Literature DB >> 11523819

The vertebrate segmentation clock.

O Pourquie1.   

Abstract

Vertebrate somitogenesis has been shown to be associated with a molecular oscillator, the segmentation clock, whose periodicity matches that of the process of somitogenesis. The existence of such a clock in presomitic mesoderm (PSM) cells was originally proposed in theoretical models such as the 'clock and wavefront'. Molecular evidence for the existence of this clock in vertebrates has been obtained on the basis of the periodic expression of several genes, most of which are related to the Notch signalling pathway. These genes are expressed in a dynamic sequence which appears as a wave sweeping caudo-rostrally along the whole PSM once during each somite formation. Notch-pathway mouse and fish mutants lose the dynamic expression of the cycling genes, indicating that Notch signalling is required for their periodic expression, or is required to coordinate the oscillations between PSM cells. Therefore Notch signalling is either part of the mechanism of the oscillator itself or acts as a cofactor required for cycling gene expression. A further potentially important role for the segmentation clock is to periodically activate Notch signalling in the rostral presomitic mesoderm, thereby generating the periodic formation of somite boundaries.

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Year:  2001        PMID: 11523819      PMCID: PMC1594994          DOI: 10.1046/j.1469-7580.2001.19910169.x

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  25 in total

Review 1.  Notch around the clock.

Authors:  O Pourquié
Journal:  Curr Opin Genet Dev       Date:  1999-10       Impact factor: 5.578

2.  Notch signalling and the synchronization of the somite segmentation clock.

Authors:  Y J Jiang; B L Aerne; L Smithers; C Haddon; D Ish-Horowicz; J Lewis
Journal:  Nature       Date:  2000-11-23       Impact factor: 49.962

3.  Fringe is a glycosyltransferase that modifies Notch.

Authors:  D J Moloney; V M Panin; S H Johnston; J Chen; L Shao; R Wilson; Y Wang; P Stanley; K D Irvine; R S Haltiwanger; T F Vogt
Journal:  Nature       Date:  2000-07-27       Impact factor: 49.962

4.  The notch signalling regulator fringe acts in the Golgi apparatus and requires the glycosyltransferase signature motif DXD.

Authors:  S Munro; M Freeman
Journal:  Curr Biol       Date:  2000-07-13       Impact factor: 10.834

5.  Control of her1 expression during zebrafish somitogenesis by a delta-dependent oscillator and an independent wave-front activity.

Authors:  S A Holley; R Geisler; C Nüsslein-Volhard
Journal:  Genes Dev       Date:  2000-07-01       Impact factor: 11.361

6.  Structure, chromosomal locus, and promoter analysis of the gene encoding the mouse helix-loop-helix factor HES-1. Negative autoregulation through the multiple N box elements.

Authors:  K Takebayashi; Y Sasai; Y Sakai; T Watanabe; S Nakanishi; R Kageyama
Journal:  J Biol Chem       Date:  1994-02-18       Impact factor: 5.157

7.  Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors.

Authors:  C Leimeister; K Dale; A Fischer; B Klamt; M Hrabe de Angelis; F Radtke; M J McGrew; O Pourquié; M Gessler
Journal:  Dev Biol       Date:  2000-11-01       Impact factor: 3.582

8.  Signalling downstream of activated mammalian Notch.

Authors:  S Jarriault; C Brou; F Logeat; E H Schroeter; R Kopan; A Israel
Journal:  Nature       Date:  1995-09-28       Impact factor: 49.962

9.  A cell lineage analysis of segmentation in the chick embryo.

Authors:  C D Stern; S E Fraser; R J Keynes; D R Primmett
Journal:  Development       Date:  1988       Impact factor: 6.868

10.  Notch signalling is required for cyclic expression of the hairy-like gene HES1 in the presomitic mesoderm.

Authors:  C Jouve; I Palmeirim; D Henrique; J Beckers; A Gossler; D Ish-Horowicz; O Pourquié
Journal:  Development       Date:  2000-04       Impact factor: 6.868

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  17 in total

1.  Sensory neuron differentiation is regulated by notch signaling in the trigeminal placode.

Authors:  Rhonda N T Lassiter; Matthew K Ball; Jason S Adams; Brian T Wright; Michael R Stark
Journal:  Dev Biol       Date:  2010-06-09       Impact factor: 3.582

2.  Mesodermal cell displacements during avian gastrulation are due to both individual cell-autonomous and convective tissue movements.

Authors:  Evan A Zamir; András Czirók; Cheng Cui; Charles D Little; Brenda J Rongish
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-18       Impact factor: 11.205

Review 3.  Why is delta endocytosis required for effective activation of notch?

Authors:  Ajay Chitnis
Journal:  Dev Dyn       Date:  2006-04       Impact factor: 3.780

Review 4.  Mathematical models for somite formation.

Authors:  Ruth E Baker; Santiago Schnell; Philip K Maini
Journal:  Curr Top Dev Biol       Date:  2008       Impact factor: 4.897

Review 5.  From segment to somite: segmentation to epithelialization analyzed within quantitative frameworks.

Authors:  Paul M Kulesa; Santiago Schnell; Stefan Rudloff; Ruth E Baker; Philip K Maini
Journal:  Dev Dyn       Date:  2007-06       Impact factor: 3.780

6.  How can mathematics help us explore vertebrate segmentation?

Authors:  Ruth E Baker; Santiago Schnell
Journal:  HFSP J       Date:  2009-01-27

7.  Positional information, positional error, and readout precision in morphogenesis: a mathematical framework.

Authors:  Gašper Tkačik; Julien O Dubuis; Mariela D Petkova; Thomas Gregor
Journal:  Genetics       Date:  2014-10-31       Impact factor: 4.562

Review 8.  Environmental aspects of congenital scoliosis.

Authors:  Zheng Li; Xin Yu; Jianxiong Shen
Journal:  Environ Sci Pollut Res Int       Date:  2015-01-29       Impact factor: 4.223

9.  Dynamic properties of the segmentation clock mediated by microRNA.

Authors:  Bo Jing; Julin Yuan; Zhongqiong Yin; Cheng Lv; Shengming Lu; Haoshan Xiong; Huaqiao Tang; Gang Ye; Fei Shi
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

10.  Mir-125a-5p-mediated regulation of Lfng is essential for the avian segmentation clock.

Authors:  Maurisa F Riley; Matthew S Bochter; Kanu Wahi; Gerard J Nuovo; Susan E Cole
Journal:  Dev Cell       Date:  2013-03-11       Impact factor: 12.270

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