Step 1: The DNA of interest and a vector (plasmid) are cut using the same restriction enzyme to create compatible "sticky ends." Step 2: The gene of interest is joined to the vector using the enzyme DNA Ligase, forming Recombinant DNA (rDNA). Step 3: The rDNA is introduced into a host cell (like E. coli) through transformation. The host cells are then cultured at a large scale to produce the desired protein.