Abstract
Immature oocytes from Xenopus laevis contain a 42S ribonucleoprotein particle (RNP) containing 5S RNA, tRNA, a 43 kDa protein, and a 48 kDa protein. A particle containing 5S RNA and the 43 kDa protein (p43-5S) liberated from the 42S particle upon brief treatment with urea can be purified by anion exchange chromatography. The purified p43-5S RNA migrates as a distinct species during electrophoresis on native polyacrylamide gels. Radiolabeled 5S RNA can be incorporated into the p43-5S complex by an RNA exchange reaction. The resulting complexes containing labeled 5S RNA have a mobility on polyacrylamide gels identical to that of purified p43-5S RNPs. RNP complexes containing 5S RNA labeled at either the 5' or 3' end were probed with a variety of nucleases in order to identify residues protected by p43. Nuclease protection assays performed with alpha-sarcin indicate that p43 binds primarily helices I, II, IV, and V of 5S RNA. This is the same general binding site observed for TFIIIA on 5S RNA. Direct comparison of the binding sites of p43 and TFIIIA with T1 and cobra venom nucleases reveals striking differences in the protection patterns of these two proteins.
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.
- Andersen J., Delihas N. Characterization of RNA-protein interactions in 7 S ribonucleoprotein particles from Xenopus laevis oocytes. J Biol Chem. 1986 Feb 25;261(6):2912–2917. [PubMed] [Google Scholar]
- Andersen J., Delihas N., Hanas J. S., Wu C. W. 5S RNA structure and interaction with transcription factor A. 2. Ribonuclease probe of the 7S particle from Xenopus laevis immature oocytes and RNA exchange properties of the 7S particle. Biochemistry. 1984 Nov 20;23(24):5759–5766. doi: 10.1021/bi00319a014. [DOI] [PubMed] [Google Scholar]
- Aoyama K., Tanaka T., Hidaka S., Ishikawa K. Binding sites of rat liver 5S RNA to ribosomal protein L5. J Biochem. 1984 Apr;95(4):1179–1186. doi: 10.1093/oxfordjournals.jbchem.a134707. [DOI] [PubMed] [Google Scholar]
- Barrett P., Sommerville J. An alternative protein factor which binds the internal promoter of Xenopus 5S ribosomal RNA genes. Nucleic Acids Res. 1987 Nov 11;15(21):8679–8691. doi: 10.1093/nar/15.21.8679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Christiansen J., Brown R. S., Sproat B. S., Garrett R. A. Xenopus transcription factor IIIA binds primarily at junctions between double helical stems and internal loops in oocyte 5S RNA. EMBO J. 1987 Feb;6(2):453–460. doi: 10.1002/j.1460-2075.1987.tb04775.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Denis H., le Maire M. Thesaurisomes, a novel kind of nucleoprotein particle. Subcell Biochem. 1983;9:263–297. doi: 10.1007/978-1-4613-3533-7_3. [DOI] [PubMed] [Google Scholar]
- Donis-Keller H., Maxam A. M., Gilbert W. Mapping adenines, guanines, and pyrimidines in RNA. Nucleic Acids Res. 1977 Aug;4(8):2527–2538. doi: 10.1093/nar/4.8.2527. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dumont J. N. Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals. J Morphol. 1972 Feb;136(2):153–179. doi: 10.1002/jmor.1051360203. [DOI] [PubMed] [Google Scholar]
- Endo Y., Huber P. W., Wool I. G. The ribonuclease activity of the cytotoxin alpha-sarcin. The characteristics of the enzymatic activity of alpha-sarcin with ribosomes and ribonucleic acids as substrates. J Biol Chem. 1983 Feb 25;258(4):2662–2667. [PubMed] [Google Scholar]
- Engelke D. R., Ng S. Y., Shastry B. S., Roeder R. G. Specific interaction of a purified transcription factor with an internal control region of 5S RNA genes. Cell. 1980 Mar;19(3):717–728. doi: 10.1016/s0092-8674(80)80048-1. [DOI] [PubMed] [Google Scholar]
- Ford P. J. Non-coordinated accumulation and synthesis of 5S ribonucleic acid by ovaries of Xenopus laevis. Nature. 1971 Oct 22;233(5321):561–564. doi: 10.1038/233561a0. [DOI] [PubMed] [Google Scholar]
- Hanas J. S., Bogenhagen D. F., Wu C. W. Cooperative model for the binding of Xenopus transcription factor A to the 5S RNA gene. Proc Natl Acad Sci U S A. 1983 Apr;80(8):2142–2145. doi: 10.1073/pnas.80.8.2142. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Honda B. M., Roeder R. G. Association of a 5S gene transcription factor with 5S RNA and altered levels of the factor during cell differentiation. Cell. 1980 Nov;22(1 Pt 1):119–126. doi: 10.1016/0092-8674(80)90160-9. [DOI] [PubMed] [Google Scholar]
