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Douglas C. Wallace: The Mitochondrial Maestro
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17315 |
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Section : |
NATURAL SCIENCE
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| Issue
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2 / 1990 |
3,110 Words |
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James Vickers James Vickers teaches English at East Carolina University in
Greenville, North Carolina. |
By the time Gregor Mendel began the pea-breeding experiments in 1856 that would lead to his discovery of the basic laws of inheritance, scientists already knew that the cell was a complex heterogeneous unit consisting of a nucleus and an indeterminate umber of additional subunits. In 1897, the German biologist Carl Benda identified one of those subunits, which he called the mitochondrion, Greek for "filament granule."
Aided by advanced microscopes and methodology, scientists soon discovered that the term inaccurately describes the small, sausage-shaped structures. In the post-World War II years the electron microscope revealed the complex inner structure of the mitochondrion, enabling biochemists to identify the enzymes that control the chemical reactions providing the energy that allows plants and animals to function.
Thereafter, investigation of the mitochondria was progressing slowly until 1971, when Douglas C. Wallace, a 25-year-old biochemist doing predoctoral research at Yale University, began studies that he continues today as the head of a 12-member team at Emory University in Atlanta. During the last six years, those studies have yielded striking results, offering new insights into inheritance, the origins of humankind, and the causes of a series of degenerative diseases.
Well over 99 percent of the DNA in each cell resides in the nucleus, but each cell contains several hundred mitochondria in the cytoplasm surrounding the nucleus. Each mitochondrion contains several copies of its own DNA (mtDNA). This mtDNA has a unique genetic code and is capable of mutation. However, the mtDNA differs radically from the nuclear DNA (nDNA).
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