Expression of the siss-1 gene in C. elegans

<i>C. elegans</i> SISS-1 is an Epidermal Growth Factor (EGF) family ligand that signals from&nbsp;damaged cells to sleep-promoting neurons during s tress- i nduced s leep (SIS). Damage to a range of tissues can trigger SIS, and we reasoned that <i>siss-1</i> should be widely expressed. Here we investigate <i>siss-1</i> expression using both endogenous and transgenic fluorescent reporters. Our endogenous reporter reveals <i>siss-1</i> expression in the pharynx, gut, rectal gland, vulval muscles, and a subset of neurons. Our transgenic reporters reveal expression in additional cell types including the distal tip cell of the migrating gonad and vulF cells of the developing vulva. This expression is specific relative to our expectation and suggests that not all tissues are capable of signaling to sleep neurons.

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Publication Details

Journal
PubMed
Published
2025-12-08
DOI
https://doi.org/10.17912/micropub.biology.001976
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
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article
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article

Expression of the siss-1 gene in C. elegans

Marine Barsegyan, Cheryl Van Buskirk
PubMed
Genetics, Aging, and Longevity in Model Organisms
article

Expression of the siss-1 gene in C. elegans

Marine Barsegyan, Cheryl Van Buskirk
article en

Abstract

<i>C. elegans</i> SISS-1 is an Epidermal Growth Factor (EGF) family ligand that signals from&nbsp;damaged cells to sleep-promoting neurons during s tress- i nduced s leep (SIS). Damage to a range of tissues can trigger SIS, and we reasoned that <i>siss-1</i> should be widely expressed. Here we investigate <i>siss-1</i> expression using both endogenous and transgenic fluorescent reporters. Our endogenous reporter reveals <i>siss-1</i> expression in the pharynx, gut, rectal gland, vulval muscles, and a subset of neurons. Our transgenic reporters reveal expression in additional cell types including the distal tip cell of the migrating gonad and vulF cells of the developing vulva. This expression is specific relative to our expectation and suggests that not all tissues are capable of signaling to sleep neurons.

PubMedVol. 2026
Openalex Percentile: Top 33%
Genetics, Aging, and Longevity in Model Organisms
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