Evidence map›Paper›PMID 26733090›Full record

ArticleBMC molecular biology2016

Structural and functional analysis of four non-coding Y RNAs from Chinese hamster cells: identification, molecular dynamics simulations and DNA replication initiation assays.

Quirino Alves de Lima Neto, Francisco Ferreira Duarte Junior, Paulo Sérgio Alves Bueno, Flavio Augusto Vicente Seixas, Madzia Pauline Kowalski, Eyemen Kheir, Torsten Krude, Maria Aparecida Fernandez

Open access · hybridAbstract read
In one paragraph

Article in BMC molecular biology, 2016. 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, top 100% 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

0 citing papers in PubMed, 9 citations in OpenAlex.

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

8 authors at 2 institutions in 2 countries.

Quirino Alves de Lima NetoDepartamento de Biotecnologia, Genética e Biologia Celular, Universidade Estadual de Maringá, Av. Colombo 5790, Maringá, Paraná, 87020-900, Brazil. qalneto@gmail.com.
Francisco Ferreira Duarte JuniorDepartamento de Biotecnologia, Genética e Biologia Celular, Universidade Estadual de Maringá, Av. Colombo 5790, Maringá, Paraná, 87020-900, Brazil. junior.fduarte@gmail.com.
Paulo Sérgio Alves BuenoDepartamento de Bioquímica, Universidade Estadual de Maringá, UEM, Paraná, 87020-900, Brazil. psabueno@gmail.com.
Flavio Augusto Vicente SeixasDepartamento de Bioquímica, Universidade Estadual de Maringá, UEM, Paraná, 87020-900, Brazil. favseixas@gmail.com.
Madzia Pauline KowalskiDepartment of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK. mpcross@stanford.edu.
Eyemen KheirDepartment of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK. eyemen.kheir@gmail.com.
Torsten KrudeDepartment of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK. tk218@cam.ac.uk.
Maria Aparecida FernandezDepartamento de Biotecnologia, Genética e Biologia Celular, Universidade Estadual de Maringá, Av. Colombo 5790, Maringá, Paraná, 87020-900, Brazil. aparecidafernandez@gmail.com.
Universidade Estadual de Maringá · BRUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F016581/1Worldwide Cancer Research 10-0570
6 · The paper itself

Abstract

backgroundThe genes coding for Y RNAs are evolutionarily conserved in vertebrates. These non-coding RNAs are essential for the initiation of chromosomal DNA replication in vertebrate cells. However thus far, no information is available about Y RNAs in Chinese hamster cells, which have already been used to detect replication origins and alternative DNA structures around these sites. Here, we report the gene sequences and predicted structural characteristics of the Chinese hamster Y RNAs, and analyze their ability to support the initiation of chromosomal DNA replication in vitro.

resultsWe identified DNA sequences in the Chinese hamster genome of four Y RNAs (chY1, chY3, chY4 and chY5) with upstream promoter sequences, which are homologous to the four main types of vertebrate Y RNAs. The chY1, chY3 and chY5 genes were highly conserved with their vertebrate counterparts, whilst the chY4 gene showed a relatively high degree of diversification from the other vertebrate Y4 genes. Molecular dynamics simulations suggest that chY4 RNA is structurally stable despite its evolutionarily divergent predicted stem structure. Of the four Y RNA genes present in the hamster genome, we found that only the chY1 and chY3 RNA were strongly expressed in the Chinese hamster GMA32 cell line, while expression of the chY4 and chY5 RNA genes was five orders of magnitude lower, suggesting that they may in fact not be expressed. We synthesized all four chY RNAs and showed that any of these four could support the initiation of DNA replication in an established human cell-free system.

conclusionsThese data therefore establish that non-coding chY RNAs are stable structures and can substitute for human Y RNAs in a reconstituted cell-free DNA replication initiation system. The pattern of Y RNA expression and functionality is consistent with Y RNAs of other rodents, including mouse and rat.

Indexed as

DNA ReplicationMolecular Dynamics SimulationNucleic Acid ConformationAnimalsCell LineComputer SimulationCricetulusGene Expression RegulationGenomeHydrogen BondingModels, MolecularRNA, UntranslatedStructure-Activity RelationshipRNA, Untranslated

Identifiers

PMID26733090
PMCPMC4702372
OpenAlexW2226907971

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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.