Literature DB >> 8074321

Specification and segmentation of the paraxial mesoderm.

P P Tam1, P A Trainor.   

Abstract

Somite formation in the mouse embryo begins with the recruitment of mesenchymal cells into the paraxial mesoderm. Cells destined for the paraxial mesoderm are recruited from a progenitor population found first in the embryonic ectoderm and later in the primitive streak and the tail bud. Experimental evidence suggests that the allocation of precursor cells to different mesodermal lineages may be related to the site at which the cells ingress through the primitive streak. An increasing number of genes, such as those encoding growth factor and transcription factors, are now known to be expressed in the primitive streak. It is not known whether the specification of mesodermal cell fate has any relationship with the activity of genes that are expressed in the restricted cell populations of the primitive streak. Somitomeres, which are spherical clusters of mesenchymal cells in the presomitic mesoderm, presage the segmentation of somites in the paraxial mesoderm. The somitomeric organization denotes a pre-pattern of segmentation that defines the physical boundary and the bilateral symmetry of the mesodermal segments in the body axis. The establishment of new somitomeres seems to require the interaction of a resident cell population in the presomitic mesoderm and the incoming primitive streak cells. Cell mixing, which occurs in the somitomeres prior to somite segmentation, poses problems in understanding the developmental role of the somitomere and the real significance of the partitioning of the node-derived and primitive streak-derived cells in the mesodermal segments. In the presomitic mesoderm, the expression of some genes that encode transcription factors, growth factors or tyrosine kinase receptor, and the localization of certain cell adhesion molecules are closely associated with distinct morphogenetic events, such as cell clustering in the presomitic mesoderm and the formation of epithelial somites. There is, however, very little direct relationship between the spatial pattern of gene expression and the somitomeric organization in the presomitic mesoderm. Results of somite transplantation experiments suggest that both the segmental address and the morphogenetic characteristics of the somite may be determined during somite segmentation. Regional identity of the paraxial mesodermal segment is conferred by the expression of a combination of Hox genes in the sclerotome and probably other lineage-specific genes that are subject to imprinting. Superimposed on the global metameric pattern, two orthogonal polarities of cell differentiation are endowed in each mesodermal segment. The rostro-caudal polarity is established prior to somite segmentation. This polarity is later manifested by the subdivision of the sclerotome and the alliance of the neural crest cells and motor axons with the rostral half-somite.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Year:  1994        PMID: 8074321     DOI: 10.1007/bf00190586

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  250 in total

1.  Enhancer trap integrations in mouse embryonic stem cells give rise to staining patterns in chimaeric embryos with a high frequency and detect endogenous genes.

Authors:  R Korn; M Schoor; H Neuhaus; U Henseling; R Soininen; J Zachgo; A Gossler
Journal:  Mech Dev       Date:  1992-11       Impact factor: 1.882

2.  Connexin 43 expression in the mouse embryo: localization of transcripts within developmentally significant domains.

Authors:  C P Ruangvoravat; C W Lo
Journal:  Dev Dyn       Date:  1992-08       Impact factor: 3.780

3.  Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos.

Authors:  W C Smith; R M Harland
Journal:  Cell       Date:  1992-09-04       Impact factor: 41.582

4.  Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene.

Authors:  H Le Mouellic; Y Lallemand; P Brûlet
Journal:  Cell       Date:  1992-04-17       Impact factor: 41.582

5.  The role of extracellular matrix in the formation of the sclerotome.

Authors:  M Solursh; M Fisher; S Meier; C T Singley
Journal:  J Embryol Exp Morphol       Date:  1979-12

6.  Connectin: a homophilic cell adhesion molecule expressed on a subset of muscles and the motoneurons that innervate them in Drosophila.

Authors:  A Nose; V B Mahajan; C S Goodman
Journal:  Cell       Date:  1992-08-21       Impact factor: 41.582

7.  Murine developmental control genes.

Authors:  M Kessel; P Gruss
Journal:  Science       Date:  1990-07-27       Impact factor: 47.728

8.  Mouse homeobox gene transcripts occupy different but overlapping domains in embryonic germ layers and organs: a comparison of Hox-3.1 and Hox-1.5.

Authors:  S J Gaunt
Journal:  Development       Date:  1988-05       Impact factor: 6.868

9.  Segmental lineage restrictions in the chick embryo spinal cord depend on the adjacent somites.

Authors:  C D Stern; K F Jaques; T M Lim; S E Fraser; R J Keynes
Journal:  Development       Date:  1991-09       Impact factor: 6.868

10.  Cell proliferation in the gastrulating chick embryo: a study using BrdU incorporation and PCNA localization.

Authors:  E J Sanders; M Varedi; A S French
Journal:  Development       Date:  1993-06       Impact factor: 6.868

View more
  25 in total

Review 1.  Neural crest patterning and the evolution of the jaw.

Authors:  C B Kimmel; C T Miller; R J Keynes
Journal:  J Anat       Date:  2001 Jul-Aug       Impact factor: 2.610

2.  Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development.

Authors:  Zhen Zhang; Tuong Huynh; Antonio Baldini
Journal:  Development       Date:  2006-08-16       Impact factor: 6.868

3.  MLL, a mammalian trithorax-group gene, functions as a transcriptional maintenance factor in morphogenesis.

Authors:  B D Yu; R D Hanson; J L Hess; S E Horning; S J Korsmeyer
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

4.  T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification.

Authors:  T P Yamaguchi; S Takada; Y Yoshikawa; N Wu; A P McMahon
Journal:  Genes Dev       Date:  1999-12-15       Impact factor: 11.361

5.  Role of osteoclasts in oral homeostasis and jawbone diseases.

Authors:  Maiko Omi; Yuji Mishina
Journal:  Oral Sci Int       Date:  2020-07-21

6.  Tgfbr2 regulates the maintenance of boundaries in the axial skeleton.

Authors:  Michael O Baffi; Molly A Moran; Rosa Serra
Journal:  Dev Biol       Date:  2006-06-07       Impact factor: 3.582

7.  Homozygous inactivating mutations in the NKX3-2 gene result in spondylo-megaepiphyseal-metaphyseal dysplasia.

Authors:  Jan Hellemans; Marleen Simon; Annelies Dheedene; Yasemin Alanay; Ercan Mihci; Laila Rifai; Abdelaziz Sefiani; Yolande van Bever; Morteza Meradji; Andrea Superti-Furga; Geert Mortier
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

8.  The chick somitogenesis oscillator is arrested before all paraxial mesoderm is segmented into somites.

Authors:  Gennady Tenin; David Wright; Zoltan Ferjentsik; Robert Bone; Michael J McGrew; Miguel Maroto
Journal:  BMC Dev Biol       Date:  2010-02-25       Impact factor: 1.978

9.  Head segmentation in vertebrates.

Authors:  Shigeru Kuratani; Thomas Schilling
Journal:  Integr Comp Biol       Date:  2008-10-25       Impact factor: 3.326

10.  Differential axial requirements for lunatic fringe and Hes7 transcription during mouse somitogenesis.

Authors:  Michael Stauber; Chetana Sachidanandan; Christina Morgenstern; David Ish-Horowicz
Journal:  PLoS One       Date:  2009-11-24       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.