Evidence map›Paper›PMID 38605281›Full record

ArticlePrimates; journal of primatology2024

Reduction of bitter taste receptor gene family in folivorous colobine primates relative to omnivorous cercopithecine primates.

Min Hou, Muhammad Shoaib Akhtar, Masahiro Hayashi, Ryuichi Ashino, Akiko Matsumoto-Oda, Takashi Hayakawa, Takafumi Ishida, Amanda D Melin, Hiroo Imai, Shoji Kawamura

Open access · hybridAbstract read
In one paragraph

Article in Primates; journal of primatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Bitter taste receptors.Chemical senses · 2025
    Review
  3. Review
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 5 institutions in 2 countries.

Min HouDepartment of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience BLDG Room 502, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 277-8562, Japan.
Muhammad Shoaib AkhtarDepartment of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience BLDG Room 502, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 277-8562, Japan.
Masahiro HayashiDepartment of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience BLDG Room 502, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 277-8562, Japan.
Ryuichi AshinoDepartment of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience BLDG Room 502, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 277-8562, Japan.
Akiko Matsumoto-OdaGraduate School of Tourism Sciences, University of the Ryukyus, Nishihara, Okinawa, Japan.
Takashi HayakawaFaculty of Environmental Earth Science, Hokkaido University, Sapporo, Hokkaido, Japan.
Takafumi IshidaDepartment of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Amanda D MelinDepartment of Anthropology and Archaeology, University of Calgary, Alberta, Canada.
Hiroo ImaiMolecular Biology Section, Center for the Evolutionary Origins of Human Behavior, Kyoto University, Kyoto, Aichi, Japan.
Shoji KawamuraDepartment of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience BLDG Room 502, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 277-8562, Japan. kawamura@edu.k.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0003-0350-6050
The University of Tokyo · JPHokkaido University · JPKyoto University · JPUniversity of Calgary · CAUniversity of the Ryukyus · JP

Funding

Canada Research Chairs 950-231257Cooperative Research Program of the Primate Research Institute of Kyoto University 2012-A-11Cooperative Research Program of the Primate Research Institute of Kyoto University 2020-A-27Cooperative Research Program of the Primate Research Institute of Kyoto University grants 2021-A-25Japan Society for the Promotion of Science 15H02421Japan Society for the Promotion of Science 18H04005Japan Society for the Promotion of Science 22H02674Japan Society for the Promotion of Science 23405016Japan Society for the Promotion of Science 23H02561National Sciences and Engineering Research Council of Canada RGPIN-2017-03782
6 · The paper itself

Abstract

Bitter taste perception is important in preventing animals from ingesting potentially toxic compounds. Whole-genome assembly (WGA) data have revealed that bitter taste receptor genes (TAS2Rs) comprise a multigene family with dozens of intact and disrupted genes in primates. However, publicly available WGA data are often incomplete, especially for multigene families. In this study, we employed a targeted capture (TC) approach specifically probing TAS2Rs for ten species of cercopithecid primates with diverse diets, including eight omnivorous cercopithecine species and two folivorous colobine species. We designed RNA probes for all TAS2Rs that we modeled to be intact in the common ancestor of cercopithecids ("ancestral-cercopithecid TAS2R gene set"). The TC was followed by short-read and high-depth massive-parallel sequencing. TC retrieved more intact TAS2R genes than found in WGA databases. We confirmed a large number of gene "births" at the common ancestor of cercopithecids and found that the colobine common ancestor and the cercopithecine common ancestor had contrasting trajectories: four gene "deaths" and three gene births, respectively. The number of intact TAS2R genes was markedly reduced in colobines (25-28 detected via TC and 20-26 detected via WGA analysis) as compared with cercopithecines (27-36 via TC and 19-30 via WGA). Birth or death events occurred at almost every phylogenetic-tree branch, making the composition of intact genes variable among species. These results show that evolutionary change in intact TAS2R genes is a complex process, refute a simple general prediction that herbivory favors more TAS2R genes, and have implications for understanding dietary adaptations and the evolution of detoxification abilities.

Indexed as

ColobinaeReceptors, G-Protein-CoupledAnimalsCercopithecidaeDietEvolution, MolecularMultigene FamilyPhylogenyTasteTaste Receptors, Type 2Receptors, G-Protein-CoupledTaste Receptors, Type 2Birth and death evolutionCercopithecinesColobinesPhylogeny-based probe designTargeted captureTAS2R

Identifiers

PMID38605281
PMCPMC11219393
OpenAlexW4394710918

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.