Literature DB >> 8026631

Early determination and permissive expression of amelogenin transcription during mouse mandibular first molar development.

R I Couwenhoven1, M L Snead.   

Abstract

The expression of tissue-specific enamel matrix genes is believed to require both instructive and permissive interactions of enamel organ epithelium with dental papilla mesenchyme and/or extracellular matrix during a restricted period of development. Biosynthesis of amelogenin gene products has been found to be associated with the terminal differentiation of inner enamel organ epithelium. The developing mouse first mandibular molar was used for a detailed examination of the temporal initiation and developmental pattern of amelogenin transcription. These studies define temporally instructive versus permissive influences on amelogenin transcription. During in vivo development, amelogenin transcripts were detected in late cap (15 days in utero; E15) through bell stage (E16 through E19) mouse molar tooth formation utilizing reverse transcription coupled to polymerase chain reaction amplification. Alternatively spliced amelogenin transcripts were detected in late bell stage (E18) molars. Amelogenin transcripts were also detected in isolated late cap stage (E15) enamel organ epithelium dissected free of dental papilla mesenchyme and cultured within a substitute basement membrane gel, but not in identical cap stage enamel organ epithelium cultured on plastic or a laminin-coated filter. Amelogenin transcripts were also found in early cap stage (E14) isolated enamel organ epithelium cultured within a basement membrane gel, but were not detected in enamel organ epithelium isolated from earlier stages of odontogenesis and cultured within a basement membrane gel. The results of these experiments indicate that a basement membrane gel is a useful extracellular substrate which provides permissive interactions required for the expression of amelogenin transcripts by enamel organ epithelium and that instructive interactions which determine enamel organ epithelium to become committed to amelogenin transcription occur prior to the early cap stage (E14) of odontogenesis. The results also suggest that continued interactions of enamel organ epithelium with dental papilla mesenchyme serve to regulate amelogenin transcription and post-transcriptional amelogenin RNA splicing in a complex manner during odontogenesis.

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Year:  1994        PMID: 8026631     DOI: 10.1006/dbio.1994.1199

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


  9 in total

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4.  Proliferation and differentiation of fetal rat pulmonary epithelium in the absence of mesenchyme.

Authors:  R R Deterding; J M Shannon
Journal:  J Clin Invest       Date:  1995-06       Impact factor: 14.808

5.  Biological synthesis of tooth enamel instructed by an artificial matrix.

Authors:  Zhan Huang; Christina J Newcomb; Pablo Bringas; Samuel I Stupp; Malcolm L Snead
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6.  Transcription factor Sp3 is essential for post-natal survival and late tooth development.

Authors:  P Bouwman; H Göllner; H P Elsässer; G Eckhoff; A Karis; F Grosveld; S Philipsen; G Suske
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7.  Alternative splicing of the mouse amelogenin primary RNA transcript.

Authors:  J P Simmer; C C Hu; E C Lau; P Sarte; H C Slavkin; A G Fincham
Journal:  Calcif Tissue Int       Date:  1994-10       Impact factor: 4.333

8.  Binding of amelogenin to MMP-9 and their co-expression in developing mouse teeth.

Authors:  Junsheng Feng; Jennifer S McDaniel; Hui-Hsiu Chuang; Ouwen Huang; Audrey Rakian; Xiaoping Xu; Bjorn Steffensen; Kevin J Donly; Mary MacDougall; Shuo Chen
Journal:  J Mol Histol       Date:  2012-05-31       Impact factor: 2.611

9.  Expression of Notch 1, 2 and 3 is regulated by epithelial-mesenchymal interactions and retinoic acid in the developing mouse tooth and associated with determination of ameloblast cell fate.

Authors:  T A Mitsiadis; M Lardelli; U Lendahl; I Thesleff
Journal:  J Cell Biol       Date:  1995-07       Impact factor: 10.539

  9 in total

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