- Huber P. W., Wool I. G. Identification of the binding site on 5S rRNA for the transcription factor IIIA: proposed structure of a common binding site on 5S rRNA and on the gene. Proc Natl Acad Sci U S A. 1986 Mar;83(6):1593–1597. doi: 10.1073/pnas.83.6.1593. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huber P. W., Wool I. G. Nuclease protection analysis of ribonucleoprotein complexes: use of the cytotoxic ribonuclease alpha-sarcin to determine the binding sites for Escherichia coli ribosomal proteins L5, L18, and L25 on 5S rRNA. Proc Natl Acad Sci U S A. 1984 Jan;81(2):322–326. doi: 10.1073/pnas.81.2.322. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huber P. W., Wool I. G. Use of the cytotoxic nuclease alpha-sarcin to identify the binding site on eukaryotic 5 S ribosomal ribonucleic acid for the ribosomal protein L5. J Biol Chem. 1986 Mar 5;261(7):3002–3005. [PubMed] [Google Scholar]
- Joho K. E., Darby M. K., Crawford E. T., Brown D. D. A finger protein structurally similar to TFIIIA that binds exclusively to 5S RNA in Xenopus. Cell. 1990 Apr 20;61(2):293–300. doi: 10.1016/0092-8674(90)90809-s. [DOI] [PubMed] [Google Scholar]
- Kloetzel P. M., Whitfield W., Sommerville J. Analysis of reconstruction of an RNP particle which stores 5S RNA and tRNA in amphibian oocytes. Nucleic Acids Res. 1981 Feb 11;9(3):605–621. doi: 10.1093/nar/9.3.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lockard R. E., Kumar A. Mapping tRNA structure in solution using double-strand-specific ribonuclease V1 from cobra venom. Nucleic Acids Res. 1981 Oct 10;9(19):5125–5140. doi: 10.1093/nar/9.19.5125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mattaj I. W., Coppard N. J., Brown R. S., Clark B. F., De Robertis E. M. 42S p48--the most abundant protein in previtellogenic Xenopus oocytes--resembles elongation factor 1 alpha structurally and functionally. EMBO J. 1987 Aug;6(8):2409–2413. doi: 10.1002/j.1460-2075.1987.tb02519.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller J., McLachlan A. D., Klug A. Repetitive zinc-binding domains in the protein transcription factor IIIA from Xenopus oocytes. EMBO J. 1985 Jun;4(6):1609–1614. doi: 10.1002/j.1460-2075.1985.tb03825.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pelham H. R., Brown D. D. A specific transcription factor that can bind either the 5S RNA gene or 5S RNA. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4170–4174. doi: 10.1073/pnas.77.7.4170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Picard B., Wegnez M. Isolation of a 7S particle from Xenopus laevis oocytes: a 5S RNA-protein complex. Proc Natl Acad Sci U S A. 1979 Jan;76(1):241–245. doi: 10.1073/pnas.76.1.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Picard B., le Maire M., Wegnez M., Denis H. Biochemical Research on oogenesis. Composition of the 42-S storage particles of Xenopus laevix oocytes. Eur J Biochem. 1980 Aug;109(2):359–368. doi: 10.1111/j.1432-1033.1980.tb04802.x. [DOI] [PubMed] [Google Scholar]
- Pieler T., Guddat U., Oei S. L., Erdmann V. A. Analysis of the RNA structural elements involved in the binding of the transcription factor III A from Xenopus laevis. Nucleic Acids Res. 1986 Aug 11;14(15):6313–6326. doi: 10.1093/nar/14.15.6313. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Romaniuk P. J. Characterization of the RNA binding properties of transcription factor IIIA of Xenopus laevis oocytes. Nucleic Acids Res. 1985 Jul 25;13(14):5369–5387. doi: 10.1093/nar/13.14.5369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Romaniuk P. J., de Stevenson I. L., Wong H. H. Defining the binding site of Xenopus transcription factor IIIA on 5S RNA using truncated and chimeric 5S RNA molecules. Nucleic Acids Res. 1987 Mar 25;15(6):2737–2755. doi: 10.1093/nar/15.6.2737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sands M. S., Bogenhagen D. F. TFIIIA binds to different domains of 5S RNA and the Xenopus borealis 5S RNA gene. Mol Cell Biol. 1987 Nov;7(11):3985–3993. doi: 10.1128/mcb.7.11.3985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith D. R., Jackson I. J., Brown D. D. Domains of the positive transcription factor specific for the Xenopus 5S RNA gene. Cell. 1984 Jun;37(2):645–652. doi: 10.1016/0092-8674(84)90396-9. [DOI] [PubMed] [Google Scholar]
- Vasilenko S. K., Ryte V. C. [Isolation of highly purified ribonuclease from cobra (Naja oxiana) venom]. Biokhimiia. 1975 May-Jun;40(3):578–583. [PubMed] [Google Scholar]
- Wakefield L., Gurdon J. B. Cytoplasmic regulation of 5S RNA genes in nuclear-transplant embryos. EMBO J. 1983;2(9):1613–1619. doi: 10.1002/j.1460-2075.1983.tb01632.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Westhof E., Romby P., Romaniuk P. J., Ebel J. P., Ehresmann C., Ehresmann B. Computer modeling from solution data of spinach chloroplast and of Xenopus laevis somatic and oocyte 5 S rRNAs. J Mol Biol. 1989 May 20;207(2):417–431. doi: 10.1016/0022-2836(89)90264-7. [DOI] [PubMed] [Google Scholar]





