Literature DB >> 9389448

System to identify individual somites and their derivatives in the developing mouse embryo.

R Spörle1, K Schughart.   

Abstract

The identification of the axial levels of metameric elements along the rostro-caudal axis of vertebrates until now was not possible before late, fetal development, when the vertebral anlagen first appear. We developed a new system for the exact axial identification of somites and their derivatives from early, embryonic stages of mouse development on (Theiler stages (TS) 15 to TS18-19). The initial axial identification of the somites was performed by relating them to the rostral-most two cervical spinal ganglia (SG), that exhibited characteristic morphologies (SG-C1: bar-like, SG-C2: triangular). At all stages of somitic development, the most prominent somite along the rostro-caudal axis correlated with the bar-like SG-C1, and, therefore, we named it the first cervical somite (SO-C1). The next step, the axial identification of the somites independently from the SG, was based on the observation that after in situ hybridization to Myf5, Pax3, Pax1, and Mox1 riboprobes, a distinct and characteristic morphology of the last occipital somite (SO-O5) and the first two cervical somites (SO-C1, SO-C2) can be observed. From TS15 on, these three somites formed a triad of the most prominent somites along the rostro-caudal axis. Also, the dermomyotomal, myotomal, and sclerotomal derivatives of this somite triad were the most prominent in later somitic development. Furthermore, SG-C1 and SG-C2 exhibited a transient bipartite anlagen in their early development, suggesting a "resegmentation" during SG formation. Later, when somites started to dissolve, the caudal moiety of the bar-like SG-C1 anlagen fused to the anlagen of SG-C2.

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Year:  1997        PMID: 9389448     DOI: 10.1002/(SICI)1097-0177(199711)210:3<216::AID-AJA3>3.0.CO;2-J

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  5 in total

1.  The initial somitic phase of Myf5 expression requires neither Shh signaling nor Gli regulation.

Authors:  Lydia Teboul; Dennis Summerbell; Peter W J Rigby
Journal:  Genes Dev       Date:  2003-12-01       Impact factor: 11.361

2.  Developmental origin and morphogenesis of the diaphragm, an essential mammalian muscle.

Authors:  Elizabeth M Sefton; Mirialys Gallardo; Gabrielle Kardon
Journal:  Dev Biol       Date:  2018-04-19       Impact factor: 3.582

3.  Closure of the vertebral canal in human embryos and fetuses.

Authors:  Hayelom K Mekonen; Jill P J M Hikspoors; Greet Mommen; Nutmethee Kruepunga; S Eleonore Köhler; Wouter H Lamers
Journal:  J Anat       Date:  2017-06-05       Impact factor: 2.610

4.  Fgf4 maintains Hes7 levels critical for normal somite segmentation clock function.

Authors:  Matthew J Anderson; Valentin Magidson; Ryoichiro Kageyama; Mark Lewandoski
Journal:  Elife       Date:  2020-11-19       Impact factor: 8.140

5.  Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton.

Authors:  Susan Skuntz; Baljinder Mankoo; Minh-Thanh T Nguyen; Elisabeth Hustert; Atsuo Nakayama; Elisabeth Tournier-Lasserve; Christopher V E Wright; Vassilis Pachnis; Kapil Bharti; Heinz Arnheiter
Journal:  Dev Biol       Date:  2009-06-09       Impact factor: 3.582

  5 in total

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