Abstract
A novel endonuclease has been isolated from extracts of spinach leaves (Spinacia oleracea). The enzyme has been purified by a series of column chromatography steps and has a molecular size of approximately 43,000 daltons. The spinach endonuclease cleaved double stranded DNA damaged by ultraviolet light or cis-diamminedichloroplatinum (II) primarily at sites of adenine when end-labelled DNA fragments of defined sequence were employed as substrates. The nature of the structural distortion contained in damaged, duplex DNA appears to be an important determinant for endonuclease cleavage. DNA helical distortions produced by UV light-induced (6-4) pyrimidine-pyrimidone photoproducts, but not cyclobutane pyrimidine dimers are recognized by the enzyme. The DNA cleavage products generated by the enzyme contain 3'-hydroxyl and 5'-phosphoryl termini. Single stranded DNA and RNA are hydrolyzed by the spinach endonuclease. This enzyme, which we call nuclease SP, is similar in several respects to other single-strand-specific nucleases such as N. crassa and mung bean nucleases and may function in DNA repair and/or recombination events in spinach cells. Nuclease SP should be a useful tool for the analysis of (6-4) photoproducts occurring in duplex DNA.
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- Bailly V., Verly W. G. Escherichia coli endonuclease III is not an endonuclease but a beta-elimination catalyst. Biochem J. 1987 Mar 1;242(2):565–572. doi: 10.1042/bj2420565. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brash D. E., Franklin W. A., Sancar G. B., Sancar A., Haseltine W. A. Escherichia coli DNA photolyase reverses cyclobutane pyrimidine dimers but not pyrimidine-pyrimidone (6-4) photoproducts. J Biol Chem. 1985 Sep 25;260(21):11438–11441. [PubMed] [Google Scholar]
- Carrier W. L., Setlow R. B. Endonuclease from Micrococcus luteus which has activity toward ultraviolet-irradiated deoxyribonucleic acid: purification and properties. J Bacteriol. 1970 Apr;102(1):178–186. doi: 10.1128/jb.102.1.178-186.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chan G. L., Doetsch P. W., Haseltine W. A. Cyclobutane pyrimidine dimers and (6-4) photoproducts block polymerization by DNA polymerase I. Biochemistry. 1985 Oct 8;24(21):5723–5728. doi: 10.1021/bi00342a006. [DOI] [PubMed] [Google Scholar]
- Demple B., Linn S. DNA N-glycosylases and UV repair. Nature. 1980 Sep 18;287(5779):203–208. doi: 10.1038/287203a0. [DOI] [PubMed] [Google Scholar]
- Doetsch P. W., Chan G. L., Haseltine W. A. T4 DNA polymerase (3'-5') exonuclease, an enzyme for the detection and quantitation of stable DNA lesions: the ultraviolet light example. Nucleic Acids Res. 1985 May 10;13(9):3285–3304. doi: 10.1093/nar/13.9.3285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Doetsch P. W., Helland D. E., Haseltine W. A. Mechanism of action of a mammalian DNA repair endonuclease. Biochemistry. 1986 Apr 22;25(8):2212–2220. doi: 10.1021/bi00356a054. [DOI] [PubMed] [Google Scholar]
- Franklin W. A., Doetsch P. W., Haseltine W. A. Structural determination of the ultraviolet light-induced thymine-cytosine pyrimidine-pyrimidone (6-4) photoproduct. Nucleic Acids Res. 1985 Jul 25;13(14):5317–5325. doi: 10.1093/nar/13.14.5317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Franklin W. A., Haseltine W. A. The role of the (6-4) photoproduct in ultraviolet light-induced transition mutations in E. coli. Mutat Res. 1986 Jan;165(1):1–7. doi: 10.1016/0167-8817(86)90002-7. [DOI] [PubMed] [Google Scholar]
- Friedberg E. C., King J. J. Dark repair of ultraviolet-irradiated deoxyribonucleic acid by bacteriophage T4: purification and characterization of a dimer-specific phage-induced endonuclease. J Bacteriol. 1971 May;106(2):500–507. doi: 10.1128/jb.106.2.500-507.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gordon L. K., Haseltine W. A. Quantitation of cyclobutane pyrimidine dimer formation in double- and single-stranded DNA fragments of defined sequence. Radiat Res. 1982 Jan;89(1):99–112. [PubMed] [Google Scholar]
- Holloman W. K., Holliday R. Studies on a nuclease from Ustilago maydis. I. Purification, properties, and implication in recombination of the enzyme. J Biol Chem. 1973 Dec 10;248(23):8107–8113. [PubMed] [Google Scholar]
- Huang W. M., Lehman I. R. On the exonuclease activity of phage T4 deoxyribonucleic acid polymerase. J Biol Chem. 1972 May 25;247(10):3139–3146. [PubMed] [Google Scholar]
- Hutchinson F. A review of some topics concerning mutagenesis by ultraviolet light. Photochem Photobiol. 1987 Jun;45(6):897–903. doi: 10.1111/j.1751-1097.1987.tb07900.x. [DOI] [PubMed] [Google Scholar]
- Johnson P. H., Laskowski M., Sr Mung bean nuclease I. II. Resistance of double stranded deoxyribonucleic acid and susceptibility of regions rich in adenosine and thymidine to enzymatic hydrolysis. J Biol Chem. 1970 Feb 25;245(4):891–898. [PubMed] [Google Scholar]
