Biopolym. Cell. 1989; 5(6):87-92.
Gene-Engineering Biotechnology
A fast method for cloning of specific cDNA. Cloning of human prolactin cDNA
1Zolotukhin S. B., 1Markelova E. Yu., 1Panasenko G. V., 1Naidenov V. G., 1Shved A. D., 2Sautin Yu. Yu., 3Patsko Ya. V.
  1. Institute of Molecular Biology and Genetics, Academy of Sciences of the Ukrainian SSR
    Kiev, USSR
  2. Institute of Neurosurgery, Ministry of Public Health of the Ukrainian SSR
    Kiev, USSR
  3. Lvov Branch of A. V. Palladin Institute of Biochemistry, Academy of Sciences of the Ukrainian SSR
    Lvov, USSR

Abstract

A method allowing fast and effective cloning of particular cDNA is described. Pairs of synthetic oligonucleotides-primers are used for polymerize chain reaction mediated selective amplification of prolactine cDNTA synthesized on human pituitary poly (A)-mRNA. Sequence of one of the recombinant plasmid insert revealed a full-length pro-lactin cDNA, flanked by the synthetic primers.

References

[1] Schmid A, Cattaneo R, Billeter MA. A procedure for selective full length cDNA cloning of specific RNA species. Nucleic Acids Res. 1987;15(10):3987-96.
[2] Saiki RK, Gelfand DH, Stoffel S, Scharf SJ, Higuchi R, Horn GT, Mullis KB, Erlich HA. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988;239(4839):487-91.
[3] Atkinson T, Smith M. Solid phase synthesis of oligo-deoxyribonucleotides by phosphate- triester method. Oligonucleotide synthesis. A practical approach . Ed. M. J. Gait. New York: IR1L Press, 1984:35-82.
[4] Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987;162(1):156-9.
[5] Aviv H, Leder P. Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose. Proc Natl Acad Sci U S A. 1972;69(6):1408-12.
[6] Maniatis T, Fritsch EF, Sambrook J. Molecular cloning - a laboratory manual. New York, Cold SPring Harbor, 1982; 545 P.
[7] Gubler U, Hoffman BJ. A simple and very efficient method for generating cDNA libraries. Gene. 1983;25(2-3):263-9.
[8] Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977;74(12):5463-7.
[9] Zhang H, Scholl R, Browse J, Somerville C. Double stranded DNA sequencing as a choice for DNA sequencing. Nucleic Acids Res. 1988;16(3):1220.
[10] Evans GA, Hucko J, Rosenfeld MG. Preprolactin represents the initial product of prolactin mRNA translation. Endocrinology. 1977;101(6):1807-14.
[11] Mashko SV, Lapidus AL, Trukhan ME, Lebedeva MI, Podkovyrov SM. Creation of artificial hybrid operons with partially overlapping genes to achieve an expression of heterologous genes in Escherichia coli cells. Mol Biol (Mosk). 1987;21(5):1297-309.
[12] Cooke NE, Coit D, Shine J, Baxter JD, Martial JA. Human prolactin. cDNA structural analysis and evolutionary comparisons. J Biol Chem. 1981;256(8):4007-16.
[13] Mertvetsov NP, Golovin SIa, Zelenin SM, Morozova TV, Karginov VA. Synthesis, cloning and determination of the primary structure of DNA complementary to mRNA of prolactin from the human pituitary gland. Bioorg Khim. 1987;13(12):1687-90.
[14] Lu X, Werner D. Construction and quality of cDNA libraries prepared from cytoplasmic RNA not enriched in poly(A)+RNA. Gene. 1988;71(1):157-64.
[15] Beliavskii AV, Raevskii K. Amplification of total cDNA in vitro. Dokl Akad Nauk SSSR. 1988;303(6):1498-501. Russian.
[16] Frohman MA, Dush MK, Martin GR. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc Natl Acad Sci U S A. 1988;85(23):8998-9002.