Literature DB >> 8005030

Normal neurulation in mammals.

G Morriss-Kay1, H Wood, W H Chen.   

Abstract

During mammalian neurulation regional differences are evident between the cranial region, in which neurulation is most complex, the trunk as far as the caudal neuropore and the secondary neurulation region of the caudal trunk plus tail. Differences among these three regions are characterized by specific patterns of morphogenesis and by specific patterns of gene expression. During cranial neurulation distinct regions develop in the brain and the presomitic hindbrain forms seven rhombomeric divisions. The first clear morphological boundary is the preotic sulcus (later transformed into the gyrus between rhombomeres 2 and 3), which may limit cell movement as neuroepithelial cells rostral to it flow towards and into the rapidly expanding forebrain region. The formation of rhombomeres as morphological entities and the development of a normal rhombomere-specific pattern of homeobox and other gene expression domains depend on relatively low levels of retinoic acid. Retinoic acid receptors, which are retinoic acid-activated transcription factors, and retinoid binding proteins, which control the availability of retinoic acid to the receptors, show regional patterns of expression in the cranial, trunk and caudal regions of the neuroepithelium during neurulation. These patterns suggest a possible mechanism for region-specific gene expression during neurulation.

Entities:  

Mesh:

Year:  1994        PMID: 8005030     DOI: 10.1002/9780470514559.ch4

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  6 in total

1.  Mitotic activity and rosette formation in the neuroepithelium of the human embryo neocortex in vitro.

Authors:  E B Smirnov; I P Bystròn; V F Puchkov; V A Otellin
Journal:  Neurosci Behav Physiol       Date:  1998 Sep-Oct

2.  Dynamic imaging and quantitative analysis of cranial neural tube closure in the mouse embryo using optical coherence tomography.

Authors:  Shang Wang; Monica D Garcia; Andrew L Lopez; Paul A Overbeek; Kirill V Larin; Irina V Larina
Journal:  Biomed Opt Express       Date:  2016-12-21       Impact factor: 3.732

3.  Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development.

Authors:  M Berk; S Y Desai; H C Heyman; C Colmenares
Journal:  Genes Dev       Date:  1997-08-15       Impact factor: 11.361

Review 4.  The mechanical forces that shape our senses.

Authors:  Anh Phuong Le; Jin Kim; Karl R Koehler
Journal:  Development       Date:  2022-03-31       Impact factor: 6.862

5.  A novel genetic mechanism regulates dorsolateral hinge-point formation during zebrafish cranial neurulation.

Authors:  Molly K Nyholm; Salim Abdelilah-Seyfried; Yevgenya Grinblat
Journal:  J Cell Sci       Date:  2009-05-26       Impact factor: 5.285

6.  Microtubule-associated protein 1b is required for shaping the neural tube.

Authors:  Pradeepa Jayachandran; Valerie N Olmo; Stephanie P Sanchez; Rebecca J McFarland; Eudorah Vital; Jonathan M Werner; Elim Hong; Neus Sanchez-Alberola; Aleksey Molodstov; Rachel M Brewster
Journal:  Neural Dev       Date:  2016-01-18       Impact factor: 3.842

  6 in total

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