Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1992 Dec 11;20(23):6347–6353. doi: 10.1093/nar/20.23.6347

The protein sequence and some intron positions are conserved between the switching gene swi10 of Schizosaccharomyces pombe and the human excision repair gene ERCC1.

C Rödel 1, S Kirchhoff 1, H Schmidt 1
PMCID: PMC334526  PMID: 1475195

Abstract

The switching gene swi10+ has a function in mating-type switching as well as in the repair of radiation damages. We have cloned the genomic swi10+ gene by functional complementation of the switching defect of the swi10-154 mutant. The swi10+ gene is not essential for viability. The DNA sequence revealed an open reading frame of 759 nucleotides interrupted by three introns of 127, 52 and 60 bp, respectively. The positions of intron I as well as of intron III of swi10 are evolutionary conserved in comparison to the introns III and IV of the human ERCC1 gene. The analysis of cDNA clones isolated by PCR amplification confirmed the structure of the swi10 gene. The putative Swi10 protein has homologies to the human and mouse ERCC1 protein, to Rad10 of Saccharomyces cerevisiae and to parts of UvrA and UvrC of E. coli. All these proteins are essential components for excision repair of damaged DNA. The Swi10 protein contains a putative DNA binding domain previously found in other proteins. Northern blot experiments and the analyses of cDNA clones indicate that intron I of the swi10 gene is not efficiently spliced.

