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What Is Genetics?

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Genetics can be simply defined as the manipulation of DNA to study cellular and organismal functions. Since DNA encodes all of the information needed to make the cell and the complete organism, the effects of changes in DNA can give clues to the normal functions of the cell and organism.

Before the advent of methods for manipulating DNA in the test tube, the only genetic approaches available for studying cellular and organismal functions were those of classical genetics. In this type of analysis, mutants (i.e., individuals that differ from the normal, or wild-type, members of the species by a certain observable attribute, or phenotype) that have alterations in the function being studied are isolated. The changes in the DNA, or mutations, responsible for the altered function are then localized in the chromosome by genetic crosses. The mutations are then grouped into genes to determine how many different genes are involved. The functions of the genes can then sometimes be deduced from the specific effects of the mutations on the organism. The ways in which mutations in genes involved in a biological system can alter the biological system provide clues to the normal functioning of the system.

Classical genetic analyses continue to contribute greatly to our understanding of developmental and cellular biology. A major advantage of the classical genetic approach is that mutants with an altered function can be isolated and characterized without any a priori understanding of the molecular basis of the function. Classical genetic analysis also is often the only way to determine how many gene products are involved in a function and, through suppressor analysis, to find other genes whose products may interact either physically or functionally with the products of these genes.

The development of molecular genetic techniques has greatly expanded the range of methods available for studying genes and their functions. These techniques include methods for isolating DNA and identifying the regions of DNA that encode particular functions, as well as methods for altering or mutating DNA in the test tube and then returning the mutated DNA to cells to determine the effect of the mutation on the organism.

The approach of first cloning a gene and then altering it in the test tube before reintroducing it into the cells to determine the effects of the alterations is sometimes called reverse genetics and is essentially the reverse of a classical genetic analysis. In classical genetics, a gene is known to exist only because a mutation in it has caused an observable change in the organism. With the molecular genetic approach, a gene can be isolated and mutated in the test tube without any knowledge of its function. Only after the mutated gene has been returned to the organism does its function become apparent.

Rather than one approach supplanting the other, molecular genetics and classical genetics can be used to answer different types of questions, and the two approaches often complement each other. In fact, the most remarkable insights into biological functions have often come from a combination of classical and molecular genetic approaches.

Snyder and Champness Molecular Genetics of Bacteria

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