Cosmid vectors have been developed which carry selective markers for growth in bacteria (beta lactamase gene) and animal cells (the Herpes Simplex virus thymidine kinase gene, the transposon Tn-5 aminoglycosyl 3' phosphotransferase gene and the E. coli guanine phosphoribosyltransferase gene). The design of the cosmids allows the exchange of the eukaryotic markers in recombinant cosmids. Human and mouse cosmid libraries containing DNA inserts of about 40kb have been generated by an improved method. Several clones from the human beta-globin locus were isolated. These cosmids transform mouse L cells at high efficiency in both circular and linear form. The newly introduced genes are expressed accurately in L cells.

0 (DNA, Recombinant), 0 (Plasmids), 0 (RNA, Messenger), 9004-22-2 (Globins), Animals, Bacteria/genetics, Chromosomes, Cloning, Molecular, DNA Restriction Enzymes, DNA, Recombinant, EC 3.1.21 (DNA Restriction Enzymes), Globins/genetics, Human, L Cells (Cell Line)/physiology, Mice, Plasmids, RNA, Messenger/genetics, Support, Non-U.S. Gov't, Transformation, Genetic
hdl.handle.net/1765/2362
Nucleic Acids Research
Erasmus MC: University Medical Center Rotterdam

Grosveld, F.G, Lund, T, Murray, E.J, Mellor, A.L, Dahl, H.H.M, & Flavell, R.A. (1982). The construction of cosmid libraries which can be used to transform eukaryotic cells. Nucleic Acids Research, 10(2), 6715–6732. Retrieved from http://hdl.handle.net/1765/2362