Evidence map›Paper›PMID 21687672›Full record

ArticlePloS one2011

An essential nuclear protein in trypanosomes is a component of mRNA transcription/export pathway.

Mariana Serpeloni, Carolina Borsoi Moraes, João Renato Carvalho Muniz, Maria Cristina Machado Motta, Augusto Savio Peixoto Ramos, Rafael Luis Kessler, Alexandre Haruo Inoue, Wanderson Duarte daRocha, Sueli Fumie Yamada-Ogatta, Stenio Perdigão Fragoso and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  7. Evolution and diversification of the nuclear pore complex.Biochemical Society transactions · 2021
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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

13 authors at 6 institutions in 3 countries.

Mariana SerpeloniDepartamento de Biologia Celular e Molecular, Universidade Federal do Paraná, Curitiba, Brazil.
Carolina Borsoi Moraes
João Renato Carvalho Muniz
Maria Cristina Machado Motta
Augusto Savio Peixoto Ramos
Rafael Luis Kessler
Alexandre Haruo Inoue
Wanderson Duarte daRocha
Sueli Fumie Yamada-Ogatta
Stenio Perdigão Fragoso
Samuel Goldenberg
Lucio H Freitas-Junior
Andréa Rodrigues Avila
Fundação Carlos Chagas · BRInstitut Pasteur Korea · KRUniversidade Estadual de Londrina · BRUniversidade Federal do Paraná · BRUniversidade Federal do Rio de Janeiro · BRUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In eukaryotic cells, different RNA species are exported from the nucleus via specialized pathways. The mRNA export machinery is highly integrated with mRNA processing, and includes a different set of nuclear transport adaptors as well as other mRNA binding proteins, RNA helicases, and NPC-associated proteins. The protozoan parasite Trypanosoma cruzi is the causative agent of Chagas disease, a widespread and neglected human disease which is endemic to Latin America. Gene expression in Trypanosoma has unique characteristics, such as constitutive polycistronic transcription of protein-encoding genes and mRNA processing by trans-splicing. In general, post-transcriptional events are the major points for regulation of gene expression in these parasites. However, the export pathway of mRNA from the nucleus is poorly understood. The present study investigated the function of TcSub2, which is a highly conserved protein ortholog to Sub2/ UAP56, a component of the Transcription/Export (TREX) multiprotein complex connecting transcription with mRNA export in yeast/human. Similar to its orthologs, TcSub2 is a nuclear protein, localized in dispersed foci all over the nuclei -except the fibrillar center of nucleolus- and at the interface between dense and non-dense chromatin areas, proposing the association of TcSub2 with transcription/processing sites. These findings were analyzed further by BrUTP incorporation assays and confirmed that TcSub2 is physically associated with active RNA polymerase II (RNA pol II), but not RNA polymerase I (RNA pol I) or Spliced Leader (SL) transcription, demonstrating participation particularly in nuclear mRNA metabolism in T. cruzi. The double knockout of the TcSub2 gene is lethal in T. cruzi, suggesting it has an essential function. Alternatively, RNA interference assays were performed in Trypanosoma brucei. It allowed demonstrating that besides being an essential protein, its knockdown causes mRNA accumulation in the nucleus and decrease of translation levels, reinforcing that Trypanosoma-Sub2 (Tryp-Sub2) is a component of mRNA transcription/export pathway in trypanosomes.

Indexed as

Transcription, GeneticActive Transport, Cell NucleusAmino Acid SequenceAnimalsCell NucleusCloning, MolecularHumansModels, MolecularMolecular Sequence DataNuclear ProteinsProtein ConformationProtozoan ProteinsRNA, MessengerSequence Homology, Amino AcidTrypanosoma cruziNuclear ProteinsProtozoan ProteinsRNA, Messenger

Identifiers

PMID21687672
PMCPMC3110772
OpenAlexW1964867732

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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.