Understanding DNA: A Breakthrough in Medicine by Tony Allan

695 Words2 Pages

No one knew how heredity (passing traits) worked until Gregor Mendel, an Austrian monk, crossbred pea plants in his monastery kitchen garden in 1865. In 1869, gene-hunters found rod-like shape in the nucleus of cells that turned red when dye was added. They named this “Chromosome”, from a Greek word, chroma for color. They also went deeper into the cell and discovered a wispy microscopic thread within the chromosomes, which they named DNA. There were several scientists who did not know about Mendel’s breakthrough at the time, but then in 1900, they rediscovered his experiment and old journal copies.

Francis Crick (American) and James D. Watson (Englishman) had a problem with DNA (Deoxyribonucleic Acid) in 1950 because the individual pieces could not be seen. They could be seen with x-ray crystallography which could be done in Kings College, London. They were convinced that DNA was a double helix spiral ladder that contained chemical strands of two to four. It consisted of two strands that were interwoven.

DNA was cracked! They solved the DNA three-dimensional structure at Cambridge, England and were ready to show the first model to their colleagues by March 7th, 1953. They learned how genes worked and how inherited features are passed down from one generation to the next. Their discovery was included in Matt Ridley’s book called Genome. People knew that heredity also affected animals and plants as it does humans. Having red hair or blue eyes gets passed on from one generation to the next one.

Watson met the King’s College team head named Maurice Wilkins, who worked closely with Rosalind Franklin. Rosalind Franklin, a British biophysicist, was the person who discovered the DNA structure using x-ray crystallogr...

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