Evidence map›Paper›PMID 35294865›Full record

ArticleCurrent biology : CB2022

Ir56b is an atypical ionotropic receptor that underlies appetitive salt response in Drosophila.

Hany K M Dweck, Gaëlle J S Talross, Yichen Luo, Shimaa A M Ebrahim, John R Carlson

Abstract read
In one paragraph

Article in Current biology : CB, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
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

34 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Insulin and leucokinin pathways coordinate adaptive salt appetite inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Stress-induced preference for antioxidants byProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Single-Sensillum Taste Recordings in Mosquitoes.Cold Spring Harbor protocols · 2024
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Hany K M DweckDepartment Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Gaëlle J S TalrossDepartment Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Yichen LuoDepartment Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Shimaa A M EbrahimDepartment Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
John R CarlsonDepartment Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA. Electronic address: john.carlson@yale.edu.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
ANALYSIS OF ODORANT RECEPTOR GENESR01DC004729 · NIDCD · YALE UNIVERSITY · PI John R Carlson · 2001 to 2026
$9.2M
GENETIC AND MOLECULAR ANALYSIS OF OLFACTIONR01DC002174 · NIDCD · YALE UNIVERSITY · PI CARLSON, JOHN R · 1994 to 2024
$8.0M
Analysis of a large family of taste receptorsR01DC011697 · NIDCD · YALE UNIVERSITY · PI John R Carlson · 2011 to 2026
$5.5M
Molecular basis of olfaction in Tsetse flyF32DC018445 · NIDCD · YALE UNIVERSITY · PI EBRAHIM, SHIMAA ABDELSALAM MOHAMED · 2020 to 2022
$218k
Non-coding RNA in the olfactory system of DrosophilaF32DC019302 · NIDCD · YALE UNIVERSITY · PI TALROSS, GAËLLE J.S. · 2021 to 2023
$181k
NCATS NIH HHS UL1 TR001863NIDCD NIH HHS F32 DC018445NIDCD NIH HHS F32 DC019302NIDCD NIH HHS R01 DC002174NIDCD NIH HHS R01 DC004729NIDCD NIH HHS R01 DC011697
6 · The paper itself

Abstract

Salt taste is one of the most ancient of all sensory modalities. However, the molecular basis of salt taste remains unclear in invertebrates. Here, we show that the response to low, appetitive salt concentrations in Drosophila depends on Ir56b, an atypical member of the ionotropic receptor (Ir) family. Ir56b acts in concert with two coreceptors, Ir25a and Ir76b. Mutation of Ir56b virtually eliminates an appetitive behavioral response to salt. Ir56b is expressed in neurons that also sense sugars via members of the Gr (gustatory receptor) family. Misexpression of Ir56b in bitter-sensing neurons confers physiological responses to appetitive doses of salt. Ir56b is unique among tuning Irs in containing virtually no N-terminal region, a feature that is evolutionarily conserved. Moreover, Ir56b is a "pseudo-pseudogene": its coding sequence contains a premature stop codon that can be replaced with a sense codon without loss of function. This stop codon is conserved among many Drosophila species but is absent in a number of species associated with cactus in arid regions. Thus, Ir56b serves the evolutionarily ancient function of salt detection in neurons that underlie both salt and sweet taste modalities.

Indexed as

DrosophilaDrosophila ProteinsAnimalsDrosophila melanogasterSodium ChlorideTasteTaste PerceptionDrosophila ProteinsSodium ChlorideDrosophilaionotropic receptorsIr56bpseudo-pseudogenesalt tastesugar-sensing neurons

Identifiers

PMID35294865
PMCPMC9050924

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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.