Computational insights into Caenorhabditis elegans vulval development. Fisher, J., Piterman, N., Hubbard, Stern, M. J., & Harel, D. Proceedings of the National Academy of Sciences of the United States of America, 102(6):1951–1956, Department of Computer Science and Applied Mathematics, Weizmann Institute of Science, Rehovot 76100, Israel. jasmine.fixher@weizmann.ac.il, February, 2005.
Computational insights into Caenorhabditis elegans vulval development [link]Paper  doi  abstract   bibtex   
Studies of Caenorhabditis elegans vulval development provide a paradigm for pattern formation during animal development. The fates of the six vulval precursor cells are specified by the combined action of an inductive signal that activates the EGF receptor mitogen-activated PK signaling pathway (specifying a primary fate) and a lateral signal mediated by LIN-12/Notch (specifying a secondary fate). Here we use methods devised for the engineering of complex reactive systems to model a biological system. We have chosen the visual formalism of statecharts and use it to formalize Sternberg and Horvitz's 1989 model [Sternberg, P. W. & Horvitz, H. R. (1989) Cell 58, 679–693], which forms the basis for our current understanding of the interaction between these two signaling pathways. The construction and execution of our model suggest that different levels of the inductive signal induce a temporally graded response of the EGF receptor mitogen-activated PK pathway and make explicit the importance of this temporal response. Our model also suggests the existence of an additional mechanism operating during lateral specification that prohibits neighboring vulval precursor cells from assuming the primary fate.
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  abstract = {Studies of Caenorhabditis elegans vulval development provide a paradigm for pattern formation during animal development. The fates of the six vulval precursor cells are specified by the combined action of an inductive signal that activates the {EGF} receptor mitogen-activated {PK} signaling pathway (specifying a primary fate) and a lateral signal mediated by {LIN}-{12/Notch} (specifying a secondary fate). Here we use methods devised for the engineering of complex reactive systems to model a biological system. We have chosen the visual formalism of statecharts and use it to formalize Sternberg and Horvitz's 1989 model [Sternberg, P. W. \& Horvitz, H. R. (1989) Cell 58, 679–693], which forms the basis for our current understanding of the interaction between these two signaling pathways. The construction and execution of our model suggest that different levels of the inductive signal induce a temporally graded response of the {EGF} receptor mitogen-activated {PK} pathway and make explicit the importance of this temporal response. Our model also suggests the existence of an additional mechanism operating during lateral specification that prohibits neighboring vulval precursor cells from assuming the primary fate.},
  added-at = {2018-12-02T16:09:07.000+0100},
  address = {Department of Computer Science and Applied Mathematics, Weizmann Institute of Science, Rehovot 76100, Israel. jasmine.fixher@weizmann.ac.il},
  author = {Fisher, Jasmin and Piterman, Nir and Hubbard and Stern, Michael J. and Harel, David},
  biburl = {https://www.bibsonomy.org/bibtex/29583f1ddfcfb35ed4e94f3a005ca7024/karthikraman},
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  issn = {0027-8424},
  journal = {Proceedings of the National Academy of Sciences of the United States of America},
  keywords = {executable-biology signalling},
  month = feb,
  number = 6,
  pages = {1951--1956},
  pmid = {15684055},
  posted-at = {2009-12-17 16:01:01},
  priority = {2},
  timestamp = {2018-12-02T16:09:07.000+0100},
  title = {Computational insights into Caenorhabditis elegans vulval development},
  url = {http://dx.doi.org/10.1073/pnas.0409433102},
  volume = 102,
  year = 2005
}

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