Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1973 Jun;70(6):1697–1700. doi: 10.1073/pnas.70.6.1697

A General Method of Gene Isolation

Thomas Y Shih 1, Malcolm A Martin 1
PMCID: PMC433575  PMID: 4352649

Abstract

A general method of gene isolation has been developed that involves the chemical linkage of RNA to cellulose by a water-soluble carbodiimide, and the continuous circulation of DNA containing specific sequences complementary to the RNA. The temperature of the cellulose matrix is maintained at 37° (50% formamide, 0.3 M NaCl-0.03 M Na3 citrate) to allow efficient DNA-RNA interaction in the stationary phase, while unreacted and any reassociated DNA is denatured at 90° and then recirculated into the hybridization chamber. Between 40 and 45% of fragmented 32P-labeled simian virus (SV)40 DNA was removed from the circulating solution when cellulosebound SV40-specific RNA, assymmetrically transcribed in vitro with Escherichia coli RNA polymerase, was used. In the presence of 104-fold excess of sheared E. coli DNA, nearly half of the [32P]SV40 DNA was recovered from the mixture as a DNA-RNA hybrid with negligible contamination by bacterial DNA. The isolation procedure is almost quantitative for the complementary DNA. The efficiency and selectivity of this method permit the isolation of a defined DNA sequence from a large and complex genome.

Keywords: RNA-cellulose, simian virus 40, Escherichia coli, gene integration, RNA-DNA hybridization