Full text

PDF
6347

Images in this article

Selected References

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

  1. Bach M. L. Cloning and expression of the OMP decarboxylase gene URA4 from Schizosaccharomyces pombe. Curr Genet. 1987;12(7):527–534. doi: 10.1007/BF00419562. [DOI] [PubMed] [Google Scholar]
  2. Bröker M., Bäuml O. New expression vectors for the fission yeast Schizosaccharomyces pombe. FEBS Lett. 1989 May 8;248(1-2):105–110. doi: 10.1016/0014-5793(89)80441-7. [DOI] [PubMed] [Google Scholar]
  3. Desplan C., Theis J., O'Farrell P. H. The Drosophila developmental gene, engrailed, encodes a sequence-specific DNA binding activity. Nature. 1985 Dec 19;318(6047):630–635. doi: 10.1038/318630a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Egel R., Beach D. H., Klar A. J. Genes required for initiation and resolution steps of mating-type switching in fission yeast. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3481–3485. doi: 10.1073/pnas.81.11.3481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Engebrecht J. A., Voelkel-Meiman K., Roeder G. S. Meiosis-specific RNA splicing in yeast. Cell. 1991 Sep 20;66(6):1257–1268. doi: 10.1016/0092-8674(91)90047-3. [DOI] [PubMed] [Google Scholar]
  6. Fabre F. Relation between repair mechanisms and induced mitotic recombination after UV irradiation, in the yeast Schizosaccharomyces pombe. Effects of caffeine. Mol Gen Genet. 1972;117(2):153–166. doi: 10.1007/BF00267612. [DOI] [PubMed] [Google Scholar]
  7. Fikes J. D., Becker D. M., Winston F., Guarente L. Striking conservation of TFIID in Schizosaccharomyces pombe and Saccharomyces cerevisiae. Nature. 1990 Jul 19;346(6281):291–294. doi: 10.1038/346291a0. [DOI] [PubMed] [Google Scholar]
  8. Fleck O., Heim L., Gutz H. A mutated swi4 gene causes duplications in the mating-type region of Schizosaccharomyces pombe. Curr Genet. 1990 Dec;18(6):501–509. doi: 10.1007/BF00327020. [DOI] [PubMed] [Google Scholar]
  9. Fleck O., Michael H., Heim L. The swi4+ gene of Schizosaccharomyces pombe encodes a homologue of mismatch repair enzymes. Nucleic Acids Res. 1992 May 11;20(9):2271–2278. doi: 10.1093/nar/20.9.2271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gilbert W. Genes-in-pieces revisited. Science. 1985 May 17;228(4701):823–824. doi: 10.1126/science.4001923. [DOI] [PubMed] [Google Scholar]
  11. Gill D. R., Hatfull G. F., Salmond G. P. A new cell division operon in Escherichia coli. Mol Gen Genet. 1986 Oct;205(1):134–145. doi: 10.1007/BF02428043. [DOI] [PubMed] [Google Scholar]
  12. Henikoff S. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene. 1984 Jun;28(3):351–359. doi: 10.1016/0378-1119(84)90153-7. [DOI] [PubMed] [Google Scholar]
  13. Hoeijmakers J. H., van Duin M., Westerveld A., Yasui A., Bootsma D. Identification of DNA repair genes in the human genome. Cold Spring Harb Symp Quant Biol. 1986;51(Pt 1):91–101. doi: 10.1101/sqb.1986.051.01.012. [DOI] [PubMed] [Google Scholar]
  14. Husain I., Van Houten B., Thomas D. C., Sancar A. Sequences of Escherichia coli uvrA gene and protein reveal two potential ATP binding sites. J Biol Chem. 1986 Apr 15;261(11):4895–4901. [PubMed] [Google Scholar]
  15. Ito H., Fukuda Y., Murata K., Kimura A. Transformation of intact yeast cells treated with alkali cations. J Bacteriol. 1983 Jan;153(1):163–168. doi: 10.1128/jb.153.1.163-168.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Johnson A. D., Herskowitz I. A repressor (MAT alpha 2 Product) and its operator control expression of a set of cell type specific genes in yeast. Cell. 1985 Aug;42(1):237–247. doi: 10.1016/s0092-8674(85)80119-7. [DOI] [PubMed] [Google Scholar]
  17. Jones R. H., Moreno S., Nurse P., Jones N. C. Expression of the SV40 promoter in fission yeast: identification and characterization of an AP-1-like factor. Cell. 1988 May 20;53(4):659–667. doi: 10.1016/0092-8674(88)90581-8. [DOI] [PubMed] [Google Scholar]
  18. LEUPOLD U. Methodisches zur Genetik von Schizosaccharomyces pombe. Schweiz Z Pathol Bakteriol. 1955;18(5):1141–1146. [PubMed] [Google Scholar]
  19. Laughon A., Scott M. P. Sequence of a Drosophila segmentation gene: protein structure homology with DNA-binding proteins. Nature. 1984 Jul 5;310(5972):25–31. doi: 10.1038/310025a0. [DOI] [PubMed] [Google Scholar]
