Genetics

>> Tuesday, November 2, 2010

At the beginning of the 20th century, the life sciences entered a period of rapid progress. Mendel’s work in genetics was rediscovered in 1900, and by 1910 biologists had become convinced that genes are located in chromosomes, the threadlike structures that contain proteins and deoxyribonucleic acid (DNA). During the 1940s American biochemists discovered that DNA taken from one kind of bacterium could influence the characteristics of another. From these experiments, it became clear that DNA is the chemical that makes up genes and thus the key to heredity.
After American biochemist James Watson and British biophysicist Francis Crick established the structure of DNA in 1953, geneticists became able to understand heredity in chemical terms. Since then, progress in this field has been astounding. Scientists have identified the complete genome, or genetic catalog, of the human body (see Human Genome Project). In many cases, scientists now know how individual genes become activated and what effects they have in the human body. Genes can now be transferred from one species to another, side-stepping the normal processes of heredity and creating hybrid organisms that are unknown in the natural world.

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