for finding a gene without the knowledge of the
    protein it encodes is developed. So called, positional cloning
    can help in understanding inherited disease, such as muscular
    dystrophy.
  • First Human Genetic Map

    The first comprehensive genetic map is based on variations in
    DNA sequence that can be observed by digesting DNA with
    restriction enzymes. Such a map can be used to help locate
    genes responsible for diseases.
  • Yeast Artificial Chromosomes

    Yeast Artificial Chromosomes
    Scientists discover that artificial chromosomes made from
    yeast can reliably carry large fragments of human DNA
    containing millions of base-pair pieces. Earlier methods used
    plasmids and viruses, which can carry only a few thousand
    base-pair pieces. The ability to deal with much larger pieces
    of DNA makes mapping the human genome easier.
  • Microsatellites Are New Genetic Markers

    Repetitive DNA sequences called microsatellites are used as
    genetic landmarks to distinguish between people. Another type
    of marker, sequence–tagged sites, are unique stretches of DNA
    that can be used to make physical maps of human
    chromosomes.
  • Launch of the Human Genome Project

    Launch of the Human Genome Project
    The Department of Energy and the National Institutes of
    Health announce a plan for a 15-year project to sequence the
    human genome. This will eventually result in sequencing all 3.2
    billion letters of the human genome.
  • ESTs, Fragments of Genes

    An expressed-sequence tag (EST) an identified piece of a gene,
    is made by copying a portion of a messenger RNA (mRNA)
    molecule. As such, ESTs provide a way to focus on the
    “expressed” portion of the genome, which is less than one-tenth
  • Second-Generation Genetic Map of Human Genome

    Second-Generation Genetic Map of Human Genome
    A French team builds a low-resolution, microsatellite genetic
    map of the entire human genome. Each generation of the map
    helps genetics.
  • FLAVR SAVR Tomato

    The Food And Drug Administration approves the sale of the
    first genetically modified food.
  • Ban on Genetic Discrimination in the Workplace

    Ban on Genetic Discrimination in the Workplace
    Protection under the American with Disabilities Act is
    extended to cover discrimination based on genetic
    information.
  • Mouse Genetic Map Completed

    The lab mouse is valuable for genetics research because
    humans and mice share almost all of their genes, and the
    genes on average are 85% identical. The mouse genetic
    increases the utility of mice as animal models for genetic
    disease in humans.
  • E. coli Genome Sequenced

    E. coli Genome Sequenced
    The complete sequence of the E. coli genome will help
    scientists learn even more about this extensively studied
    bacterium
  • M. tuberculosis Bacterium Sequenced

    Mycobacterium tuberculosis causes the chronic infectious
    disease tuberculosis. The sequencing of this bacterium is
    expected to help scientists develop new therapies to treat the
    disease.
  • Roundworm C. elegans Sequenced

    Roundworm C. elegans Sequenced
    The first genome sequence of a multicellular organism, the
    round worm, Caenorhabditis elegans, is completed.
  • Chromosome 22 Sequenced

    Chromosome 22 Sequenced
    The first finished, full-length sequence of a human chromosome
    is produced. Chromosome 22 was chosen to be first because it is
    relatively small and had a highly detailed map already
    available. Such a map is necessary for the clone by clone
    sequencing approach.
  • Human Genome Working Draft Completed

    Human Genome Working Draft Completed
    By the end of Spring 2000, HGP researchers sequence 90
    percent of the human genome with 4-fold redundancy. This
    working draft sequence is estimated to be 99.9% accurate
  • Mouse Genome Working Draft Assembled and Analyzed

    The Mouse Genome Sequencing Consortium publishes an
    assembled draft and comparative analysis of the mouse
    genome. This milestone was originally planned for 2003.
  • Rat Genome Working Draft Completed

    Rat Genome Working Draft Completed
    By Fall 2002, researchers sequence over 90% of the rat genome
    with over 5-fold redundancy.
  • Completion of the Human Genome Sequencing

    Completion of the Human Genome Sequencing
    The finished human genome sequence will be at least 99.99%
    accurate.
  • Identical twins have differences in their genetic

    Identical twins have differences in their genetic
    DNA Worldwide and Eurofins Forensic discover identical twins have differences in their genetic makeup In 2013, DNA Worldwide and their laboratory partners Eurofins Forensic were the first in the world to prove that twins have differences in their genetic makeup.
  • Creation of an organism with an expanded artificial genetic code

    Further Breakthroughs Throughout 2014 the world’s scientists have continued to develop their understanding of DNA. Researchers announced in May that they had successfully created an organism with an expanded artificial genetic code. This success could eventually lead to the creation of organisms that can produce medicines or industrial products organically.