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A multi-layered and dynamic apical extracellular matrix shapes the vulva lumen in Caenorhabditis elegans.

Jennifer D Cohen | Alessandro P Sparacio | Alexandra C Belfi | Rachel Forman-Rubinsky | David H Hall | Hannah Maul-Newby | Alison R Frand | Meera V Sundaram
eLife | 2020

Biological tubes must develop and maintain their proper diameter to transport materials efficiently. These tubes are molded and protected in part by apical extracellular matrices (aECMs) that line their lumens. Despite their importance, aECMs are difficult to image in vivo and therefore poorly understood. The Caenorhabditis elegans vulva has been a paradigm for understanding many aspects of organogenesis. Here we describe the vulva luminal matrix, which contains chondroitin proteoglycans, Zona Pellucida (ZP) domain proteins, and other glycoproteins and lipid transporters related to those in mammals. Confocal and transmission electron microscopy revealed, with unprecedented detail, a complex and dynamic aECM. Different matrix factors assemble on the apical surfaces of each vulva cell type, with clear distinctions seen between Ras-dependent (1°) and Notch-dependent (2°) cell types. Genetic perturbations suggest that chondroitin and other aECM factors together generate a structured scaffold that both expands and constricts lumen shape.

Pubmed ID: 32975517

Associated grants

  • Agency: NIH HHS, United States
    Id: R24 OD010943
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM136315
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM008216
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM125959
  • Agency: NIAMS NIH HHS, United States
    Id: T32 AR007465
  • Agency: American Cancer Society, International
    Id: RSG-12-149-01-DDC
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM058540
  • Agency: NIH HHS, United States
    Id: P40 OD010440

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PRISM (tool)

RRID:SCR_005375

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 5,2022.Tool that predicts interactions between transcription factors and their regulated genes from binding motifs. Understanding vertebrate development requires unraveling the cis-regulatory architecture of gene regulation. PRISM provides accurate genome-wide computational predictions of transcription factor binding sites for the human and mouse genomes, and integrates the predictions with GREAT to provide functional biological context. Together, accurate computational binding site prediction and GREAT produce for each transcription factor: 1. putative binding sites, 2. putative target genes, 3. putative biological roles of the transcription factor, and 4. putative cis-regulatory elements through which the factor regulates each target in each functional role.

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