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. 1987 Aug 25;15(16):6515–6538. doi: 10.1093/nar/15.16.6515

Localization of the in vivo and in vitro transcription initiation site and comparative analysis of the flanking sequences in the two main size classes of Ascaris lumbricoides rDNA.

G Briner, E Müller, H Neuhaus, E Back, F Müller, H Tobler
PMCID: PMC306120  PMID: 3502712

Abstract

An accurate in vitro transcription system which utilizes the cloned 8.8 and 8.4 kb size classes of Ascaris rRNA genes (pAlr8 and pAlr13) and two kinds of cellular extracts from Ascaris oogonia has been established. Both rDNA containing plasmids are efficiently transcribed in vitro by RNA polymerase I from a unique site of rDNA which corresponds to the in vivo initiation site. The in vitro transcription product has a triphosphorylated 5'-end and starts on a G localized 414 bp (pAlr8) upstream of the beginning of the mature 18S rRNA. The promoter region has been delimited by testing the in vitro template activity of a series of restriction fragments. The region essential for the accuracy of initiation is contained within nucleotides -72 to +65, but full efficiency of transcription requires the additional presence of the region from nucleotides +66 to +84. The sequences upstream from position -72 do not appear to modulate the efficiency of specific in vitro initiation. Furthermore, the sequences flanking the transcription initiation site from position -1500 to +570 have been determined in the two cloned representatives of the two rDNA main size classes.

