Evidence map›Paper›PMID 7493314›Full record

ArticleRNA (New York, N.Y.)1995

In vivo structural analysis of spliced leader RNAs in Trypanosoma brucei and Leptomonas collosoma: a flexible structure that is independent of cap4 methylations.

K A Harris, D M Crothers, E Ullu

Open access · greenAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Probing RNA structure in vivo.Current opinion in structural biology · 2019
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Folding and finding RNA secondary structure.Cold Spring Harbor perspectives in biology · 2010
    Review
  14. Article
  15. Article
  16. Article
  17. Incorporating chemical modification constraints into a dynamic programming algorithm for prediction of RNA secondary structure.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  18. Article
  19. Article
  20. Review
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

3 authors at 1 institution in 1 country.

K A HarrisDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, Connecticut 06520-8114, USA.
D M Crothers
E Ullu
Yale University · US

Funding

TRANSCRIPTION AND RNA PROCESSING IN TRYPANOSOMESR01AI028798 · NIAID · YALE UNIVERSITY · PI TSCHUDI, CHRISTIAN · 1990 to 2020
$10.9M
Nucleic Acid Structure, Dynamics and Protein InteractionR01GM021966 · NIGMS · YALE UNIVERSITY · PI CROTHERS, DONALD M · 1985 to 2009
$3.6M
NUCLEIC ACID STRUCTURE AND PROTEIN INTERACTIONSR37GM021966 · NIGMS · YALE UNIVERSITY · PI CROTHERS, DONALD M · 1992 to 2001
$958k
NIAID NIH HHS AI28798NIGMS NIH HHS GM21966
6 · The paper itself

Abstract

The formation of the mRNA 5' end in trypanosomatid protozoa is carried out by trans-splicing, which transfers a spliced leader (SL) sequence and its hypermethylated cap (cap4) from the SL RNA to the pre-mRNA. Previous in vitro studies with synthetic uncapped RNAs have shown that the SL sequence of Leptomonas collosoma can assume two alternate conformations, Form 1 and Form 2, with Form 1 being the dominant one. To gain information about the structure of the SL RNA in vivo, in its protein-rich environment, we have used permeable Trypanosoma brucei and L. collosoma cells for chemical modification experiments. We introduce the use in vivo of the water-soluble reagents CMCT and kethoxal. In contrast to the in vitro results, the Form 2 secondary structure predominates. However, there are chemically accessible regions that suggest conformational flexibility in SL RNPs and a chemically inaccessible region suggestive of protection by protein or involvement in tertiary interactions. Using complementary 2'-O-methyl RNA oligonucleotides, we show that T. brucei SL RNA can be induced to switch conformation in vivo. SL RNA stripped of proteins and probed in vitro does not display the same Form 2 bias, indicating that SL RNA structure is determined, at least in part, by its RNP context. Finally, the methyl groups of the cap4 do not seem to affect the secondary structure of T. brucei SL RNA, as shown by chemical modification of undermethylated SL RNA probed in vivo.

Indexed as

Nucleic Acid ConformationRNA SplicingAldehydesAnimalsBase SequenceButanonesCell Membrane PermeabilityCME-CarbodiimideCross-Linking ReagentsMethylationMolecular Sequence DataRNA CapsRNA PrecursorsRNA, ProtozoanTrypanosoma brucei bruceiTrypanosomatina1-cyclohexyl-3-(2-(4-morpholinyl)ethyl)carbodiimideAldehydesButanonesCME-CarbodiimideCross-Linking ReagentskethoxalRNA CapsRNA PrecursorsRNA, Protozoan

Identifiers

PMID7493314
PMCPMC1482413
OpenAlexW1767538696

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.