Evidence map›Paper›PMID 23244605›Full record

ArticleBMC genomics2012

Identification of 3' gene ends using transcriptional and genomic conservation across vertebrates.

Marcos Morgan, Alessandra Iaconcig, Andrés Fernando Muro

Abstract read
In one paragraph

Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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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

3 authors.

Marcos MorganInternational Centre for Genetic Engineering and Biotechnology (ICGEB), Padriciano 99, I 34149, Trieste, Italy. marcos.morgan@embl.it
Alessandra Iaconcig
Andrés Fernando Muro

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn higher eukaryotes, gene expression is regulated at different levels. In particular, 3'UTRs play a central role in translation, stability and subcellular localization of transcripts. In recent years, the development of high throughput sequencing techniques has facilitated the acquisition of transcriptional data at a genome wide level. However, annotation of the 3' ends of genes is still incomplete, thus limiting the interpretation of the data generated. For example, we have previously reported two different genes, ADD2 and CPEB3, with conserved 3'UTR alternative isoforms not annotated in the current versions of Ensembl and RefSeq human databases.

resultsIn order to evaluate the existence of other conserved 3' ends not annotated in these databases we have now used comparative genomics and transcriptomics across several vertebrate species. In general, we have observed that 3'UTR conservation is lost after the end of the mature transcript. Using this change in conservation before and after the 3' end of the mature transcripts we have shown that many conserved ends were still not annotated. In addition, we used orthologous transcripts to predict 3'UTR extensions and validated these predictions using total RNA sequencing data. Finally, we used this method to identify not annotated 3' ends in rats and dogs. As a result, we report several hundred novel 3'UTR extensions in rats and a few thousand in dogs.

conclusionsThe methods presented here can efficiently facilitate the identification of not-yet-annotated conserved 3'UTR extensions. The application of these methods will increase the confidence of orthologous gene models across vertebrates.

Indexed as

Genomics3' Untranslated RegionsAnimalsConserved SequenceDatabases, GeneticDogsExpressed Sequence TagsHumansPolyadenylationRatsSequence Homology, Nucleic AcidTranscription, GeneticVertebrates3' Untranslated Regions

Identifiers

PMID23244605
PMCPMC3564943

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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.