Evidence map›Paper›PMID 37481261›Full record

ArticleG3 (Bethesda, Md.)2023

Chromosome-level reference genome for North American bison (Bison bison) and variant database aids in identifying albino mutation.

Sam Stroupe, Carly Martone, Blake McCann, Rytis Juras, Helena Josefina Kjöllerström, Terje Raudsepp, Donald Beard, Brian W Davis, James N Derr

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2023. 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
1.7field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Methylation-associated mutagenesis underlies variation in the mutation spectrum across eukaryotes.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

9 authors at 3 institutions in 1 country.

Sam StroupeDepartment of Veterinary Pathobiology, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
Carly MartoneDepartment of Veterinary Pathobiology, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
Blake McCannNational Park Service, Theodore Roosevelt National Park, Medora, ND 58645, USA.
Rytis JurasDepartment of Veterinary Integrative Biosciences, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
Helena Josefina KjöllerströmDepartment of Veterinary Integrative Biosciences, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
Terje RaudseppDepartment of Veterinary Integrative Biosciences, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
Donald BeardTexas Parks and Wildlife, Caprock Canyons State Park & Trailway, Quitaque, TX 79255, USA.
Brian W DavisDepartment of Veterinary Integrative Biosciences, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
James N DerrDepartment of Veterinary Pathobiology, Texas A&M University School of Veterinary Medicine and Biomedical Science, College Station, TX 77843, USA.
Texas A&M University · USNational Park Service · USTexas Parks and Wildlife Department · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We developed a highly contiguous chromosome-level reference genome for North American bison to provide a platform to evaluate the conservation, ecological, evolutionary, and population genomics of this species. Generated from a F1 hybrid between a North American bison dam and a domestic cattle bull, completeness and contiguity exceed that of other published bison genome assemblies. To demonstrate the utility for genome-wide variant frequency estimation, we compiled a genomic variant database consisting of 3 true albino bison and 44 wild-type pelage color bison. Through the examination of genomic variants fixed in the albino cohort and absent in the controls, we identified a nonsynonymous single nucleotide polymorphism (SNP) mutation on chromosome 29 in exon 3 of the tyrosinase gene (c.1114C>T). A TaqMan SNP Genotyping Assay was developed to genotype this SNP in a total of 283 animals across 29 herds. This assay confirmed the absence of homozygous variants in all animals except 7 true albino bison included in this study. In addition, the only heterozygous animals identified were 2 wild-type pelage color dams of albino offspring. Therefore, we propose that this new high-quality bison genome assembly and incipient variant database provides a highly robust and informative resource for genomics investigations for this iconic North American species.

Indexed as

BisonAnimalsCattleChromosomesGenomeMutationNorth Americaalbinismbison reference genomegenome variant databasegenomicsNorth American bisontyrosinase gene

Identifiers

PMID37481261
PMCPMC10542314
OpenAlexW4385071369

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.