Evidence map›Paper›PMID 16897345›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2006

Identification of genetic variation and putative regulatory regions in bovine CARD15.

Kristen H Taylor, Jeremy F Taylor, Stephen N White, James E Womack

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Polymorphisms in toll-like receptor (Journal of genetics · 2018
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. GSEA-SNP identifies genes associated with Johne's disease in cattle.Mammalian genome : official journal of the International Mammalian Genome Society · 2010
    Article
  8. Article
  9. Risk haplotype analysis for bovine paratuberculosis.Mammalian genome : official journal of the International Mammalian Genome Society · 2009
    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

4 authors at 3 institutions in 1 country.

Kristen H TaylorDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas 77843-4467, USA.
Jeremy F Taylor
Stephen N White
James E Womack
Texas A&M University · USUniversity of Missouri · USWashington State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in caspase recruitment domain 15 (CARD15) are associated with susceptibility to Crohn's disease and Blau Syndrome. We performed comparative analyses of the bovine, murine, and human CARD15 transcripts to elucidate functionality of bovine CARD15 and examine its potential role in bovine disease resistance. Comparative analyses of intronic sequence across seven divergent species were performed to identify putative regulatory element binding motifs. High levels of interspecies conservation in sequence, genomic structure, and protein domains were detected indicating common functionality for CARD15 in cattle, human, and mouse. We identified species-specific regulatory elements in the 5' and 3' untranslated regions, suggesting that modes of regulation may have diverged across species. Thirty-one conserved putative regulatory element binding motifs were identified in the CARD15 intronic sequence of seven species. To assess the extent of genetic diversity within bovine CARD15, 41 individuals from two subspecies were sequenced and screened for polymorphisms. Thirty-six single nucleotide polymorphisms (SNPs) were identified. Finally, 20 subspecies-specific haplotypes were predicted with 7 and 13 unique haplotypes explaining the diversity within B. taurus taurus and B. taurus indicus animals, respectively. Strong evidence for a simple causal relationship between these SNP loci and their haplotypes with Johne's disease was not detected.

Indexed as

Genetic Variation3' Untranslated Regions5' Untranslated RegionsAnimalsCattleChromosome MappingConserved SequenceHaplotypesHumansIntracellular Signaling Peptides and ProteinsMiceNod2 Signaling Adaptor ProteinPolymorphism, Single NucleotideRegulatory Elements, Transcriptional3' Untranslated Regions5' Untranslated RegionsIntracellular Signaling Peptides and ProteinsNOD2 protein, humanNod2 Signaling Adaptor Protein

Identifiers

PMID16897345
OpenAlexW1972343365

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.