Abstract
A current model for transcription-coupled DNA repair is that RNA polymerase, arrested at a DNA lesion, directs the repair machinery to the transcribed strand of an active gene. To help elucidate this role of RNA polymerase, we constructed DNA templates containing the major late promoter of adenovirus and a cyclobutane pyrimidine dimer (CPD) at a specific site. CPDs, the predominant DNA lesions formed by ultraviolet radiation, are good substrates for transcription-coupled repair. A CPD located on the transcribed strand of the template was a strong block to polymerase movement, whereas a CPD located on the nontranscribed strand had no effect on transcription. Furthermore, the arrested polymerase shielded the CPD from recognition by photolyase, a bacterial DNA repair protein. Transcription elongation factor SII (also called TFIIS) facilitates read-through of a variety of transcriptional pause sites by a process in which RNA polymerase II cleaves the nascent transcript before elongation resumes. We show that SII induces nascent transcript cleavage by RNA polymerase II stalled at a CPD. However, this cleavage does not remove the arrested polymerase from the site of the DNA lesion, nor does it facilitate translesional bypass by the polymerase. The arrested ternary complex is stable and competent to resume elongation, demonstrating that neither the polymerase nor the RNA product dissociates from the DNA template.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bohr V. A., Smith C. A., Okumoto D. S., Hanawalt P. C. DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall. Cell. 1985 Feb;40(2):359–369. doi: 10.1016/0092-8674(85)90150-3. [DOI] [PubMed] [Google Scholar]
- Borukhov S., Sagitov V., Goldfarb A. Transcript cleavage factors from E. coli. Cell. 1993 Feb 12;72(3):459–466. doi: 10.1016/0092-8674(93)90121-6. [DOI] [PubMed] [Google Scholar]
- Carreau M., Hunting D. Transcription-dependent and independent DNA excision repair pathways in human cells. Mutat Res. 1992 Jun;274(1):57–64. doi: 10.1016/0921-8777(92)90043-3. [DOI] [PubMed] [Google Scholar]
- Chamberlin M. J. New models for the mechanism of transcription elongation and its regulation. Harvey Lect. 1992 1993;88:1–21. [PubMed] [Google Scholar]
- Christians F. C., Hanawalt P. C. Inhibition of transcription and strand-specific DNA repair by alpha-amanitin in Chinese hamster ovary cells. Mutat Res. 1992 Aug;274(2):93–101. doi: 10.1016/0921-8777(92)90056-9. [DOI] [PubMed] [Google Scholar]
- Christians F. C., Hanawalt P. C. Lack of transcription-coupled repair in mammalian ribosomal RNA genes. Biochemistry. 1993 Oct 5;32(39):10512–10518. doi: 10.1021/bi00090a030. [DOI] [PubMed] [Google Scholar]
- Christie K. R., Awrey D. E., Edwards A. M., Kane C. M. Purified yeast RNA polymerase II reads through intrinsic blocks to elongation in response to the yeast TFIIS analogue, P37. J Biol Chem. 1994 Jan 14;269(2):936–943. [PubMed] [Google Scholar]
- Eilat D., Hochberg M., Fischel R., Laskov R. Antibodies to RNA from autoimmune NZB/NZW mice recognize a similar antigenic determinant and show a large idiotypic diversity. Proc Natl Acad Sci U S A. 1982 Jun;79(12):3818–3822. doi: 10.1073/pnas.79.12.3818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Green C. L., Loechler E. L., Fowler K. W., Essigmann J. M. Construction and characterization of extrachromosomal probes for mutagenesis by carcinogens: site-specific incorporation of O6-methylguanine into viral and plasmid genomes. Proc Natl Acad Sci U S A. 1984 Jan;81(1):13–17. doi: 10.1073/pnas.81.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gu W., Powell W., Mote J., Jr, Reines D. Nascent RNA cleavage by arrested RNA polymerase II does not require upstream translocation of the elongation complex on DNA. J Biol Chem. 1993 Dec 5;268(34):25604–25616. [PMC free article] [PubMed] [Google Scholar]
- Guo H., Price D. H. Mechanism of DmS-II-mediated pause suppression by Drosophila RNA polymerase II. J Biol Chem. 1993 Sep 5;268(25):18762–18770. [PubMed] [Google Scholar]
- Hanawalt P., Mellon I. Stranded in an active gene. Curr Biol. 1993 Jan;3(1):67–69. doi: 10.1016/0960-9822(93)90156-i. [DOI] [PubMed] [Google Scholar]
- Horikoshi M., Sekimizu K., Natori S. Analysis of the stimulatory factor of RNA polymerase II in the initiation and elongation complex. J Biol Chem. 1984 Jan 10;259(1):608–611. [PubMed] [Google Scholar]
- Huang J. C., Svoboda D. L., Reardon J. T., Sancar A. Human nucleotide excision nuclease removes thymine dimers from DNA by incising the 22nd phosphodiester bond 5' and the 6th phosphodiester bond 3' to the photodimer. Proc Natl Acad Sci U S A. 1992 Apr 15;89(8):3664–3668. doi: 10.1073/pnas.89.8.3664. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Izban M. G., Luse D. S. The RNA polymerase II ternary complex cleaves the nascent transcript in a 3'----5' direction in the presence of elongation factor SII. Genes Dev. 1992 Jul;6(7):1342–1356. doi: 10.1101/gad.6.7.1342. [DOI] [PubMed] [Google Scholar]
- Izban M. G., Luse D. S. The increment of SII-facilitated transcript cleavage varies dramatically between elongation competent and incompetent RNA polymerase II ternary complexes. J Biol Chem. 1993 Jun 15;268(17):12874–12885. [PubMed] [Google Scholar]
