TY - JOUR
T1 - Targeting the cell membrane in established and emerging model organisms
AU - Karapidaki, Irene
AU - Handberg-Thorsager, Mette
AU - Momose, Tsuyoshi
AU - Yasuo, Hitoyoshi
AU - Genikhovich, Grigory
AU - Assaf, Sarah
AU - Deleau, Clara
AU - Pang, Ying
AU - Pavlich, Clayton
AU - Lohmann, Beke
AU - Rusciano, Maria Lorenza
AU - Stranges, Mattia
AU - Mathieu, Juliette
AU - Zilliox, Marie
AU - Ustyantsev, Kirill
AU - Salmon, Bastien
AU - Laplace-Builhé, Béryl
AU - Koenig, Manon
AU - Colgren, Jeffrey J
AU - Berezikov, Eugene
AU - Brunet, Thibaut
AU - Bucher, Gregor
AU - Burkhardt, Pawel
AU - Dickinson, Daniel J
AU - Huisken, Jan
AU - Leclère, Lucas
AU - Arnone, Maria Ina
AU - Houliston, Evelyn
AU - Averof, Michalis
N1 - © 2026. Published by The Company of Biologists.
PY - 2026/4/15
Y1 - 2026/4/15
N2 - Transgenic markers and tools have revolutionised how we study cells and developing organisms. Some elements needed to construct those tools are universally applicable (e.g. fluorescent proteins), while others are species specific (e.g. cis-regulatory elements driving transcription). Membrane-localising signals that target proteins to the plasma membrane have been identified in some organisms, but their efficacy varies across species. To address this problem, we generated a toolkit of 11 membrane-localising tags that can be screened rapidly in diverse organisms. The toolkit includes tags targeting the plasma membrane through different mechanisms, including signal peptides, lipid attachments or fusion with lipid-binding domains. Each tag was fused to the fluorescent protein mScarlet3 and placed downstream of a T7 promoter, to produce mRNA that can be delivered in a wide range of embryos and cells. Through a collaborative effort, we tested this toolkit in ten animals spanning diverse phyla, including chordates, echinoderms, arthropods, nematodes, annelids, flatworms and cnidarians. We identify robust membrane-localising tags in each of these animals, and in the animals' closest relatives, the choanoflagellates. Three tags (KRas, GAP43 and Src64B) work in all the species we tested.
AB - Transgenic markers and tools have revolutionised how we study cells and developing organisms. Some elements needed to construct those tools are universally applicable (e.g. fluorescent proteins), while others are species specific (e.g. cis-regulatory elements driving transcription). Membrane-localising signals that target proteins to the plasma membrane have been identified in some organisms, but their efficacy varies across species. To address this problem, we generated a toolkit of 11 membrane-localising tags that can be screened rapidly in diverse organisms. The toolkit includes tags targeting the plasma membrane through different mechanisms, including signal peptides, lipid attachments or fusion with lipid-binding domains. Each tag was fused to the fluorescent protein mScarlet3 and placed downstream of a T7 promoter, to produce mRNA that can be delivered in a wide range of embryos and cells. Through a collaborative effort, we tested this toolkit in ten animals spanning diverse phyla, including chordates, echinoderms, arthropods, nematodes, annelids, flatworms and cnidarians. We identify robust membrane-localising tags in each of these animals, and in the animals' closest relatives, the choanoflagellates. Three tags (KRas, GAP43 and Src64B) work in all the species we tested.
KW - Animals
KW - Cell Membrane/metabolism
KW - Animals, Genetically Modified
U2 - 10.1242/dev.205415
DO - 10.1242/dev.205415
M3 - Article
C2 - 41995178
SN - 0950-1991
VL - 153
JO - DEVELOPMENT
JF - DEVELOPMENT
IS - 8
ER -