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. 1995 Oct;177(19):5612–5621. doi: 10.1128/jb.177.19.5612-5621.1995

Mutations in motif II of Escherichia coli DNA helicase II render the enzyme nonfunctional in both mismatch repair and excision repair with differential effects on the unwinding reaction.

R M Brosh Jr 1, S W Matson 1
PMCID: PMC177372  PMID: 7559350

Abstract

Site-directed mutagenesis has been employed to address the functional significance of the highly conserved aspartic and glutamic acid residues present in the Walker B (also called motif II) sequence in Escherichia coli DNA helicase II. Two mutant proteins, UvrDE221Q and UvrDD220NE221Q, were expressed and purified to apparent homogeneity. Biochemical characterization of the DNA-dependent ATPase activity of each mutant protein demonstrated a kcat that was < 0.5% of that of the wild-type protein, with no significant change in the apparent Km for ATP. The E221Q mutant protein exhibited no detectable unwinding of either partial duplex or blunt duplex DNA substrates. The D220NE221Q mutant, however, catalyzed unwinding of both partial duplex and blunt duplex substrates, but at a greatly reduced rate compared with that of the wild-type enzyme. Both mutants were able to bind DNA. Thus, the motif II mutants E221Q and D220NE221Q were able to bind ATP and DNA to the same extent as wild-type helicase II but demonstrate a significant reduction in ATP hydrolysis and helicase functions. The mutant uvrD alleles were also characterized by examining their abilities to complement the mutator and UV light-sensitive phenotypes of a uvrD deletion mutant. Neither the uvrDE221Q nor the uvrDD220NE221Q allele, supplied on a plasmid, was able to complement either phenotype. Further genetic characterization of the mutant uvrD alleles demonstrated that uvrDE221Q confers a dominant negative growth phenotype; the uvrDD220NE221Q allele does not exhibit this effect. The observed difference in effect on viability may reflect the gene products' dissimilar kinetics for unwinding duplex DNA substrates in vitro.

