Evidence map›Paper›PMID 27271303›Full record

ArticlePrimates; journal of primatology2016

Primate genotyping via high resolution melt analysis: rapid and reliable identification of color vision status in wild lemurs.

Rachel L Jacobs, Amanda N Spriggs, Tammie S MacFie, Andrea L Baden, Mitchell T Irwin, Patricia C Wright, Edward E Louis, Richard R Lawler, Nicholas I Mundy, Brenda J Bradley

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Article in Primates; journal of primatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

2 citing papers in PubMed, 9 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

10 authors at 7 institutions in 4 countries.

Rachel L JacobsDepartment of Anthropology, Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC, USA. rachel_jacobs@gwu.edu.
Amanda N SpriggsDepartment of Anthropology, Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC, USA.
Tammie S MacFieDepartment of Zoology, University of Cambridge, Cambridge, UK.
Andrea L BadenCentre ValBio Research Station, Ranomafana, Fianarantsoa, Madagascar.
Mitchell T IrwinDepartment of Anthropology, Northern Illinois University, DeKalb, USA.
Patricia C WrightCentre ValBio Research Station, Ranomafana, Fianarantsoa, Madagascar.
Edward E LouisConservation Genetics Department, Omaha's Henry Doorly Zoo and Aquarium, Omaha, USA.
Richard R LawlerDepartment of Sociology and Anthropology, James Madison University, Harrisonburg, USA.
Nicholas I MundyDepartment of Zoology, University of Cambridge, Cambridge, UK.
Brenda J BradleyDepartment of Anthropology, Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC, USA. bradleyjbrenda@gwu.edu.ORCID http://orcid.org/0000-0002-7084-0385
George Washington University · USUniversity of Cambridge · GBCentre for Conservation and Research · LKJames Madison University · USNorthern Illinois University · USThe Graduate Center, CUNY · USUniversité de Fianarantsoa · MG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analyses of genetic polymorphisms can aid our understanding of intra- and interspecific variation in primate sociality, ecology, and behavior. Studies of primate opsin genes are prime examples of this, as single nucleotide variants (SNVs) in the X-linked opsin gene underlie variation in color vision. For primate species with polymorphic trichromacy, genotyping opsin SNVs can generally indicate whether individual primates are red-green color-blind (denoted homozygous M or homozygous L) or have full trichromatic color vision (heterozygous ML). Given the potential influence of color vision on behavior and fitness, characterizing the color vision status of study subjects is becoming commonplace for many primate field projects. Such studies traditionally involve a multi-step sequencing-based method that can be costly and time-consuming. Here we present a new reliable, rapid, and relatively inexpensive method for characterizing color vision in primate populations using high resolution melt analysis (HRMA). Using lemurs as a case study, we characterized variation at exons 3 and/or 5 of the X-linked opsin gene for 87 individuals representing nine species. We scored opsin genotypes and color vision status using both traditional sequencing-based methods as well as our novel melting-curve based HRMA protocol. For each species, the melting curves of varying genotypes (homozygous M, homozygous L, heterozygous ML) differed in melting temperature and/or shape. Melting curves for each sample were consistent across replicates, and genotype-specific melting curves were consistent across DNA sources (blood vs. feces). We show that opsin genotypes can be quickly and reliably scored using HRMA once lab-specific reference curves have been developed based on known genotypes. Although the protocol presented here focuses on genotyping lemur opsin loci, we also consider the larger potential for applying this approach to various types of genetic studies of primate populations.

Indexed as

Color VisionAnimalsGenotyping TechniquesLemuridaePolymerase Chain ReactionStrepsirhiniOpsinSensory ecologySingle nucleotide variant genotypingStrepsirrhinesTechnique

Identifiers

PMID27271303
OpenAlexW2426328397

What OpenQuestion holds

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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.