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. 1996 Jul 1;24(13):2567–2574. doi: 10.1093/nar/24.13.2567

Assessment of major and minor groove DNA interactions by the zinc fingers of Xenopus transcription factor IIIA.

S J McBryant 1, B Gedulin 1, K R Clemens 1, P E Wright 1, J M Gottesfeld 1
PMCID: PMC145982  PMID: 8692697

Abstract

Zinc finger proteins of the Cys2His2 class are DNA sequence-specific transcription factors. Previous structural studies of zinc finger protein-DNA complexes have shown that amino acids in the finger tip and alpha-helix regions within individual finger domains make base-specific contacts with the major groove of DNA. The nine finger protein transcription factor IIIA (TFIIIA) from Xenopus oocytes binds a 43 base pair region of the 5S RNA gene through major groove interactions with two sets of three fingers (fingers 1-3 and 7-9) and with finger 5. Previous studies have suggested that zinc fingers 4 and 6 each bind in or across the minor groove to bridge these major groove-binding zinc fingers. Here it is shown that a polypeptide containing zinc fingers 1-5 (zf1-5) binds oligonucleotides with modifications in the major groove of the finger 4 binding site with wild-type affinity. Mutagenesis and binding site selection studies were performed to determine whether high affinity DNA binding by zf1-5 requires a particular sequence in the binding site for finger 4. Several mutations in this region of the 5S gene reduced the DNA-binding affinity of zf1-5; however, selection and amplification binding assays did not recover the wild-type finger 4 binding site sequence from a pool of mixed sequence oligonucleotides. Rather, a purine-rich sequence on the top strand was highly selected within the finger 4 binding site. We suggest that high affinity DNA binding by zinc finger 4 may be dictated by a sequence-specific DNA structure rather than by a unique DNA sequence. Deletion of finger 4 from zf1-5 results in a protein with poor binding affinity, demonstrating the importance of finger 4 in proper alignment of neighboring fingers with the DNA, and/or the importance of correct protein-protein interactions between fingers.

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Selected References

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

  1. Blackwell T. K., Weintraub H. Differences and similarities in DNA-binding preferences of MyoD and E2A protein complexes revealed by binding site selection. Science. 1990 Nov 23;250(4984):1104–1110. doi: 10.1126/science.2174572. [DOI] [PubMed] [Google Scholar]
  2. Bogenhagen D. F., Sakonju S., Brown D. D. A control region in the center of the 5S RNA gene directs specific initiation of transcription: II. The 3' border of the region. Cell. 1980 Jan;19(1):27–35. doi: 10.1016/0092-8674(80)90385-2. [DOI] [PubMed] [Google Scholar]
  3. Choo Y., Klug A. Selection of DNA binding sites for zinc fingers using rationally randomized DNA reveals coded interactions. Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):11168–11172. doi: 10.1073/pnas.91.23.11168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Choo Y., Klug A. Toward a code for the interactions of zinc fingers with DNA: selection of randomized fingers displayed on phage. Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):11163–11167. doi: 10.1073/pnas.91.23.11163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Christensen J. H., Hansen P. K., Lillelund O., Thøgersen H. C. Sequence-specific binding of the N-terminal three-finger fragment of Xenopus transcription factor IIIA to the internal control region of a 5S RNA gene. FEBS Lett. 1991 Apr 9;281(1-2):181–184. doi: 10.1016/0014-5793(91)80388-j. [DOI] [PubMed] [Google Scholar]
  6. Churchill M. E., Tullius T. D., Klug A. Mode of interaction of the zinc finger protein TFIIIA with a 5S RNA gene of Xenopus. Proc Natl Acad Sci U S A. 1990 Jul;87(14):5528–5532. doi: 10.1073/pnas.87.14.5528. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Clemens K. R., Liao X., Wolf V., Wright P. E., Gottesfeld J. M. Definition of the binding sites of individual zinc fingers in the transcription factor IIIA-5S RNA gene complex. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10822–10826. doi: 10.1073/pnas.89.22.10822. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Clemens K. R., Wolf V., McBryant S. J., Zhang P., Liao X., Wright P. E., Gottesfeld J. M. Molecular basis for specific recognition of both RNA and DNA by a zinc finger protein. Science. 1993 Apr 23;260(5107):530–533. doi: 10.1126/science.8475383. [DOI] [PubMed] [Google Scholar]
  9. Clemens K. R., Zhang P., Liao X., McBryant S. J., Wright P. E., Gottesfeld J. M. Relative contributions of the zinc fingers of transcription factor IIIA to the energetics of DNA binding. J Mol Biol. 1994 Nov 18;244(1):23–35. doi: 10.1006/jmbi.1994.1701. [DOI] [PubMed] [Google Scholar]
  10. Del Rio S., Menezes S. R., Setzer D. R. The function of individual zinc fingers in sequence-specific DNA recognition by transcription factor IIIA. J Mol Biol. 1993 Oct 20;233(4):567–579. doi: 10.1006/jmbi.1993.1536. [DOI] [PubMed] [Google Scholar]
  11. Engelke D. R., Ng S. Y., Shastry B. S., Roeder R. G. Specific interaction of a purified transcription factor with an internal control region of 5S RNA genes. Cell. 1980 Mar;19(3):717–728. doi: 10.1016/s0092-8674(80)80048-1. [DOI] [PubMed] [Google Scholar]
  12. Fairall L., Rhodes D., Klug A. Mapping of the sites of protection on a 5 S RNA gene by the Xenopus transcription factor IIIA. A model for the interaction. J Mol Biol. 1986 Dec 5;192(3):577–591. doi: 10.1016/0022-2836(86)90278-0. [DOI] [PubMed] [Google Scholar]
  13. Fairall L., Schwabe J. W., Chapman L., Finch J. T., Rhodes D. The crystal structure of a two zinc-finger peptide reveals an extension to the rules for zinc-finger/DNA recognition. Nature. 1993 Dec 2;366(6454):483–487. doi: 10.1038/366483a0. [DOI] [PubMed] [Google Scholar]
  14. Ginsberg A. M., King B. O., Roeder R. G. Xenopus 5S gene transcription factor, TFIIIA: characterization of a cDNA clone and measurement of RNA levels throughout development. Cell. 1984 Dec;39(3 Pt 2):479–489. doi: 10.1016/0092-8674(84)90455-0. [DOI] [PubMed] [Google Scholar]
  15. Hayes J. J., Clemens K. R. Locations of contacts between individual zinc fingers of Xenopus laevis transcription factor IIIA and the internal control region of a 5S RNA gene. Biochemistry. 1992 Nov 24;31(46):11600–11605. doi: 10.1021/bi00161a045. [DOI] [PubMed] [Google Scholar]
  16. Hayes J. J., Tullius T. D. Structure of the TFIIIA-5 S DNA complex. J Mol Biol. 1992 Sep 20;227(2):407–417. doi: 10.1016/0022-2836(92)90897-s. [DOI] [PubMed] [Google Scholar]
  17. Honda B. M., Roeder R. G. Association of a 5S gene transcription factor with 5S RNA and altered levels of the factor during cell differentiation. Cell. 1980 Nov;22(1 Pt 1):119–126. doi: 10.1016/0092-8674(80)90160-9. [DOI] [PubMed] [Google Scholar]
  18. Hughes K. T., Gaines P. C., Karlinsey J. E., Vinayak R., Simon M. I. Sequence-specific interaction of the Salmonella Hin recombinase in both major and minor grooves of DNA. EMBO J. 1992 Jul;11(7):2695–2705. doi: 10.1002/j.1460-2075.1992.tb05335.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Jacobs G. H. Determination of the base recognition positions of zinc fingers from sequence analysis. EMBO J. 1992 Dec;11(12):4507–4517. doi: 10.1002/j.1460-2075.1992.tb05552.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Jamieson A. C., Kim S. H., Wells J. A. In vitro selection of zinc fingers with altered DNA-binding specificity. Biochemistry. 1994 May 17;33(19):5689–5695. doi: 10.1021/bi00185a004. [DOI] [PubMed] [Google Scholar]
  21. Lee M. S., Gippert G. P., Soman K. V., Case D. A., Wright P. E. Three-dimensional solution structure of a single zinc finger DNA-binding domain. Science. 1989 Aug 11;245(4918):635–637. doi: 10.1126/science.2503871. [DOI] [PubMed] [Google Scholar]
  22. Liao X. B., Clemens K. R., Tennant L., Wright P. E., Gottesfeld J. M. Specific interaction of the first three zinc fingers of TFIIIA with the internal control region of the Xenopus 5 S RNA gene. J Mol Biol. 1992 Feb 20;223(4):857–871. doi: 10.1016/0022-2836(92)90248-i. [DOI] [PubMed] [Google Scholar]
  23. Miller J., McLachlan A. D., Klug A. Repetitive zinc-binding domains in the protein transcription factor IIIA from Xenopus oocytes. EMBO J. 1985 Jun;4(6):1609–1614. doi: 10.1002/j.1460-2075.1985.tb03825.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Omichinski J. G., Clore G. M., Appella E., Sakaguchi K., Gronenborn A. M. High-resolution three-dimensional structure of a single zinc finger from a human enhancer binding protein in solution. Biochemistry. 1990 Oct 9;29(40):9324–9334. doi: 10.1021/bi00492a004. [DOI] [PubMed] [Google Scholar]
  25. Pavletich N. P., Pabo C. O. Crystal structure of a five-finger GLI-DNA complex: new perspectives on zinc fingers. Science. 1993 Sep 24;261(5129):1701–1707. doi: 10.1126/science.8378770. [DOI] [PubMed] [Google Scholar]
  26. Pavletich N. P., Pabo C. O. Zinc finger-DNA recognition: crystal structure of a Zif268-DNA complex at 2.1 A. Science. 1991 May 10;252(5007):809–817. doi: 10.1126/science.2028256. [DOI] [PubMed] [Google Scholar]
  27. Pieler T., Hamm J., Roeder R. G. The 5S gene internal control region is composed of three distinct sequence elements, organized as two functional domains with variable spacing. Cell. 1987 Jan 16;48(1):91–100. doi: 10.1016/0092-8674(87)90359-x. [DOI] [PubMed] [Google Scholar]
  28. Pieler T., Oei S. L., Hamm J., Engelke U., Erdmann V. A. Functional domains of the Xenopus laevis 5S gene promoter. EMBO J. 1985 Dec 30;4(13B):3751–3756. doi: 10.1002/j.1460-2075.1985.tb04144.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Rebar E. J., Pabo C. O. Zinc finger phage: affinity selection of fingers with new DNA-binding specificities. Science. 1994 Feb 4;263(5147):671–673. doi: 10.1126/science.8303274. [DOI] [PubMed] [Google Scholar]
  30. Romaniuk P. J. Characterization of the equilibrium binding of Xenopus transcription factor IIIA to the 5 S RNA gene. J Biol Chem. 1990 Oct 15;265(29):17593–17600. [PubMed] [Google Scholar]
  31. Sakonju S., Bogenhagen D. F., Brown D. D. A control region in the center of the 5S RNA gene directs specific initiation of transcription: I. The 5' border of the region. Cell. 1980 Jan;19(1):13–25. doi: 10.1016/0092-8674(80)90384-0. [DOI] [PubMed] [Google Scholar]
  32. Sakonju S., Brown D. D. Contact points between a positive transcription factor and the Xenopus 5S RNA gene. Cell. 1982 Dec;31(2 Pt 1):395–405. doi: 10.1016/0092-8674(82)90133-7. [DOI] [PubMed] [Google Scholar]
  33. Smith D. R., Jackson I. J., Brown D. D. Domains of the positive transcription factor specific for the Xenopus 5S RNA gene. Cell. 1984 Jun;37(2):645–652. doi: 10.1016/0092-8674(84)90396-9. [DOI] [PubMed] [Google Scholar]
  34. Starr D. B., Hawley D. K. TFIID binds in the minor groove of the TATA box. Cell. 1991 Dec 20;67(6):1231–1240. doi: 10.1016/0092-8674(91)90299-e. [DOI] [PubMed] [Google Scholar]
  35. Veldhoen N., You Q., Setzer D. R., Romaniuk P. J. Contribution of individual base pairs to the interaction of TFIIIA with the Xenopus 5S RNA gene. Biochemistry. 1994 Jun 21;33(24):7568–7575. doi: 10.1021/bi00190a009. [DOI] [PubMed] [Google Scholar]
  36. Vrana K. E., Churchill M. E., Tullius T. D., Brown D. D. Mapping functional regions of transcription factor TFIIIA. Mol Cell Biol. 1988 Apr;8(4):1684–1696. doi: 10.1128/mcb.8.4.1684. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Weiss M. A., Keutmann H. T. Alternating zinc finger motifs in the male-associated protein ZFY: defining architectural rules by mutagenesis and design of an "aromatic swap" second-site revertant. Biochemistry. 1990 Oct 23;29(42):9808–9813. doi: 10.1021/bi00494a008. [DOI] [PubMed] [Google Scholar]
  38. Wu H., Yang W. P., Barbas C. F., 3rd Building zinc fingers by selection: toward a therapeutic application. Proc Natl Acad Sci U S A. 1995 Jan 17;92(2):344–348. doi: 10.1073/pnas.92.2.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Xu R. X., Horvath S. J., Klevit R. E. ADR1a, a zinc finger peptide, exists in two folded conformations. Biochemistry. 1991 Apr 9;30(14):3365–3371. doi: 10.1021/bi00228a003. [DOI] [PubMed] [Google Scholar]
  40. You Q. M., Veldhoen N., Baudin F., Romaniuk P. J. Mutations in 5S DNA and 5S RNA have different effects on the binding of Xenopus transcription factor IIIA. Biochemistry. 1991 Mar 5;30(9):2495–2500. doi: 10.1021/bi00223a028. [DOI] [PubMed] [Google Scholar]

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