Full text

PDF
1697

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Astell C., Smith M. Thermal elution of complementary sequences of nucleic acids from cellulose columns with covalently attached oligonucleotides of known length and sequence. J Biol Chem. 1971 Mar 25;246(6):1944–1946. [PubMed] [Google Scholar]
  2. 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 Jun;69(6):1408–1412. doi: 10.1073/pnas.69.6.1408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bonner J., Kung G., Bekhor I. A method for the hybridization of nucleic acid molecules at low temperature. Biochemistry. 1967 Dec;6(12):3650–3653. doi: 10.1021/bi00864a005. [DOI] [PubMed] [Google Scholar]
  4. Brenner D. J., Fournier M. J., Doctor B. P. Isolation and partial characterization of the transfer ribonucleic acid cistrons from Escherichia coli. Nature. 1970 Aug 1;227(5257):448–451. doi: 10.1038/227448a0. [DOI] [PubMed] [Google Scholar]
  5. Britten R. J., Kohne D. E. Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms. Science. 1968 Aug 9;161(3841):529–540. doi: 10.1126/science.161.3841.529. [DOI] [PubMed] [Google Scholar]
  6. CHAMBERLIN M., BERG P. Deoxyribo ucleic acid-directed synthesis of ribonucleic acid by an enzyme from Escherichia coli. Proc Natl Acad Sci U S A. 1962 Jan 15;48:81–94. doi: 10.1073/pnas.48.1.81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. CRAWFORD L. V., BLACK P. H. THE NUCLEIC ACID OF SIMIAN VIRUS 40. Virology. 1964 Nov;24:388–392. doi: 10.1016/0042-6822(64)90176-x. [DOI] [PubMed] [Google Scholar]
  8. Daniel V., Beckmann J. S., Sarid S., Grimberg J. I., Herzberg M., Littauer U. Z. Purification and in vitro transcription of a transfer RNA gene. Proc Natl Acad Sci U S A. 1971 Sep;68(9):2268–2272. doi: 10.1073/pnas.68.9.2268. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Edmonds M., Caramela M. G. The isolation and characterization of adenosine monophosphate-rich polynucleotides synthesized by Ehrlich ascites cells. J Biol Chem. 1969 Mar 10;244(5):1314–1324. [PubMed] [Google Scholar]
  10. Gelb L. D., Aaronson S. A., Martin M. A. Heterogeneity of murine leukemia virus in vitro DNA; detection of viral DNA in mammalian cells. Science. 1971 Jun 25;172(3990):1353–1355. doi: 10.1126/science.172.3990.1353. [DOI] [PubMed] [Google Scholar]
  11. Gelb L. D., Kohne D. E., Martin M. A. Quantitation of Simian virus 40 sequences in African green monkey, mouse and virus-transformed cell genomes. J Mol Biol. 1971 Apr 14;57(1):129–145. doi: 10.1016/0022-2836(71)90123-9. [DOI] [PubMed] [Google Scholar]
  12. Kitos P. A., Saxon G., Amos H. The isolation of polyadenylate with unreacted cellulose. Biochem Biophys Res Commun. 1972 Jun 28;47(6):1426–1437. doi: 10.1016/0006-291x(72)90232-x. [DOI] [PubMed] [Google Scholar]
  13. Kohne D. E. Isolation and characterization of bacterial ribosomal RNA cistrons. Biophys J. 1968 Oct;8(10):1104–1118. doi: 10.1016/S0006-3495(68)86542-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Martin M. A., Axelrod D. SV40 gene activity during lytic infection and in a series of SV40 transformed mouse cells. Proc Natl Acad Sci U S A. 1969 Dec;64(4):1203–1210. doi: 10.1073/pnas.64.4.1203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Radloff R., Bauer W., Vinograd J. A dye-buoyant-density method for the detection and isolation of closed circular duplex DNA: the closed circular DNA in HeLa cells. Proc Natl Acad Sci U S A. 1967 May;57(5):1514–1521. doi: 10.1073/pnas.57.5.1514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ryan J. L., Morowitz H. J. Partial purification of native rRNA and tRNA cistrons from mycoplasma sp. (Kid). Proc Natl Acad Sci U S A. 1969 Aug;63(4):1282–1289. doi: 10.1073/pnas.63.4.1282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sambrook J., Westphal H., Srinivasan P. R., Dulbecco R. The integrated state of viral DNA in SV40-transformed cells. Proc Natl Acad Sci U S A. 1968 Aug;60(4):1288–1295. doi: 10.1073/pnas.60.4.1288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Schmeckpeper B. J., Smith K. D. Use of formamide in nucleic acid reassociation. Biochemistry. 1972 Mar 28;11(7):1319–1326. doi: 10.1021/bi00757a032. [DOI] [PubMed] [Google Scholar]
  19. Sgaramella V., Spadari S., Falaschi A. Isolation of the hybrid between ribosomal RNA and DNA of Bacillus subtilis. Cold Spring Harb Symp Quant Biol. 1968;33:839–842. doi: 10.1101/sqb.1968.033.01.095. [DOI] [PubMed] [Google Scholar]
  20. Shapiro J., Machattie L., Eron L., Ihler G., Ippen K., Beckwith J. Isolation of pure lac operon DNA. Nature. 1969 Nov 22;224(5221):768–774. doi: 10.1038/224768a0. [DOI] [PubMed] [Google Scholar]
  21. Shih T. Y., Bonner J. Template properties of DNA-polypeptide complexes. J Mol Biol. 1970 Jun 14;50(2):333–344. doi: 10.1016/0022-2836(70)90196-8. [DOI] [PubMed] [Google Scholar]
  22. Trilling D. M., Axelrod D. Encapsidation of free host DNA by simian virus 40: a simian virus 40 pseudovirus. Science. 1970 Apr 10;168(3928):268–271. doi: 10.1126/science.168.3928.268. [DOI] [PubMed] [Google Scholar]
  23. Varmus H. E., Weiss R. A., Friis R. R., Levinson W., Bishop J. M. Detection of avian tumor virus-specific nucleotide sequences in avian cell DNAs (reassociation kinetics-RNA tumor viruses-gas antigen-Rous sarcoma virus, chick cells). Proc Natl Acad Sci U S A. 1972 Jan;69(1):20–24. doi: 10.1073/pnas.69.1.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Wetmur J. G., Davidson N. Kinetics of renaturation of DNA. J Mol Biol. 1968 Feb 14;31(3):349–370. doi: 10.1016/0022-2836(68)90414-2. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES