Evidence map›Paper›PMID 11713315›Full record

ArticleNucleic acids research2001

Control of DNA excision efficiency in Paramecium.

K Dubrana, L Amar

Abstract read
In one paragraph

Article in Nucleic acids research, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

K DubranaLaboratoire de Génétique Moléculaire, Ecole Normale Supérieure, 46 Rue d'Ulm, 75230 Paris Cedex 05, France.
L Amar

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed excision of internal eliminated sequences (IESs) occurs at thousands of sites in ciliate genomes. How this is controlled is largely unknown. Here, we report the characterization of the non-efficiently excised 156psiG-11 IES from Paramecium primaurelia strain 156 and that of the efficiently excised 168psiG-11 IES, an allelic variant from strain 168. Then, we report a genetic and molecular analysis of IES excision efficiency in F(1) progeny derived from interstrain crosses and in F(2) homozygous progeny derived from F(1) autogamy. IES 168psiG-11 excision efficiency was approximately 100% in all cases. IES 156psiG-11 excision efficiency was 19 +/- 13% in F(1) progeny and 0.6 +/- 1.1% in F(2) progeny. No trans-excision event between IESs 156psiG-11 and 168psiG-11 was detected within the F(1) progeny. These data demonstrate that the excision efficiency of this IES is variable and controlled by a cis-acting element. This should encompass positions 8 and/or 9 of the right IES end, which display allele differences. Finally, the 30-fold stimulation of IES 156psiG-11 excision efficiency within F(1) progeny relative to F(2) progeny demonstrates that Paramecium IES excision efficiency is sensitive either to a conjugation-specific trans-acting factor provided by the zygotic genome, or to homologous chromosome cross-talk.

Indexed as

AllelesAnimalsAntigens, ProtozoanAntigens, SurfaceBase SequenceCell NucleusDNA, ProtozoanGene Expression RegulationMolecular Sequence DataParameciumPseudogenesSequence Analysis, DNASequence Homology, Nucleic AcidAntigens, ProtozoanAntigens, SurfaceDNA, Protozoan

Identifiers

PMID11713315
PMCPMC92537

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.