- Kerppola T. K., Kane C. M. Analysis of the signals for transcription termination by purified RNA polymerase II. Biochemistry. 1990 Jan 9;29(1):269–278. doi: 10.1021/bi00453a037. [DOI] [PubMed] [Google Scholar]
- Leadon S. A., Lawrence D. A. Preferential repair of DNA damage on the transcribed strand of the human metallothionein genes requires RNA polymerase II. Mutat Res. 1991 Jul;255(1):67–78. doi: 10.1016/0921-8777(91)90019-l. [DOI] [PubMed] [Google Scholar]
- Leadon S. A., Lawrence D. A. Strand-selective repair of DNA damage in the yeast GAL7 gene requires RNA polymerase II. J Biol Chem. 1992 Nov 15;267(32):23175–23182. [PubMed] [Google Scholar]
- Mellon I., Bohr V. A., Smith C. A., Hanawalt P. C. Preferential DNA repair of an active gene in human cells. Proc Natl Acad Sci U S A. 1986 Dec;83(23):8878–8882. doi: 10.1073/pnas.83.23.8878. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mellon I., Hanawalt P. C. Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand. Nature. 1989 Nov 2;342(6245):95–98. doi: 10.1038/342095a0. [DOI] [PubMed] [Google Scholar]
- Mellon I., Spivak G., Hanawalt P. C. Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene. Cell. 1987 Oct 23;51(2):241–249. doi: 10.1016/0092-8674(87)90151-6. [DOI] [PubMed] [Google Scholar]
- Mote J., Jr, Ghanouni P., Reines D. A DNA minor groove-binding ligand both potentiates and arrests transcription by RNA polymerase II. Elongation factor SII enables readthrough at arrest sites. J Mol Biol. 1994 Feb 25;236(3):725–737. doi: 10.1006/jmbi.1994.1185. [DOI] [PubMed] [Google Scholar]
- Qian X., Gozani S. N., Yoon H., Jeon C. J., Agarwal K., Weiss M. A. Novel zinc finger motif in the basal transcriptional machinery: three-dimensional NMR studies of the nucleic acid binding domain of transcriptional elongation factor TFIIS. Biochemistry. 1993 Sep 28;32(38):9944–9959. doi: 10.1021/bi00089a010. [DOI] [PubMed] [Google Scholar]
- Reinberg D., Roeder R. G. Factors involved in specific transcription by mammalian RNA polymerase II. Transcription factor IIS stimulates elongation of RNA chains. J Biol Chem. 1987 Mar 5;262(7):3331–3337. [PubMed] [Google Scholar]
- Reines D., Mote J., Jr Elongation factor SII-dependent transcription by RNA polymerase II through a sequence-specific DNA-binding protein. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1917–1921. doi: 10.1073/pnas.90.5.1917. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reines D. RNA polymerase II elongation complex. Elongation complexes purified using an anti-RNA antibody do not contain initiation factor alpha. J Biol Chem. 1991 Jun 5;266(16):10510–10517. [PMC free article] [PubMed] [Google Scholar]
- Sauerbier W., Hercules K. Gene and transcription unit mapping by radiation effects. Annu Rev Genet. 1978;12:329–363. doi: 10.1146/annurev.ge.12.120178.001553. [DOI] [PubMed] [Google Scholar]
- Sawadogo M., Sentenac A., Fromageot P. Interaction of a new polypeptide with yeast RNA polymerase B. J Biol Chem. 1980 Jan 10;255(1):12–15. [PubMed] [Google Scholar]
- Selby C. P., Sancar A. Molecular mechanism of transcription-repair coupling. Science. 1993 Apr 2;260(5104):53–58. doi: 10.1126/science.8465200. [DOI] [PubMed] [Google Scholar]
- Selby C. P., Sancar A. Transcription preferentially inhibits nucleotide excision repair of the template DNA strand in vitro. J Biol Chem. 1990 Dec 5;265(34):21330–21336. [PubMed] [Google Scholar]
- Sluder A. E., Greenleaf A. L., Price D. H. Properties of a Drosophila RNA polymerase II elongation factor. J Biol Chem. 1989 May 25;264(15):8963–8969. [PubMed] [Google Scholar]
- Smerdon M. J., Thoma F. Site-specific DNA repair at the nucleosome level in a yeast minichromosome. Cell. 1990 May 18;61(4):675–684. doi: 10.1016/0092-8674(90)90479-x. [DOI] [PubMed] [Google Scholar]
- Sweder K. S., Hanawalt P. C. Preferential repair of cyclobutane pyrimidine dimers in the transcribed strand of a gene in yeast chromosomes and plasmids is dependent on transcription. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10696–10700. doi: 10.1073/pnas.89.22.10696. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsuboi A., Conger K., Garrett K. P., Conaway R. C., Conaway J. W., Arai N. RNA polymerase II initiation factor alpha from rat liver is almost identical to human TFIIB. Nucleic Acids Res. 1992 Jun 25;20(12):3250–3250. doi: 10.1093/nar/20.12.3250. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van Houten B. Nucleotide excision repair in Escherichia coli. Microbiol Rev. 1990 Mar;54(1):18–51. doi: 10.1128/mr.54.1.18-51.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vos J. M., Wauthier E. L. Differential introduction of DNA damage and repair in mammalian genes transcribed by RNA polymerases I and II. Mol Cell Biol. 1991 Apr;11(4):2245–2252. doi: 10.1128/mcb.11.4.2245. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang D., Hawley D. K. Identification of a 3'-->5' exonuclease activity associated with human RNA polymerase II. Proc Natl Acad Sci U S A. 1993 Feb 1;90(3):843–847. doi: 10.1073/pnas.90.3.843. [DOI] [PMC free article] [PubMed] [Google Scholar]