Distinct requirements for the <i>C. elegans</i> Delta ligand APX-1 in embryonic viability and adult fertility

Requirements for the Caenorhabditis elegans Notch ligand APX-1 have been described, but the molecular lesions in mutant alleles remain unknown. Here we report the sequence changes in 3 previously isolated nonconditional alleles and 2 newly isolated alleles, apx-1(or545ts) and a null allele apx-1(or2015). All alleles resulted in highly penetrant embryonic lethality, but only null mutations greatly reduced brood sizes. This reproductive phenotype was likely due to abnormal ovulation rupturing oocytes and, together with vulva defects, resulting in debris accumulation that prevented embryo passage. In addition to identifying molecular lesions in apx-1 alleles and clarifying distinct requirements for C. elegans Notch ligands, our results reveal extensive genotype-by-environment interactions, including haplo-insufficiency of essential loci at a stressfully high growth temperature, and highlight the origins of complex phenotypes as a consequence of multiple seemingly unrelated defects.

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Publication Details

Journal
G3 Genes Genomes Genetics
Published
2025-09-26
DOI
https://doi.org/10.1093/g3journal/jkaf229
Citations
1
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.95

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article

Distinct requirements for the C. elegans Delta ligand APX-1 in embryonic viability and adult fertility

Bruce Bowerman, Ilya Ruvinsky, Erin Z. Aprison, Chien-Hui Chuang
1 citations
G3 Genes Genomes Genetics
Genetics, Aging, and Longevity in Model Organisms
0.95
article

Distinct requirements for the C. elegans Delta ligand APX-1 in embryonic viability and adult fertility

Bruce Bowerman, Ilya Ruvinsky, Erin Z. Aprison, Chien-Hui Chuang
article en
1 citations

Abstract

Requirements for the Caenorhabditis elegans Notch ligand APX-1 have been described, but the molecular lesions in mutant alleles remain unknown. Here we report the sequence changes in 3 previously isolated nonconditional alleles and 2 newly isolated alleles, apx-1(or545ts) and a null allele apx-1(or2015). All alleles resulted in highly penetrant embryonic lethality, but only null mutations greatly reduced brood sizes. This reproductive phenotype was likely due to abnormal ovulation rupturing oocytes and, together with vulva defects, resulting in debris accumulation that prevented embryo passage. In addition to identifying molecular lesions in apx-1 alleles and clarifying distinct requirements for C. elegans Notch ligands, our results reveal extensive genotype-by-environment interactions, including haplo-insufficiency of essential loci at a stressfully high growth temperature, and highlight the origins of complex phenotypes as a consequence of multiple seemingly unrelated defects.

G3 Genes Genomes GeneticsVol. 15(12)
Northwestern University (US), Oregon Research Institute (US), University of Oregon (US)
National Institutes of Health, Medical Research Council, Biotechnology and Biological Sciences Research Council, National Human Genome Research Institute, National Institute of General Medical Sciences
Openalex Percentile: Top 23%
Genetics, Aging, and Longevity in Model Organisms
0.95
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Distinct requirements for the <i>C. elegans</i> Delta ligand APX-1 in embryonic viability and adult fertility — Bruce Bowerman, Ilya Ruvinsky, et al. · G3 Genes Genomes Genetics (2025) | TGRS Research Map | TGRS