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1957

Francis Crick and George Gamov worked out the "central dogma," explaining how DNA functions to make protein. Their "sequence hypothesis" posited that the DNA sequence specifies the amino acid sequence in a protein. They also suggested that genetic information flows only in one direction, from DNA to messenger RNA to protein, the central concept of the central dogma.

Matthew Meselson and Frank Stahl demonstrated the replication mechanism of DNA.

1958 Coenberg discovered and isolated DNA polymerase, which became the first enzyme used to make DNA in a test tube.
1959 Francois Jacob and Jacques Monod established the existence of genetic regulation - mappable control functions located on the chromosome in the DNA sequence - which they named the repressor and operon. They also demonstrated the existence of proteins that have dual specificities.
1961 Marshall Nirenberg built a strand of mRNA comprised only of the base uracil. This strand is called "poly-u," and by examining it Nirenberg discovered that UUU is the codon for phenylalanine. This was the first step in cracking the genetic code, which Nirenberg and colleagues succeeded in doing within five years.
1966 The genetic code was "cracked". Marshall Nirenberg, Heinrich Mathaei, and Severo Ochoa demonstrated that a sequence of three nucleotide bases (a codon) determines each of 20 amino acids.
1967 Mary Weiss and Howard Green took a crucial step in human gene mapping with the publication of a technique for using human cells and mouse cells grown together in one culture. This was called somatic-cell hybridization.
1969 Leonard Herzenberg, a geneticist at Stanford, developed the fluorescence-activated cell sorter, which can identify up to 5,000 closely related animal cells.
1970

Howard Temin and David Baltimore, working independently, first isolated "reverse transcriptase" a restriction enzyme that cuts DNA molecules at specific sites. Their work described how viral RNA that infects a host bacteria uses this enzyme to integrate its message into the host's DNA. This discovery allowed scientists to create clones and observe their function.

1972

Immunologist Hugh McDevitt, in an article in Science, reported observing genes that control immune responses to foreign substances. His observations suggested predictable, inherited susceptibility to some diseases.

The first successful DNA cloning experiments were performed in California.

1973

Scientists for the first time successfully transferred deoxyribonucleic acid (DNA) from one life form into another.

Stanley Cohen and Annie Chang of Stanford University and Herbert Boyer of UCSF "spliced" sections of viral DNA and bacterial DNA with the same restriction enzyme, creating a plasmid with dual antibiotic resistance. They then spliced this recombinant DNA molecule into the DNA of a bacteria, thereby producing the first recombinant DNA organism. Bruce Ames, a biochemist at UC Berkeley, developed a test to identify chemicals that damage DNA. The Ames Test becomes a widely used method to identify carcinogenic substances.


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