Evidence map›Paper›PMID 42043338›Full record

ReviewGenetics2026

Sevenless: its function and structure in the specification of the Drosophila R7 photoreceptor.

Andrew Tomlinson

Abstract readReview
In one paragraph

Review in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Andrew TomlinsonZuckerman Institute, Department of Genetics and Development, College of Physicians and Surgeons of Columbia University Jerome L. Greene Science Center, Level 9 Room 028, 3227 Broadway, New York, NY 10027, United States.ORCID 0000-0002-3697-6799

Funding

RETINA--THE CONTROL OF PHOTORECEPTOR CELL FATER01EY012536 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TOMLINSON, ANDREW · 1999 to 2011
$4.1M
The Drosophila Ommatidium: a model neural system for cell recruitment and fate specification during developmentR01EY030956 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TOMLINSON, ANDREW · 2020 to 2024
$1.6M
Receptor Tyrosine Kinase Activity in Drosophila Eye DevelopmentR01EY026217 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TOMLINSON, ANDREW · 2016 to 2019
$1.3M
NEI NIH HHS R01 EY012536NEI NIH HHS R01 EY026217NEI NIH HHS R01 EY030956
6 · The paper itself

Abstract

The fly eye is composed of hundreds of ommatidia, each containing a stereotyped pattern of photoreceptors and assorted support cells. Over the past 50 years, molecular genetic studies have illuminated how the fates of many of these cells are specified. As a result, the field has become a classic paradigm for cell-fate specification during animal development. The initial focus of the studies was the sevenless (sev) mutant, in which the cell normally destined to become the R7 photoreceptor instead develops into a lens-secreting support cell. This phenotype served as the entry point into the patterning mechanisms underlying ommatidial fate specification. sev was found to encode a receptor tyrosine kinase (RTK) expressed on the plasma membrane of the R7 precursor. Its ligand-Bride of Sevenless (Boss)-was then identified as a plasma membrane protein expressed on a neighboring cell, the presumptive R8 photoreceptor. Here, I present a personal perspective on the studies of Sev, from its discovery to the present day, beginning with the characterization of its loss-of-function phenotype and culminating in the highly detailed description of its biological role and the molecular mechanism by which it transduces the R8-to-R7 Boss signal. These studies have revealed surprisingly complex and novel properties of this seemingly simple signaling mechanism, including (i) the unexpected circuitry by which Sev signaling is integrated with that of the Drosophila EGF receptor and Notch to specify 3 distinct cell types (R7 and R1/6 photoreceptors and the lens-secreting cone cells) and (ii) the likely discovery of a new molecular mechanism of RTK activation in which transendocytosis of Boss from the presumptive R8 into the R7 precursor directs Sev to a select endocytic compartment, where it is activated by a conformation state induced by low pH. Further, I address evolutionary studies of Sev and Boss, which indicate that their roles as ligand and receptor are restricted to flies, and pose the intriguing question of whether R7 photoreceptors outside Diptera are specified by similar signaling logic but different molecular machinery.

Indexed as

DrosophilaDrosophila ProteinsPhotoreceptor Cells, InvertebrateAnimalsEye ProteinsMembrane ProteinsReceptor Protein-Tyrosine KinasesSignal TransductionDrosophila ProteinsEye ProteinsMembrane ProteinsReceptor Protein-Tyrosine Kinasessev protein, Drosophilacell-cell communicationdevelopmentDrosophila eyepattern formationreceptor tyrosine kinasesevenless

Identifiers

PMID42043338
PMCPMC13232746

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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.