Skip to main content
Log in

Southwestern blotting in investigating transcriptional regulation

  • Protocol
  • Published:

From Nature Protocols

View current issue Submit your manuscript

Abstract

Southwestern blotting is used to investigate DNA–protein interactions. The advantage of this technique over other related methods such as electrophoretic mobility shift assay (EMSA) and DNA footprinting is that it provides information regarding the molecular weight of unknown protein factor. This method combines the features of Southern and Western blotting techniques; a denaturing SDS-PAGE is first employed to separate proteins electrophoretically based on size, and after transferring the proteins to a membrane support, the membrane-bound proteins are renatured and incubated with a 32P-labeled double-stranded oligonucleotide probe of specific DNA sequence. The interaction of the probe with the protein(s) is later visualized by autoradiography. This technique could be combined with database searching (TransFac, http://www.gene-regulation.com/pub/databases.html#transfac), prediction of potential protein factors binding onto a target motif (e.g., Patch search), in vitro supershift EMSA and in vivo chromatin immunoprecipitation (ChIP) assays for effective identification of protein factors. The whole Southwestern blotting procedure takes ∼4 d to complete. In this article, a commonly used protocol and expected results are described and discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1: A flow chart summarizing the approximate time needed and the procedures involved in Southwestern blotting.
Figure 2: A flow chart showing a strategy for identifying DNA-binding proteins (e.g., transcription factors) by Southwestern blotting in combination with other methods.
Figure 3: Southwestern blotting of the N1 motif with SH-SY5Y nuclear extracts.

Similar content being viewed by others

References

  1. Bowen, B., Steinberg, J., Laemmli, U.K. & Weintraub, H. The detection of DNA-binding proteins by protein blotting. Nucleic Acids Res. 8, 1–20 (1980).

    Article  CAS  Google Scholar 

  2. Jack, R.S., Gehring, W.J. & Brack, C. Protein component from Drosophila larval nuclei showing sequence specificity for a short region near a major heat-shock protein gene. Cell 24, 321–331 (1981).

    Article  CAS  Google Scholar 

  3. Anachkova, B. & Russev, G. Differential binding of nonhistone chromosomal proteins to the putative mouse origin of replication. Biochim. Biophys. Acta 740, 369–372 (1983).

    Article  CAS  Google Scholar 

  4. Triadou, P., Crepin, M., Gros, F. & Lelong, J.C. Tissue-specific binding of total and beta-globin genomic deoxyribonucleic acid to non-histone chromosomal proteins from mouse erythropoietic cells. Biochemistry 21, 6060–6065 (1982).

    Article  CAS  Google Scholar 

  5. Watt, R.A., Shatzman, A.R. & Rosenberg, M. Expression and characterization of the human c-myc DNA-binding protein. Mol. Cell Biol. 5, 448–456 (1985).

    Article  CAS  Google Scholar 

  6. Miskimins, W.K., Roberts, M.P., McClelland, A. & Ruddle, F.H. Use of a protein-blotting procedure and a specific DNA probe to identify nuclear proteins that recognize the promoter region of the transferrin receptor gene. Proc. Natl. Acad. Sci. USA 82, 6741–6744 (1985).

    Article  CAS  Google Scholar 

  7. Cheng, C.K., Yeung, C.M., Hoo, R.L., Chow, B.K. & Leung, P.C. Oct-1 is involved in the transcriptional repression of the gonadotropin-releasing hormone receptor gene. Endocrinology 143, 4693–4701 (2002).

    Article  CAS  Google Scholar 

  8. Lee, L.T., Tan-Un, K.C., Lin, M.C. & Chow, B.K. Retinoic acid activates human secretin gene expression by Sp proteins and nuclear factor I in neuronal SH-SY5Y cells. J. Neurochem. 93, 339–350 (2005).

    Article  CAS  Google Scholar 

  9. Hellman, L.M. & Fried, M.G. Electrophoretic mobility shift assay (EMSA) for detecting protein-nucleic acid interactions. Nat. Protoc. 2, 1849–1861 (2007).

    Article  CAS  Google Scholar 

  10. Matys, V. et al. TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes. Nucleic Acids Res. 34, D108–D110 (2006).

    Article  CAS  Google Scholar 

  11. Chekmenev, D.S., Haid, C. & Kel, A.E. P-Match: transcription factor binding site search by combining patterns and weight matrices. Nucleic Acids Res. 33, W432–W437 (2005).

    Article  CAS  Google Scholar 

  12. Bradford, M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248–254 (1976).

    Article  CAS  Google Scholar 

  13. Lowry, O.H., Rosebrough, N.J., Farr, A.L. & Randall, R.J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265–275 (1951).

    CAS  PubMed  Google Scholar 

  14. Lee, K.A., Bindereif, A. & Green, M.R. A small-scale procedure for preparation of nuclear extracts that support efficient transcription and pre-mRNA splicing. Gene Anal. Tech. 5, 22–31 (1988).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The work was supported by Hong Kong Government RGC Grants HKU7501/05M, HKU7639/07M to B.K.C.C.

Author information

Authors and Affiliations

Authors

Contributions

F.K.Y.S. and L.T.O.L. contributed equally to this work, and should be considered as cofirst authors.

Corresponding author

Correspondence to Billy K C Chow.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Siu, F., Lee, L. & Chow, B. Southwestern blotting in investigating transcriptional regulation. Nat Protoc 3, 51–58 (2008). https://doi.org/10.1038/nprot.2007.492

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nprot.2007.492

  • Springer Nature Limited

This article is cited by

Navigation