  20. Losson R., Lacroute F. Plasmids carrying the yeast OMP decarboxylase structural and regulatory genes: transcription regulation in a foreign environment. Cell. 1983 Feb;32(2):371–377. doi: 10.1016/0092-8674(83)90456-7. [DOI] [PubMed] [Google Scholar]
  21. Messing J. New M13 vectors for cloning. Methods Enzymol. 1983;101:20–78. doi: 10.1016/0076-6879(83)01005-8. [DOI] [PubMed] [Google Scholar]
  22. Nischt R., Thüroff E., Küfer N. F. Molecular cloning of a ribosomal protein gene from the fission yeast Schizosaccharomyces pombe. Curr Genet. 1986;10(5):365–370. doi: 10.1007/BF00418408. [DOI] [PubMed] [Google Scholar]
  23. Pearson W. R., Lipman D. J. Improved tools for biological sequence comparison. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2444–2448. doi: 10.1073/pnas.85.8.2444. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Porter S. D., Smith M. Homoeo-domain homology in yeast MAT alpha 2 is essential for repressor activity. Nature. 1986 Apr 24;320(6064):766–768. doi: 10.1038/320766a0. [DOI] [PubMed] [Google Scholar]
  25. Prabhala G., Rosenberg G. H., Käufer N. F. Architectural features of pre-mRNA introns in the fission yeast Schizosaccharomyces pombe. Yeast. 1992 Mar;8(3):171–182. doi: 10.1002/yea.320080303. [DOI] [PubMed] [Google Scholar]
  26. Reynolds P., Prakash L., Dumais D., Perozzi G., Prakash S. Nucleotide sequence of the RAD10 gene of Saccharomyces cerevisiae. EMBO J. 1985 Dec 16;4(13A):3549–3552. doi: 10.1002/j.1460-2075.1985.tb04115.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Rothstein R. J. One-step gene disruption in yeast. Methods Enzymol. 1983;101:202–211. doi: 10.1016/0076-6879(83)01015-0. [DOI] [PubMed] [Google Scholar]
  28. Russell P., Nurse P. Schizosaccharomyces pombe and Saccharomyces cerevisiae: a look at yeasts divided. Cell. 1986 Jun 20;45(6):781–782. doi: 10.1016/0092-8674(86)90550-7. [DOI] [PubMed] [Google Scholar]
  29. Sancar A., Sancar G. B. DNA repair enzymes. Annu Rev Biochem. 1988;57:29–67. doi: 10.1146/annurev.bi.57.070188.000333. [DOI] [PubMed] [Google Scholar]
  30. Sancar G. B., Sancar A., Rupp W. D. Sequences of the E. coli uvrC gene and protein. Nucleic Acids Res. 1984 Jun 11;12(11):4593–4608. doi: 10.1093/nar/12.11.4593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. 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]
  32. Schmidt H., Kapitza-Fecke P., Stephen E. R., Gutz H. Some of the swi genes of Schizosaccharomyces pombe also have a function in the repair of radiation damage. Curr Genet. 1989 Aug;16(2):89–94. doi: 10.1007/BF00393400. [DOI] [PubMed] [Google Scholar]
  33. Sung P., Prakash L., Prakash S. Renaturation of DNA catalysed by yeast DNA repair and recombination protein RAD10. Nature. 1992 Feb 20;355(6362):743–745. doi: 10.1038/355743a0. [DOI] [PubMed] [Google Scholar]
  34. Vieira J., Messing J. The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene. 1982 Oct;19(3):259–268. doi: 10.1016/0378-1119(82)90015-4. [DOI] [PubMed] [Google Scholar]
  35. Wright A. P., Maundrell K., Shall S. Transformation of Schizosaccharomyces pombe by non-homologous, unstable integration of plasmids in the genome. Curr Genet. 1986;10(7):503–508. doi: 10.1007/BF00447383. [DOI] [PubMed] [Google Scholar]
  36. Wright A., Maundrell K., Heyer W. D., Beach D., Nurse P. Vectors for the construction of gene banks and the integration of cloned genes in Schizosaccharomyces pombe and Saccharomyces cerevisiae. Plasmid. 1986 Mar;15(2):156–158. doi: 10.1016/0147-619x(86)90051-x. [DOI] [PubMed] [Google Scholar]
  37. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  38. van Duin M., Koken M. H., van den Tol J., ten Dijke P., Odijk H., Westerveld A., Bootsma D., Hoeijmakers J. H. Genomic characterization of the human DNA excision repair gene ERCC-1. Nucleic Acids Res. 1987 Nov 25;15(22):9195–9213. doi: 10.1093/nar/15.22.9195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. van Duin M., de Wit J., Odijk H., Westerveld A., Yasui A., Koken M. H., Hoeijmakers J. H., Bootsma D. Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. Cell. 1986 Mar 28;44(6):913–923. doi: 10.1016/0092-8674(86)90014-0. [DOI] [PubMed] [Google Scholar]
  40. van Duin M., van den Tol J., Warmerdam P., Odijk H., Meijer D., Westerveld A., Bootsma D., Hoeijmakers J. H. Evolution and mutagenesis of the mammalian excision repair gene ERCC-1. Nucleic Acids Res. 1988 Jun 24;16(12):5305–5322. doi: 10.1093/nar/16.12.5305. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES