Literature DB >> 16545363

her1 and her13.2 are jointly required for somitic border specification along the entire axis of the fish embryo.

Dirk Sieger1, Bastian Ackermann, Christoph Winkler, Diethard Tautz, Martin Gajewski.   

Abstract

Delta-Notch and FGF signaling are involved in the control of somitogenesis in zebrafish. her genes are generally known as downstream targets of Delta-Notch signaling, but the her13.2 gene from zebrafish has recently been shown to depend on FGF signaling only. We have here studied the functional role of her13.2 in conjunction with her genes that are under Delta-Notch control. We show that joint inactivation of her1 and her13.2 leads to a complete loss of all somitic borders, including the most anterior ones. This somitic phenotype is much stronger than would be expected from the effects of the inactivation of either gene alone. A joint inactivation of her13.2 and her7, which is a paralogue of her1, does not show this enhanced effect. Thus, our results confirm inferences from in vitro studies that her1 and her13.2 form specific heterodimers, which may directly be required for regulating further target genes. These two her genes thus constitute the link between Delta-Notch pathway and FGF signaling during entire somitogenesis. We show that this interaction is conserved in the rice fish medaka, as a joint inactivation of the respective orthologues leads also to the same phenotype as in zebrafish. In addition, our results suggest that the mechanisms for anterior and posterior somite formation are not principally different, although the anterior somites often seem more refractory to genetic perturbations.

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Year:  2006        PMID: 16545363     DOI: 10.1016/j.ydbio.2006.02.003

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  8 in total

1.  The Her7 node modulates the network topology of the zebrafish segmentation clock via sequestration of the Hes6 hub.

Authors:  Anna Trofka; Jamie Schwendinger-Schreck; Tim Brend; William Pontius; Thierry Emonet; Scott A Holley
Journal:  Development       Date:  2012-01-25       Impact factor: 6.868

2.  The kinetics in mathematical models on segmentation clock genes in zebrafish.

Authors:  Kuan-Wei Chen; Kang-Ling Liao; Chih-Wen Shih
Journal:  J Math Biol       Date:  2017-05-25       Impact factor: 2.259

3.  Somitogenesis clock-wave initiation requires differential decay and multiple binding sites for clock protein.

Authors:  Mark Campanelli; Tomás Gedeon
Journal:  PLoS Comput Biol       Date:  2010-04-01       Impact factor: 4.475

4.  Intrinsic noise, Delta-Notch signalling and delayed reactions promote sustained, coherent, synchronized oscillations in the presomitic mesoderm.

Authors:  Joseph W Baron; Tobias Galla
Journal:  J R Soc Interface       Date:  2019-11-27       Impact factor: 4.118

5.  Single-cell-resolution imaging of the impact of Notch signaling and mitosis on segmentation clock dynamics.

Authors:  Emilie A Delaune; Paul François; Nathan P Shih; Sharon L Amacher
Journal:  Dev Cell       Date:  2012-11-13       Impact factor: 12.270

6.  Modeling the zebrafish segmentation clock's gene regulatory network constrained by expression data suggests evolutionary transitions between oscillating and nonoscillating transcription.

Authors:  Jamie Schwendinger-Schreck; Yuan Kang; Scott A Holley
Journal:  Genetics       Date:  2014-03-24       Impact factor: 4.562

7.  Topology and dynamics of the zebrafish segmentation clock core circuit.

Authors:  Christian Schröter; Saúl Ares; Luis G Morelli; Alina Isakova; Korneel Hens; Daniele Soroldoni; Martin Gajewski; Frank Jülicher; Sebastian J Maerkl; Bart Deplancke; Andrew C Oates
Journal:  PLoS Biol       Date:  2012-07-24       Impact factor: 8.029

8.  Small molecule screen in embryonic zebrafish using modular variations to target segmentation.

Authors:  Sandra Richter; Ulrike Schulze; Pavel Tomançak; Andrew C Oates
Journal:  Nat Commun       Date:  2017-12-01       Impact factor: 14.919

  8 in total

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