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Selected References

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  1. Aeby P., Spicher A., de Chastonay Y., Müller F., Tobler H. Structure and genomic organization of proretrovirus-like elements partially eliminated from the somatic genome of Ascaris lumbricoides. EMBO J. 1986 Dec 1;5(12):3353–3360. doi: 10.1002/j.1460-2075.1986.tb04650.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Back E., Felder H., Müller F., Tobler H. Chromosomal arrangement of the two main rDNA size classes of Ascaris lumbricoides. Nucleic Acids Res. 1984 Feb 10;12(3):1333–1347. doi: 10.1093/nar/12.3.1333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Back E., Müller F., Tobler H. Structural organization of the two main rDNA size classes of Ascaris lumbricoides. Nucleic Acids Res. 1984 Feb 10;12(3):1313–1332. doi: 10.1093/nar/12.3.1313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Back E., Van Meir E., Müller F., Schaller D., Neuhaus H., Aeby P., Tobler H. Intervening sequences in the ribosomal RNA genes of Ascaris lumbricoides: DNA sequences at junctions and genomic organization. EMBO J. 1984 Nov;3(11):2523–2529. doi: 10.1002/j.1460-2075.1984.tb02167.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Berk A. J., Sharp P. A. Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids. Cell. 1977 Nov;12(3):721–732. doi: 10.1016/0092-8674(77)90272-0. [DOI] [PubMed] [Google Scholar]
  6. Cameron J. R., Loh E. Y., Davis R. W. Evidence for transposition of dispersed repetitive DNA families in yeast. Cell. 1979 Apr;16(4):739–751. doi: 10.1016/0092-8674(79)90090-4. [DOI] [PubMed] [Google Scholar]
  7. Clarkson S. G., Kurer V., Smith H. O. Sequence organization of a cloned tDNA met fragment from Xenopus laevis. Cell. 1978 Jul;14(3):713–724. doi: 10.1016/0092-8674(78)90253-2. [DOI] [PubMed] [Google Scholar]
  8. Foor W. E. Zygote formation in Ascaris lumbricoides (Nematoda). J Cell Biol. 1968 Oct;39(1):119–134. doi: 10.1083/jcb.39.1.119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Grummt I. Mapping of a mouse ribosomal DNA promoter by in vitro transcription. Nucleic Acids Res. 1981 Nov 25;9(22):6093–6102. doi: 10.1093/nar/9.22.6093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Grummt I. Nucleotide sequence requirements for specific initiation of transcription by RNA polymerase I. Proc Natl Acad Sci U S A. 1982 Nov;79(22):6908–6911. doi: 10.1073/pnas.79.22.6908. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Grummt I. Specific transcription of mouse ribosomal DNA in a cell-free system that mimics control in vivo. Proc Natl Acad Sci U S A. 1981 Feb;78(2):727–731. doi: 10.1073/pnas.78.2.727. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kaulenas M. S., Fairbairn D. RNA metabolism of fertilized Ascaris lumbricoides eggs during uterine development. Exp Cell Res. 1968 Sep;52(1):233–251. doi: 10.1016/0014-4827(68)90562-4. [DOI] [PubMed] [Google Scholar]
  13. Kaulenas M. S., Foor W. E., Fairbairn D. Ribosomal RNA synthesis during cleavage of Ascaris lumbricoides eggs. Science. 1969 Mar 14;163(3872):1201–1203. doi: 10.1126/science.163.3872.1201. [DOI] [PubMed] [Google Scholar]
  14. Kohorn B. D., Rae P. M. A component of Drosophila RNA polymerase I promoter lies within the rRNA transcription unit. Nature. 1983 Jul 14;304(5922):179–181. doi: 10.1038/304179a0. [DOI] [PubMed] [Google Scholar]
  15. Kohorn B. D., Rae P. M. Accurate transcription of truncated ribosomal DNA templates in a Drosophila cell-free system. Proc Natl Acad Sci U S A. 1982 Mar;79(5):1501–1505. doi: 10.1073/pnas.79.5.1501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kohorn B. D., Rae P. M. Localization of DNA sequences promoting RNA polymerase I activity in Drosophila. Proc Natl Acad Sci U S A. 1983 Jun;80(11):3265–3268. doi: 10.1073/pnas.80.11.3265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kownin P., Iida C. T., Brown-Shimer S., Paule M. R. The ribosomal RNA promoter of Acanthamoeba castellanii determined by transcription in a cell-free system. Nucleic Acids Res. 1985 Sep 11;13(17):6237–6248. doi: 10.1093/nar/13.17.6237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kuhn O., Tobler H. Quantitative analysis of RNA, glycogen and nucleotides from different developmental stages of Ascaris lumbricoides (var. suum). Biochim Biophys Acta. 1978 Nov 21;521(1):251–266. doi: 10.1016/0005-2787(78)90268-x. [DOI] [PubMed] [Google Scholar]
  19. Learned R. M., Smale S. T., Haltiner M. M., Tjian R. Regulation of human ribosomal RNA transcription. Proc Natl Acad Sci U S A. 1983 Jun;80(12):3558–3562. doi: 10.1073/pnas.80.12.3558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Learned R. M., Tjian R. In vitro transcription of human ribosomal RNA genes by RNA polymerase I. J Mol Appl Genet. 1982;1(6):575–584. [PubMed] [Google Scholar]
  21. Maniatis T., Efstratiadis A. Fractionation of low molecular weight DNA or RNA in polyacrylamide gels containing 98% formamide or 7 M urea. Methods Enzymol. 1980;65(1):299–305. doi: 10.1016/s0076-6879(80)65040-x. [DOI] [PubMed] [Google Scholar]
  22. Manley J. L., Fire A., Cano A., Sharp P. A., Gefter M. L. DNA-dependent transcription of adenovirus genes in a soluble whole-cell extract. Proc Natl Acad Sci U S A. 1980 Jul;77(7):3855–3859. doi: 10.1073/pnas.77.7.3855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. 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]