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Selected References

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  1. Abdel-Monem M., Dürwald H., Hoffmann-Berling H. DNA unwinding enzyme II of Escherichia coli. 2. Characterization of the DNA unwinding activity. Eur J Biochem. 1977 Sep 15;79(1):39–45. doi: 10.1111/j.1432-1033.1977.tb11781.x. [DOI] [PubMed] [Google Scholar]
  2. Arthur H. M., Lloyd R. G. Hyper-recombination in uvrD mutants of Escherichia coli K-12. Mol Gen Genet. 1980;180(1):185–191. doi: 10.1007/BF00267368. [DOI] [PubMed] [Google Scholar]
  3. Bridges B. A., von Wright A. Influence of mutations at the rep gene on survival of Escherichia coli following ultraviolet light irradiation or 8-methoxypsoralen photosensitization: evidence for a recA+ rep+-dependent pathway for repair of DNA crosslinks. Mutat Res. 1981 Jul;82(2):229–238. doi: 10.1016/0027-5107(81)90152-4. [DOI] [PubMed] [Google Scholar]
  4. Caron P. R., Kushner S. R., Grossman L. Involvement of helicase II (uvrD gene product) and DNA polymerase I in excision mediated by the uvrABC protein complex. Proc Natl Acad Sci U S A. 1985 Aug;82(15):4925–4929. doi: 10.1073/pnas.82.15.4925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Feinstein S. I., Low K. B. Hyper-recombining recipient strains in bacterial conjugation. Genetics. 1986 May;113(1):13–33. doi: 10.1093/genetics/113.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fry D. C., Kuby S. A., Mildvan A. S. ATP-binding site of adenylate kinase: mechanistic implications of its homology with ras-encoded p21, F1-ATPase, and other nucleotide-binding proteins. Proc Natl Acad Sci U S A. 1986 Feb;83(4):907–911. doi: 10.1073/pnas.83.4.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. George J. W., Brosh R. M., Jr, Matson S. W. A dominant negative allele of the Escherichia coli uvrD gene encoding DNA helicase II. A biochemical and genetic characterization. J Mol Biol. 1994 Jan 14;235(2):424–435. doi: 10.1006/jmbi.1994.1003. [DOI] [PubMed] [Google Scholar]
  8. Gorbalenya A. E., Koonin E. V., Donchenko A. P., Blinov V. M. A novel superfamily of nucleoside triphosphate-binding motif containing proteins which are probably involved in duplex unwinding in DNA and RNA replication and recombination. FEBS Lett. 1988 Aug 1;235(1-2):16–24. doi: 10.1016/0014-5793(88)81226-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gorbalenya A. E., Koonin E. V. Superfamily of UvrA-related NTP-binding proteins. Implications for rational classification of recombination/repair systems. J Mol Biol. 1990 Jun 20;213(4):583–591. doi: 10.1016/S0022-2836(05)80243-8. [DOI] [PubMed] [Google Scholar]
  10. Grilley M., Holmes J., Yashar B., Modrich P. Mechanisms of DNA-mismatch correction. Mutat Res. 1990 Sep-Nov;236(2-3):253–267. doi: 10.1016/0921-8777(90)90009-t. [DOI] [PubMed] [Google Scholar]
  11. Hodgman T. C. A new superfamily of replicative proteins. Nature. 1988 May 5;333(6168):22–23. doi: 10.1038/333022b0. [DOI] [PubMed] [Google Scholar]
  12. Horii Z., Clark A. J. Genetic analysis of the recF pathway to genetic recombination in Escherichia coli K12: isolation and characterization of mutants. J Mol Biol. 1973 Oct 25;80(2):327–344. doi: 10.1016/0022-2836(73)90176-9. [DOI] [PubMed] [Google Scholar]
  13. Husain I., Van Houten B., Thomas D. C., Abdel-Monem M., Sancar A. Effect of DNA polymerase I and DNA helicase II on the turnover rate of UvrABC excision nuclease. Proc Natl Acad Sci U S A. 1985 Oct;82(20):6774–6778. doi: 10.1073/pnas.82.20.6774. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Jindal H. K., Yong C. B., Wilson G. M., Tam P., Astell C. R. Mutations in the NTP-binding motif of minute virus of mice (MVM) NS-1 protein uncouple ATPase and DNA helicase functions. J Biol Chem. 1994 Feb 4;269(5):3283–3289. [PubMed] [Google Scholar]
  15. Kuhn B., Abdel-Monem M., Krell H., Hoffmann-Berling H. Evidence for two mechanisms for DNA unwinding catalyzed by DNA helicases. J Biol Chem. 1979 Nov 25;254(22):11343–11350. [PubMed] [Google Scholar]
  16. Kunkel T. A., Bebenek K., McClary J. Efficient site-directed mutagenesis using uracil-containing DNA. Methods Enzymol. 1991;204:125–139. doi: 10.1016/0076-6879(91)04008-c. [DOI] [PubMed] [Google Scholar]
  17. Lahue R. S., Au K. G., Modrich P. DNA mismatch correction in a defined system. Science. 1989 Jul 14;245(4914):160–164. doi: 10.1126/science.2665076. [DOI] [PubMed] [Google Scholar]
  18. Lechner R. L., Richardson C. C. A preformed, topologically stable replication fork. Characterization of leading strand DNA synthesis catalyzed by T7 DNA polymerase and T7 gene 4 protein. J Biol Chem. 1983 Sep 25;258(18):11185–11196. [PubMed] [Google Scholar]
  19. Lohman T. M. Escherichia coli DNA helicases: mechanisms of DNA unwinding. Mol Microbiol. 1992 Jan;6(1):5–14. doi: 10.1111/j.1365-2958.1992.tb00831.x. [DOI] [PubMed] [Google Scholar]
  20. Lohman T. M. Helicase-catalyzed DNA unwinding. J Biol Chem. 1993 Feb 5;268(4):2269–2272. [PubMed] [Google Scholar]
  21. Maples V. F., Kushner S. R. DNA repair in Escherichia coli: identification of the uvrD gene product. Proc Natl Acad Sci U S A. 1982 Sep;79(18):5616–5620. doi: 10.1073/pnas.79.18.5616. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Matson S. W., Bean D. W., George J. W. DNA helicases: enzymes with essential roles in all aspects of DNA metabolism. Bioessays. 1994 Jan;16(1):13–22. doi: 10.1002/bies.950160103. [DOI] [PubMed] [Google Scholar]
