Evidence map›Paper›PMID 18227152›Full record

ArticleMolecular and cellular biology2008

Trypanosoma brucei RNA editing: coupled cycles of U deletion reveal processive activity of the editing complex.

Vadim S Alatortsev, Jorge Cruz-Reyes, Alevtina G Zhelonkina, Barbara Sollner-Webb

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

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  11. When you can't trust the DNA: RNA editing changes transcript sequences.Cellular and molecular life sciences : CMLS · 2011
    Review
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Vadim S AlatortsevDepartment of Biological Chemistry, Johns Hopkins University School of Medicine, 725 N. Wolfe Street, Baltimore, MD 21205, USA.
Jorge Cruz-Reyes
Alevtina G Zhelonkina
Barbara Sollner-Webb

Funding

SPECIFICITY OF RNA MATURATIONR01GM034231 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SOLLNER-WEBB, BARBARA · 1985 to 2005
$2.1M
NIGMS NIH HHS GM 34231NIGMS NIH HHS R01 GM034231
6 · The paper itself

Abstract

RNA editing in Trypanosoma brucei is posttranscriptional uridylate removal/addition, generally at vast numbers of pre-mRNA sites, but to date, only single editing cycles have been examined in vitro. We here demonstrate achieving sequential cycles of U deletion in vitro, with editing products confirmed by sequence analysis. Notably, the subsequent editing cycle is much more efficient and occurs far more rapidly than single editing cycles; plus, it has different recognition requirements. This indicates that the editing complex acts in a concerted manner and does not dissociate from the RNA substrate between these cycles. Furthermore, the multicycle substrate exhibits editing that is unexpected from a strictly 3'-to-5' progression, reminiscent of the unexpected editing that has been shown to occur frequently in T. brucei mRNAs edited in vivo. This unexpected editing is most likely due to alternate mRNA:guide RNA (gRNA) alignment forming a hyphenated anchor; its having only a 2-bp proximal duplex helps explain the prevalence of unexpected editing in vivo. Such unexpected editing was not previously reported in vitro, presumably because the common use of artificially tight mRNA:gRNA base pairing precludes alternate alignments. The multicycle editing and unexpected editing presented in this paper bring in vitro reactions closer to reproducing the in vivo editing process.

Indexed as

RNA EditingAnimalsBase Pair MismatchBase SequenceModels, GeneticMolecular Sequence DataProtozoan ProteinsRNA, Guide, KinetoplastidaRNA, MessengerRNA, ProtozoanTrypanosoma brucei bruceiUridineProtozoan ProteinsRNA, Guide, KinetoplastidaRNA, MessengerRNA, ProtozoanUridine

Identifiers

PMID18227152
PMCPMC2268434

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.