  24. McMaster G. K., Carmichael G. G. Analysis of single- and double-stranded nucleic acids on polyacrylamide and agarose gels by using glyoxal and acridine orange. Proc Natl Acad Sci U S A. 1977 Nov;74(11):4835–4838. doi: 10.1073/pnas.74.11.4835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. McStay B., Bird A. The origin of the rRNA precursor from Xenopus borealis, analysed in vivo and in vitro. Nucleic Acids Res. 1983 Dec 10;11(23):8167–8181. doi: 10.1093/nar/11.23.8167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Miesfeld R., Arnheim N. Identification of the in vivo and in vitro origin of transcription in human rDNA. Nucleic Acids Res. 1982 Jul 10;10(13):3933–3949. doi: 10.1093/nar/10.13.3933. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Miller K. G., Sollner-Webb B. Transcription of mouse rRNA genes by RNA polymerase I: in vitro and in vivo initiation and processing sites. Cell. 1981 Nov;27(1 Pt 2):165–174. doi: 10.1016/0092-8674(81)90370-6. [DOI] [PubMed] [Google Scholar]
  28. Miller K. G., Tower J., Sollner-Webb B. A complex control region of the mouse rRNA gene directs accurate initiation by RNA polymerase I. Mol Cell Biol. 1985 Mar;5(3):554–562. doi: 10.1128/mcb.5.3.554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Mishima Y., Yamamoto O., Kominami R., Muramatsu M. In vitro transcription of a cloned mouse ribosomal RNA gene. Nucleic Acids Res. 1981 Dec 21;9(24):6773–6785. doi: 10.1093/nar/9.24.6773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Noll F., Bielka H. Zur Biochemie der Embryogenese von Ascaris. I. Gehalt und Verteilungsmuster der Nukleins-auren. Acta Biol Med Ger. 1968;20(5):565–575. [PubMed] [Google Scholar]
  31. Paule M. R., Iida C. T., Perna P. J., Harris G. H., Brown Shimer S. L., Kownin P. Faithful initiation of ribosomal RNA transcription from cloned DNA by purified RNA polymerase I. Biochemistry. 1984 Aug 28;23(18):4167–4172. doi: 10.1021/bi00313a025. [DOI] [PubMed] [Google Scholar]
  32. Potter S. S., Brorein W. J., Jr, Dunsmuir P., Rubin G. M. Transposition of elements of the 412, copia and 297 dispersed repeated gene families in Drosophila. Cell. 1979 Jun;17(2):415–427. doi: 10.1016/0092-8674(79)90168-5. [DOI] [PubMed] [Google Scholar]
  33. Reeder R. H. Enhancers and ribosomal gene spacers. Cell. 1984 Sep;38(2):349–351. doi: 10.1016/0092-8674(84)90489-6. [DOI] [PubMed] [Google Scholar]
  34. Roop D. R., Nordstrom J. L., Tsai S. Y., Tsai M. J., O'Malley B. W. Transcription of structural and intervening sequences in the ovalbumin gene and identification of potential ovalbumin mRNA precursors. Cell. 1978 Oct;15(2):671–685. doi: 10.1016/0092-8674(78)90035-1. [DOI] [PubMed] [Google Scholar]
  35. 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]
  36. Skinner J. A., Ohrlein A., Grummt I. In vitro mutagenesis and transcriptional analysis of a mouse ribosomal promoter element. Proc Natl Acad Sci U S A. 1984 Apr;81(7):2137–2141. doi: 10.1073/pnas.81.7.2137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Sollner-Webb B., Reeder R. H. The nucleotide sequence of the initiation and termination sites for ribosomal RNA transcription in X. laevis. Cell. 1979 Oct;18(2):485–499. doi: 10.1016/0092-8674(79)90066-7. [DOI] [PubMed] [Google Scholar]
  38. Sollner-Webb B., Wilkinson J. A., Roan J., Reeder R. H. Nested control regions promote Xenopus ribosomal RNA synthesis by RNA polymerase I. Cell. 1983 Nov;35(1):199–206. doi: 10.1016/0092-8674(83)90222-2. [DOI] [PubMed] [Google Scholar]
  39. Sommerville J. RNA polymerase I promoters and transcription factors. Nature. 1984 Jul 19;310(5974):189–190. doi: 10.1038/310189a0. [DOI] [PubMed] [Google Scholar]
  40. Tomizawa J. I., Ohmori H., Bird R. E. Origin of replication of colicin E1 plasmid DNA. Proc Natl Acad Sci U S A. 1977 May;74(5):1865–1869. doi: 10.1073/pnas.74.5.1865. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Wahli W., Germond J. E., ten Heggeler B., May F. E. Vitellogenin genes A1 and B1 are linked in the Xenopus laevis genome. Proc Natl Acad Sci U S A. 1982 Nov;79(22):6832–6836. doi: 10.1073/pnas.79.22.6832. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Weil P. A., Luse D. S., Segall J., Roeder R. G. Selective and accurate initiation of transcription at the Ad2 major late promotor in a soluble system dependent on purified RNA polymerase II and DNA. Cell. 1979 Oct;18(2):469–484. doi: 10.1016/0092-8674(79)90065-5. [DOI] [PubMed] [Google Scholar]
  43. Whitaker J. R., Granum P. E. An absolute method for protein determination based on difference in absorbance at 235 and 280 nm. Anal Biochem. 1980 Nov 15;109(1):156–159. doi: 10.1016/0003-2697(80)90024-x. [DOI] [PubMed] [Google Scholar]
  44. Wilkinson J. K., Sollner-Webb B. Transcription of Xenopus ribosomal RNA genes by RNA polymerase I in vitro. J Biol Chem. 1982 Dec 10;257(23):14375–14383. [PubMed] [Google Scholar]
  45. Yamamoto O., Takakusa N., Mishima Y., Kominami R., Muramatsu M. Determination of the promoter region of mouse ribosomal RNA gene by an in vitro transcription system. Proc Natl Acad Sci U S A. 1984 Jan;81(2):299–303. doi: 10.1073/pnas.81.2.299. [DOI] [PMC free article] [PubMed] [Google Scholar]

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