Medical Journals

N-ethylmaleimide Sensitive Factor is Required for Fusion of the C. Elegans Uterine Anchor Cell.

Authors:
  • Choi Jaebok
  • Richards Keri L
  • Cinar Hediye Nese
  • Newman Anna P

From: Verna and Marrs Maclean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.

Developmental biology

  • Publish Date: Sep 2006
  • ISSN: 0012-1606
  • Volume: 297
  • Issue: 1
  • Pages: 87-102
  • Medium: Print
  • Language: English
  • Citation (JAMA): Choi Jaebok, Richards Keri L, Cinar Hediye Nese, et al. N-ethylmaleimide Sensitive Factor is Required for Fusion of the C. Elegans Uterine Anchor Cell.. Dev. Biol. Sep 2006;297:87-102

Abstract

The fusion of the Caenorhabditis elegans uterine anchor cell (AC) with the uterine-seam cell (utse) is an excellent model system for studying cell-cell fusion, which is essential to animal development. We obtained an egg-laying defective (Egl) mutant in which the AC fails to fuse with the utse. This defect is highly specific: other aspects of utse development and other cell fusions appear to occur normally. We find that defect is due to a missense mutation in the nsf-1 gene, which encodes N-ethylmaleimide-sensitive factor (NSF), an intracellular membrane fusion factor. There are two NSF-1 isoforms, which are expressed in distinct tissues through two separate promoters. NSF-1L is expressed in the uterus, including the AC. We find that nsf-1 is required cell-autonomously in the AC for its fusion with the utse. Our results establish AC fusion as a paradigm for studying cell fusion at single cell resolution and demonstrate that the NSF ATPase is a key player in this process.

Mesh Headings (Keywords): Animals, Animals, Genetically Modified, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cell Fusion, Ethylmaleimide, Female, Membrane Glycoproteins, Mutation, Missense, N-Ethylmaleimide-Sensitive Proteins, Organ Specificity, Phenotype, Promoter Regions (Genetics), Uterus


Check for Full Text / PubMed Unique Identifier (PMID): 16769048


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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