Human artificial chromosomes (HACs) could be useful for gene therapy by allowing large gene fragments to be stably introduced and expressed in target cells without disrupting existing genes. HACs are small, artificial microchromosomes that can carry exogenous DNA and act as entirely new chromosomes in human cells. They were first constructed in 1997 by adding alpha-satellite DNA to telomeric and genomic DNA. There are two accepted methods for creating HAC vectors - altering a natural chromosome or de novo construction of a novel chromosome, though the latter has proven more difficult. HACs are preferable to other transgenic methods like yeast/bacterial artificial chromosomes due to their separation from the original genome, which provides greater stability and prevents insert