A Brief History of Genetics: How Genetics Transformed Medicine and Identity
Genetics is the study of how genes are transmitted across generations, which includes the genetic information that produces an individual's traits, physical characteristics, and diseases. This recent branch of biology has transformed medicine, agriculture, biotechnology, and pharmacology.
DNA (deoxyribonucleic acid), which contains the blueprint necessary for the development of all living things, is central to heredity and is often the focus of genetics. Genetic testing and genetic engineering are two of the most prominent subfields of the discipline. Genetic testing allows doctors to identify conditions that may require treatment, while genetic engineering allows for the alteration or creation of specific DNA characteristics.
Background
Beginning in the 4th century BCE, the ancient Greeks wondered about the transmission of hereditary traits between generations, suggesting that specific body parts of children were inherited from their parents' corresponding body parts. However, sometimes children looked less like their parents and more like another relative, according to Aristotle (384-322 BCE). He further believed that it was the father who passed along the physical characteristics, while the mother created the appropriate environment, which aided the child's development. Aristotle's ideas, none of which were accurate, included the belief that genetics is passed along via blood. It would be centuries later, especially with the invention of the microscope, which allowed scientists to examine genetic characteristics more closely.
In 1824, French scientist RenΓ© Joachim Henri Dutrochet (1776-1847) concluded that plant and animal tissues were composed of cells, thereby verifying a hypothesis held by scientists since the late 1600s. Additional research in 1838-39 by the German botanist Matthias Jakob Schleiden (1804-1881) and the German cytologist Theodor Schwann (1810-1882) confirmed that cells were the basic unit of life. Both discoveries comprise the cell theory. Later scientists expanded the theory by identifying the various parts of cells, including the nucleus and mitochondria (the nucleus contains the cell's genetic material and regulates the cell's functions, while the mitochondria produce the cell's energy). Additionally, the emerging field of cytology studied the formation, structure, and function of cells and their relationship to cell inheritance. Charles Darwin (1809-1882), the English naturalist, proposed that inherited characteristics are passed from one generation to the next, leading scientists to believe that genetic information is contained in what would later be called germ cells (sperm and eggs).
In the 1760s, Carl Linnaeus (1707-1778), a Swedish taxonomist, was credited with a theory known as hybridization, which showed that a different form of life could be created by combining various kinds of the same species, plants, and animals. Subsequent generations would also inherit these new forms' characteristics. In the late 1700s, French physicians proposed the concept of heredity to explain the physical similarities between parents and their children. By the early 19th century, scientists revealed that physical traits from one parent dominated traits from the other parent and that reproduction between species could be controlled, leading researchers to develop a unitary theory of genetics.
Read More
β A Brief History of Genetics: How Genetics Transformed Medicine and Identity