  23. Matson S. W. Escherichia coli DNA helicase II (uvrD gene product) catalyzes the unwinding of DNA.RNA hybrids in vitro. Proc Natl Acad Sci U S A. 1989 Jun;86(12):4430–4434. doi: 10.1073/pnas.86.12.4430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Matson S. W. Escherichia coli helicase II (urvD gene product) translocates unidirectionally in a 3' to 5' direction. J Biol Chem. 1986 Aug 5;261(22):10169–10175. [PubMed] [Google Scholar]
  25. Matson S. W., Kaiser-Rogers K. A. DNA helicases. Annu Rev Biochem. 1990;59:289–329. doi: 10.1146/annurev.bi.59.070190.001445. [DOI] [PubMed] [Google Scholar]
  26. Matson S. W., Richardson C. C. DNA-dependent nucleoside 5'-triphosphatase activity of the gene 4 protein of bacteriophage T7. J Biol Chem. 1983 Nov 25;258(22):14009–14016. [PubMed] [Google Scholar]
  27. Matson S. W., Richardson C. C. Nucleotide-dependent binding of the gene 4 protein of bacteriophage T7 to single-stranded DNA. J Biol Chem. 1985 Feb 25;260(4):2281–2287. [PubMed] [Google Scholar]
  28. Mendonca V. M., Kaiser-Rogers K., Matson S. W. Double helicase II (uvrD)-helicase IV (helD) deletion mutants are defective in the recombination pathways of Escherichia coli. J Bacteriol. 1993 Aug;175(15):4641–4651. doi: 10.1128/jb.175.15.4641-4651.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Modrich P. Methyl-directed DNA mismatch correction. J Biol Chem. 1989 Apr 25;264(12):6597–6600. [PubMed] [Google Scholar]
  30. Morel P., Hejna J. A., Ehrlich S. D., Cassuto E. Antipairing and strand transferase activities of E. coli helicase II (UvrD). Nucleic Acids Res. 1993 Jul 11;21(14):3205–3209. doi: 10.1093/nar/21.14.3205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Orren D. K., Selby C. P., Hearst J. E., Sancar A. Post-incision steps of nucleotide excision repair in Escherichia coli. Disassembly of the UvrBC-DNA complex by helicase II and DNA polymerase I. J Biol Chem. 1992 Jan 15;267(2):780–788. [PubMed] [Google Scholar]
  32. Ossanna N., Mount D. W. Mutations in uvrD induce the SOS response in Escherichia coli. J Bacteriol. 1989 Jan;171(1):303–307. doi: 10.1128/jb.171.1.303-307.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Pause A., Sonenberg N. Mutational analysis of a DEAD box RNA helicase: the mammalian translation initiation factor eIF-4A. EMBO J. 1992 Jul;11(7):2643–2654. doi: 10.1002/j.1460-2075.1992.tb05330.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Richet E., Kohiyama M. Purification and characterization of a DNA-dependent ATPase from Escherichia coli. J Biol Chem. 1976 Feb 10;251(3):808–812. [PubMed] [Google Scholar]
  35. Runyon G. T., Bear D. G., Lohman T. M. Escherichia coli helicase II (UvrD) protein initiates DNA unwinding at nicks and blunt ends. Proc Natl Acad Sci U S A. 1990 Aug;87(16):6383–6387. doi: 10.1073/pnas.87.16.6383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Runyon G. T., Lohman T. M. Escherichia coli helicase II (uvrD) protein can completely unwind fully duplex linear and nicked circular DNA. J Biol Chem. 1989 Oct 15;264(29):17502–17512. [PubMed] [Google Scholar]
  37. Runyon G. T., Wong I., Lohman T. M. Overexpression, purification, DNA binding, and dimerization of the Escherichia coli uvrD gene product (helicase II). Biochemistry. 1993 Jan 19;32(2):602–612. doi: 10.1021/bi00053a028. [DOI] [PubMed] [Google Scholar]
  38. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Sargentini N. J., Smith K. C. Involvement of genes uvrD and recB in separate mutagenic deoxyribonucleic acid repair pathways in Escherichia coli K-12 uvrB5 and B/r uvrA155. J Bacteriol. 1980 Jul;143(1):212–220. doi: 10.1128/jb.143.1.212-220.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Siegel E. C., Race H. M. Phenotypes of UV-sensitive uvrD3, recL152, and uvrE15 mutants of Escherichia coli. Mutat Res. 1981 Aug;83(1):49–59. doi: 10.1016/0027-5107(81)90070-1. [DOI] [PubMed] [Google Scholar]
  41. Walker J. E., Saraste M., Runswick M. J., Gay N. J. Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold. EMBO J. 1982;1(8):945–951. doi: 10.1002/j.1460-2075.1982.tb01276.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Washburn B. K., Kushner S. R. Characterization of DNA helicase II from a uvrD252 mutant of Escherichia coli. J Bacteriol. 1993 Jan;175(2):341–350. doi: 10.1128/jb.175.2.341-350.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Washburn B. K., Kushner S. R. Construction and analysis of deletions in the structural gene (uvrD) for DNA helicase II of Escherichia coli. J Bacteriol. 1991 Apr;173(8):2569–2575. doi: 10.1128/jb.173.8.2569-2575.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Wong I., Amaratunga M., Lohman T. M. Heterodimer formation between Escherichia coli Rep and UvrD proteins. J Biol Chem. 1993 Sep 25;268(27):20386–20391. [PubMed] [Google Scholar]
  45. Youngs D. A., Smith K. C. Genetic control of multiple pathways of post-replicational repair in uvrB strains of Escherichia coli K-12. J Bacteriol. 1976 Jan;125(1):102–110. doi: 10.1128/jb.125.1.102-110.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]

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