Evidence map›Paper›PMID 18394580›Full record

ArticleAmerican journal of human genetics2008

Mapping of small RNAs in the human ENCODE regions.

Christelle Borel, Maryline Gagnebin, Corinne Gehrig, Evgenia V Kriventseva, Evgeny M Zdobnov, Stylianos E Antonarakis

Abstract read
In one paragraph

Article in American journal of human genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Reply to Verwilt et al.: Experimental evidence against DNA contamination in SILVER-seq.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. The association between H3K4me3 and antisense transcription.Genomics, proteomics & bioinformatics · 2012
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Regulatory roles of natural antisense transcripts.Nature reviews. Molecular cell biology · 2009
    Review
  12. Article
  13. Review
  14. Review
  15. Noncoding RNA in development.Mammalian genome : official journal of the International Mammalian Genome Society · 2008
    Review
  16. Article
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

6 authors.

Christelle BorelDepartment of Genetic Medicine and Development, University of Geneva Medical School and University Hospitals of Geneva, Geneva 1211, Switzerland.
Maryline Gagnebin
Corinne Gehrig
Evgenia V Kriventseva
Evgeny M Zdobnov
Stylianos E Antonarakis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The elucidation of the largely unknown transcriptome of small RNAs is crucial for the understanding of genome and cellular function. We report here the results of the analysis of small RNAs (< 50 nt) in the ENCODE regions of the human genome. Size-fractionated RNAs from four different cell lines (HepG2, HelaS3, GM06990, SK-N-SH) were mapped with the forward and reverse ENCODE high-density resolution tiling arrays. The top 1% of hybridization signals are termed SmRfrags (Small RNA fragments). Eight percent of SmRfrags overlap the GENCODE genes (CDS), given that the majority map to intergenic regions (34%), intronic regions (53%), and untranslated regions (UTRs) (5%). In addition, 9.6% and 16.8% of SmRfrags in the 5' UTR regions overlap significantly with His/Pol II/TAF250 binding sites and DNase I Hypersensitive sites, respectively (compared to the 5.3% and 9% expected). Interestingly, 17%-24% (depending on the cell line) of SmRfrags are sense-antisense strand pairs that show evidence of overlapping transcription. Only 3.4% and 7.2% of SmRfrags in intergenic regions overlap transcribed fragments (Txfrags) in HeLa and GM06990 cell lines, respectively. We hypothesized that a fraction of the identified SmRfrags corresponded to microRNAs. We tested by Northern blot a set of 15 high-likelihood predictions of microRNA candidates that overlap with smRfrags and validated three potential microRNAs ( approximately 20 nt length). Notably, most of the remaining candidates showed a larger hybridizing band ( approximately 100 nt) that could be a microRNA precursor. The small RNA transcriptome is emerging as an important and abundant component of the genome function.

Indexed as

Chromosome MappingTranscription, Genetic5' Untranslated RegionsBase SequenceCell Line, TumorGenome, HumanHumansMicroRNAsMolecular Sequence DataOligonucleotide Array Sequence Analysis5' Untranslated RegionsMicroRNAs

Identifiers

PMID18394580
PMCPMC2427294

What OpenQuestion holds

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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.