Effects of 3'-terminal phosphates in RNA produced by ribozyme cleavage.

نویسندگان

  • S L Alam
  • C C Nelson
  • B Felden
  • J F Atkins
  • R F Gesteland
چکیده

In vitro runoff transcription using T7 RNA polymerase has been the method of choice to produce milligram quantities of RNA for structural studies+ Unfortunately, the T7 enzyme often adds one or more extra nucleotides at the 39 end, which results in a heterogeneous RNA product (Milligan et al+, 1987)+ This heterogeneity can be observed at the 59 end as well, depending on the transcription template (Ferre-D’Amare & Doudna, 1996)+ The lack of homogeneity, which potentially is deleterious for structural studies, can be overcome with the use of cis-and/or trans-acting ribozymes,which produce clean RNA ends after their catalytic reaction (FerreD’Amare & Doudna, 1996)+ This procedure has been scaled up for large quantities of RNA for NMR and X-ray crystallographic studies, and is useful for purification of larger RNAs (greater than 50 nt) where singlenucleotide resolution by gel electrophoresis is difficult+ Ribozymes that have been used in this manner include the hairpin ribozyme, the hammerhead ribozyme (HH), the hepatitis delta ribozyme (d), and the Neurospora varkud satellite RNA ribozyme (VS) (Guo & Collins, 1995; Price et al+, 1995; Ferre-D’Amare & Doudna, 1996)+All of these ribozymes leave a 59-hydroxyl and a 39-cyclic phosphate as products of cleavage+ During the course of a structural investigation of a selenocysteine insertion element from rat Type 1 iodothyronine 59-deiodinase (D1 SECIS), we wished to prepare milligram quantities of an RNA that comprised the upper stem/loop of this RNA structure (41 nt; Fig+ 1A)+ This stem/loop is a stimulator required for the insertion of selenocysteins at a specific internal UGA stop codon (Berry et al+, 1991)+ Construction of the upper stem/ loop RNA required that the base of the stem end with four noncanonical base pairs (Walczak et al+, 1996), with no additional base pairing below this terminal quartet, as determined from in vitro assays (Martin et al+, 1998)+ This RNA has been produced synthetically for crystallization trials, so we sought a thorough comparison between this molecule and the RNA produced by run-off transcription+ Because the RNA to be studied begins with an adenosine and ends in a uridine, a ribozyme was used at each end to produce homogeneous RNA+ The system used to accomplish this has been described previously (Ferre-D’Amare & Doudna, 1996) and the resulting T7-produced RNA would differ from the synthetic RNA only by the 39cyclic phosphate+ In making preliminary imino proton NMR assignments for both of these RNAs, we concluded that the base pairing for both RNAs is nearly identical, as evident from the one-dimensional NMR spectra collected in 90% H2O (Fig+ 2)+ Close inspection shows that there are subtle differences near the RNA helix end (bracketed region)+ The terminal U-U iminos of the ribozymecleaved RNA stem/loop are not observed at 25 8C, or these imino protons have altered chemical shifts and become degenerate with other iminos of the G-U base pairs (assignments to be presented elsewhere)+ In addition, the two preceding G-A base pairs change in chemical shift and are broadened, as evident in spectra collected at several temperatures (25 8C and 5 8C; Fig+ 2 and insets)+ The resonance broadening results in a loss of NMR detection at temperatures above 35 8C+ At the same temperature, these signals are detected with the synthetic RNA+ These NMR spectral differences were not due to either 39or 59-heterogeneities as determined by electrospray mass spectrometry of each RNA (Fig+ 2)+ The observed spectral differences can be interpreted in at least two manners+ The broadening could arise from flattening of the ribose pucker (O49-endo or O49-exo) imposed by the cyclic phosphate at the 39 terminus (as seen with cyclic nucleoReprint requests to: Ray Gesteland, University of Utah, Department of Human Genetics, 15 N 2030 E, Rm 6160, Salt Lake City, Utah 84112-5330, USA; e-mail: rayg@genetics+med+utah+edu+ RNA (1998), 4:607–612+ Cambridge University Press+ Printed in the USA+ Copyright © 1998 RNA Society+

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عنوان ژورنال:
  • RNA

دوره 4 6  شماره 

صفحات  -

تاریخ انتشار 1998