While recombinant DNA technology allows joining DNA segments from different species (e.g., inserting a gene from one species into a plasmid or chromosome of another to create a transgenic organism), creating an entire functional chromosome de novo by simply joining arbitrary "segments of DNA taken from cells of different species" is significantly more complex. A functional chromosome requires precise organization of elements like origins of replication, centromeres, and telomeres that are species-specific in their function and interaction with cellular machinery. Simply joining random segments from different species is unlikely to yield a functional chromosome capable of stable replication and segregation within a cell.