Brief History of Maize Domestication StudiesResearch on maize domestication has attracted a great deal of interest over the last century, including the attention of two Nobel laureates. Of primary interest is the evolutionary question of how maize was domesticated from a wild relative that differs so dramatically in ear and plant morphology. The study of maize domestication can be divided into two main periods: 1. Competing Hypotheses: The first period began in the 1930s when George Beadle and Paul Mangelsdorf proposed two contrasting hypotheses for the origin of maize. Beadle proposed the "Teosinte Hypothesis" in which maize is simply a domesticated form of teosinte. He believed that, through artificial selection by ancient populations, several small mutations with relatively large effects could have transformed teosinte into maize. In contrast, Mangelsdorf suggested maize was the product of a hybridization between an undiscovered wild maize and Tripsacum, known as the "Tripartite Hypothesis." From its debut in 1938 until the 1960s, the Tripartite Hypothesis was widely accepted. Through productive collaborations with prominent archaelogists of his day and widespread efforts targeting maize germplasm conservation, Mangelsdorf was able to publicize his theory among a wide audience. Upon his "retirement" in 1968, however, George Beadle rejoined the maize controversy and vigorously championed the Teosinte Hypothesis. His own genetic research, followed by chromosomal studies by McClintock and Kato and morphological systematics by Iltis, would eventually convince the majority of biologists of the Teosinte Hypothesis. Although revisions of the Tripartite Hypothesis were suggested by Mangelsdorf in the 1980s and again by Eubanks in the 1990s, no convincing molecular genetic evidence has ever been found to support these revised Tripsacum hypotheses. 2. The Genome: The second period began in the late 1960s when researchers focused their attention on describing the diversity and evolutionary relationships within the genus Zea, and on determining those genes involved in domestication and the evolution of the genome. Garrison Wilkes published the first thorough monograph on teosinte in 1967. Hugh Iltis, John Doebley, Rapheal Guzman, and B. Pazy invigorated teosinte research by discovering and describing the perennial species Z. diploperennis. In 1980, Iltis and Doebley established an organized taxonomy that considered the probable evolutionary relationships between taxa. McClintock and Kato synthesized and published chromosomal knob diversity data that had been collected over the previous 30 years in 1981. Throughout the 1980s and 1990s, Charles Stuber and Major Goodman's research groups produced comprehensive analyses of isozyme diversity in over 1000 maize races and in almost all known teosinte populations. With the advent of DNA analysis and sequencing in the 1980s, John Doebley, Ed Buckler, and Brandon Gaut refined the phylogenetic relationships among grasses and the genus Zea, contributing to our understanding of how the genome has evolved. Beginning in the 1990s, John Doebley's research group began to discover some of the genes involved in maize domestication. Biologists: Beadle | Mangelsdorf | McClintock | Iltis | Galinat | Wilkes | Kato | Goodman | Stuber | Doebley | Gaut | Buckler | Eubanks | Sanchez | Bretting Archaeologists: MacNeish | Lathrap | Flannery | Pearsall | Piperno | Benz | Bird | Lamkey | Labate
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