Evidence map›Paper›PMID 21717223›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2011

Transcriptional variations mediated by an alternative promoter of the FPR3 gene.

Hong-Seok Ha, Jae-Won Huh, Jeong-An Gim, Kyudong Han, Heui-Soo Kim

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Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

4 citing papers in PubMed.

  1. Review
  2. Aberrant DNA methylation levels of theAmerican journal of translational research · 2020
    Article
  3. Article
  4. Article
4 · The record

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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

5 authors.

Hong-Seok HaDepartment of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 609-735, Republic of Korea.
Jae-Won Huh
Jeong-An Gim
Kyudong Han
Heui-Soo Kim

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formyl peptide receptor 3 (FPR3) is a potential player in innate immunity and appears with FPR2 as a FPR cluster during primate evolution. Comparative genome analyses indicate that a segmental duplication (SD) event upstream of the FPR3 gene after the divergence of New and Old World monkeys led to the emergence of an alternative promoter. In this study we combined computational and experimental approaches to identify a FPR3 gene that is controlled by an alternative promoter derived during a SD event. Its transcriptional activity was detected by quantitative reverse transcription polymerase chain reaction. Human alternative transcripts (FPR3-1 and FPR3-2) showed tissue-specific patterns with strong expressions in lung or uterus, while the FPR3-1 transcript of rhesus macaque is broadly expressed in various tissues. Overall, transcriptional variations of FPR3 occur by an alternative promoter during primate evolution.

Indexed as

Promoter Regions, GeneticTranscription, GeneticAnimalsBase SequenceCell Line, TumorEvolution, MolecularGene Expression ProfilingGene OrderHeLa CellsHumansMolecular Sequence DataPhylogenyPrimatesReceptors, Formyl PeptideSegmental Duplications, GenomicFPR3 protein, humanReceptors, Formyl Peptide

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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.