1. DNA is isolated from cell by centrifugation then the gene of interest is amplified by PCR, then theres a vector that will carry the gene usually a plasmid
2. digestion with restriction enzyme - the DNA and vector are cut using a restriction enzyme, it cuts the sugar phosphate backbone to create blunt ends or sticky ends
3. gene of interest is inserted into the plasmid then the gene and vector are spliced and DNA ligase joins the gene and vector by fusing the sugar-phosphate backbones together by a covalent phosphodiester bond