- Jorgensen T. J., Kow Y. W., Wallace S. S., Henner W. D. Mechanism of action of Micrococcus luteus gamma-endonuclease. Biochemistry. 1987 Oct 6;26(20):6436–6443. doi: 10.1021/bi00394a021. [DOI] [PubMed] [Google Scholar]
- Kato A. C., Fraser M. J. Action of single-strand specific Neurospora crassa endonuclease on ultraviolet light-irradiated native DNA. Biochim Biophys Acta. 1973 Jul 27;312(4):645–655. doi: 10.1016/0005-2787(73)90068-3. [DOI] [PubMed] [Google Scholar]
- Kemmink J., Boelens R., Koning T., van der Marel G. A., van Boom J. H., Kaptein R. 1H NMR study of the exchangeable protons of the duplex d(GCGTTGCG).d(CGCAACGC) containing a thymine photodimer. Nucleic Acids Res. 1987 Jun 11;15(11):4645–4653. doi: 10.1093/nar/15.11.4645. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kowalski D., Kroeker W. D., Laskowski M., Sr Mung bean nuclease I. Physical, chemical, and catalytic properties. Biochemistry. 1976 Oct 5;15(20):4457–4463. doi: 10.1021/bi00665a019. [DOI] [PubMed] [Google Scholar]
- Legerski R. J., Gray H. B., Jr, Robberson D. L. A sensitive endonuclease probe for lesions in deoxyribonucleic acid helix structure produced by carcinogenic or mutagenic agents. J Biol Chem. 1977 Dec 10;252(23):8740–8746. [PubMed] [Google Scholar]
- Lippke J. A., Gordon L. K., Brash D. E., Haseltine W. A. Distribution of UV light-induced damage in a defined sequence of human DNA: detection of alkaline-sensitive lesions at pyrimidine nucleoside-cytidine sequences. Proc Natl Acad Sci U S A. 1981 Jun;78(6):3388–3392. doi: 10.1073/pnas.78.6.3388. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maxam A. M., Gilbert W. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 1980;65(1):499–560. doi: 10.1016/s0076-6879(80)65059-9. [DOI] [PubMed] [Google Scholar]
- Patrick M. H., Gray D. M. Independence of photoproduct formation on DNA conformation. Photochem Photobiol. 1976 Dec;24(6):507–513. doi: 10.1111/j.1751-1097.1976.tb06867.x. [DOI] [PubMed] [Google Scholar]
- Patrick M. H. Studies on thymine-derived UV photoproducts in DNA--I. Formation and biological role of pyrimidine adducts in DNA. Photochem Photobiol. 1977 Apr;25(4):357–372. doi: 10.1111/j.1751-1097.1977.tb07355.x. [DOI] [PubMed] [Google Scholar]
- Pearlman D. A., Holbrook S. R., Pirkle D. H., Kim S. H. Molecular models for DNA damaged by photoreaction. Science. 1985 Mar 15;227(4692):1304–1308. doi: 10.1126/science.3975615. [DOI] [PubMed] [Google Scholar]
- Rao S. N., Keepers J. W., Kollman P. The structure of d(CGCGAAT[]TCGCG) . d(CGCGAATTCGCG); the incorporation of a thymine photodimer into a B-DNA helix. Nucleic Acids Res. 1984 Jun 11;12(11):4789–4807. doi: 10.1093/nar/12.11.4789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rao S. N., Kollman P. A. Conformations of deoxydodecanucleotides with pyrimidine (6-4)-pyrimidone photoadducts. Photochem Photobiol. 1985 Nov;42(5):465–475. doi: 10.1111/j.1751-1097.1985.tb01596.x. [DOI] [PubMed] [Google Scholar]
- Riazuddin S., Grossman L. Micrococcus luteus correndonucleases. I. resolution and purification of two endonucleases specific for DNA containing pyrimidine dimers. J Biol Chem. 1977 Sep 25;252(18):6280–6286. [PubMed] [Google Scholar]
- Sancar A., Sancar G. B. Escherichia coli DNA photolyase is a flavoprotein. J Mol Biol. 1984 Jan 15;172(2):223–227. doi: 10.1016/s0022-2836(84)80040-6. [DOI] [PubMed] [Google Scholar]
- Shishido K., Ando T. Cleavage of ultraviolet light-irradiated DNA by single strand-specific S1 endonuclease. Biochem Biophys Res Commun. 1974 Aug 19;59(4):1380–1388. doi: 10.1016/0006-291x(74)90466-5. [DOI] [PubMed] [Google Scholar]
- Tullius T. D., Lippard S. J. Ethidium bromide changes the nuclease-sensitive DNA binding sites of the antitumor drug cis-diamminedichloroplatinum(II). Proc Natl Acad Sci U S A. 1982 Jun;79(11):3489–3492. doi: 10.1073/pnas.79.11.3489. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wani A. A., Hadi S. M. Partial purification and properties of an endonuclease from germinating pea seeds specific for single-stranded DNA. Arch Biochem Biophys. 1979 Aug;196(1):138–146. doi: 10.1016/0003-9861(79)90560-5. [DOI] [PubMed] [Google Scholar]
- Wiegand R. C., Godson G. N., Radding C. M. Specificity of the S1 nuclease from Aspergillus oryzae. J Biol Chem. 1975 Nov 25;250(22):8848–8855. [PubMed] [Google Scholar]
- Yamasaki H., Pulkrabek P., Grunberger D., Weinstein I. B. Differential excision from DNA of the C-8 and N2 guanosine adducts of N-acetyl-2-aminofluorene by single strand-specific endonucleases. Cancer Res. 1977 Oct;37(10):3756–3760. [PubMed] [Google Scholar]
- Yasuda S., Sekiguchi M. T4 endonuclease involved in repair of DNA. Proc Natl Acad Sci U S A. 1970 Dec;67(4):1839–1845. doi: 10.1073/pnas.67.4.1839. [DOI] [PMC free article] [PubMed] [Google Scholar]








