Evidence map›Paper›PMID 17651493›Full record

ArticleBMC genomics2007

V1R promoters are well conserved and exhibit common putative regulatory motifs.

Robert Stewart, Robert P Lane

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2007. 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, top 87% of its field
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

The trial behind it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 10 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Robert StewartDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, Connecticut 06459, USA. robstewart2@gmail.com
Robert P Lane
Wesleyan University · US

Funding

Pheromone Receptor Genomic Evolution and Gene RegulationR01DC006267 · NIDCD · WESLEYAN UNIVERSITY · PI LANE, ROBERT P. · 2003 to 2014
$3.6M
NIDCD NIH HHS R01 DC006267NIDCD NIH HHS R01-DC006267
6 · The paper itself

Abstract

backgroundThe mouse vomeronasal organ (VNO) processes chemosensory information, including pheromone signals that influence reproductive behaviors. The sensory neurons of the VNO express two types of chemosensory receptors, V1R and V2R. There are ~165 V1R genes in the mouse genome that have been classified into ~12 divergent subfamilies. Each sensory neuron of the apical compartment of the VNO transcribes only one of the repertoire of V1R genes. A model for mutually exclusive V1R transcription in these cells has been proposed in which each V1R gene might compete stochastically for a single transcriptional complex. This model predicts that the large repertoire of divergent V1R genes in the mouse genome contains common regulatory elements. In this study, we have characterized V1R promoter regions by comparative genomics and by mapping transcription start sites.

resultsWe find that transcription is initiated from ~1 kb promoter regions that are well conserved within V1R subfamilies. While cross-subfamily homology is not evident by traditional methods, we developed a heuristic motif-searching tool, LogoAlign, and applied this tool to identify motifs shared within the promoters of all V1R genes. Our motif-searching tool exhibits rapid convergence to a relatively small number of non-redundant solutions (97% convergence). We also find that the best motifs contain significantly more information than those identified in controls, and that these motifs are more likely to be found in the immediate vicinity of transcription start sites than elsewhere in gene blocks. The best motifs occur near transcription start sites of ~90% of all V1R genes and across all of the divergent subfamilies. Therefore, these motifs are candidate binding sites for transcription factors involved in V1R co-regulation.

conclusionOur analyses show that V1R subfamilies have broad and well conserved promoter regions from which transcription is initiated. Results from a new motif-finding algorithm, LogoAlign, designed for this context and more generally for searching large, hierarchical datasets, suggest the existence of common information-rich regulatory motifs that are shared across otherwise divergent V1R subfamilies.

Indexed as

AlgorithmsAnimalsChemotactic FactorsChromosome MappingChromosomes, MammalianComputational BiologyConserved SequenceDatabases, GeneticGenomeMiceMultigene FamilyPromoter Regions, GeneticRatsReceptors, OdorantRegulatory Sequences, Nucleic AcidTranscription, GeneticChemotactic FactorsReceptors, Odorant

Identifiers

PMID17651493
PMCPMC1955453
OpenAlexW2094031732

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LicenceCC BY
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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.