Literature DB >> 1889089

The molecular basis of the undulated/Pax-1 mutation.

G Chalepakis1, R Fritsch, H Fickenscher, U Deutsch, M Goulding, P Gruss.   

Abstract

The murine paired box gene Pax-1 has been associated with the mouse developmental mutant undulated (un), which exhibits malformations in the vertebral column. In un mice, a point mutation leading to a Gly-Ser exchange in a conserved part of the paired domain of Pax-1 is present. Here we show that Pax-1 encodes a DNA-binding protein with transcriptional activating properties. The DNA-binding specificity of the Pax-1 protein has been extensively analyzed in gel shift assays, and in conjunction with binding interference experiments, a DNA-binding core motif was defined. Comparison of the DNA-binding properties of wild-type and un Pax-1 proteins demonstrates that the Gly-Ser replacement at position 15 within the paired domain dramatically decreases the DNA-binding affinity of the un Pax-1 protein and alters its DNA-binding specificity. These results decipher the molecular basis of the un mutation.

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Year:  1991        PMID: 1889089     DOI: 10.1016/0092-8674(91)90434-z

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  65 in total

1.  A novel murine homeobox gene isolated by a tissue specific PCR cloning strategy.

Authors:  M J Kern; D P Witte; M T Valerius; B J Aronow; S S Potter
Journal:  Nucleic Acids Res       Date:  1992-10-11       Impact factor: 16.971

2.  Pax-8, a paired domain-containing protein, binds to a sequence overlapping the recognition site of a homeodomain and activates transcription from two thyroid-specific promoters.

Authors:  M Zannini; H Francis-Lang; D Plachov; R Di Lauro
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

3.  AKT and PAX3-FKHR cooperation enforces myogenic differentiation blockade in alveolar rhabdomyosarcoma cell.

Authors:  Mathivanan Jothi; Kochi Nishijo; Charles Keller; Asoke K Mal
Journal:  Cell Cycle       Date:  2012-03-01       Impact factor: 4.534

4.  Comparative study of Pax2 expression in glial cells in the retina and optic nerve of birds and mammals.

Authors:  Jennifer Stanke; Holly E Moose; Heithem M El-Hodiri; Andy J Fischer
Journal:  J Comp Neurol       Date:  2010-06-15       Impact factor: 3.215

Review 5.  Current perspectives on the genetic causes of neural tube defects.

Authors:  Patrizia De Marco; Elisa Merello; Samantha Mascelli; Valeria Capra
Journal:  Neurogenetics       Date:  2006-08-29       Impact factor: 2.660

6.  Pax-1 in the development of the cervico-occipital transitional zone.

Authors:  J Wilting; C Ebensperger; T S Müller; H Koseki; J Wallin; B Christ
Journal:  Anat Embryol (Berl)       Date:  1995-09

7.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-01-11       Impact factor: 16.971

8.  A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.

Authors:  Dolrudee Jumlongras; Jenn-Yih Lin; Anas Chapra; Christine E Seidman; Jonathan G Seidman; Richard L Maas; Bjorn R Olsen
Journal:  Hum Genet       Date:  2003-12-19       Impact factor: 4.132

9.  Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos.

Authors:  C Ebensperger; J Wilting; B Brand-Saberi; Y Mizutani; B Christ; R Balling; H Koseki
Journal:  Anat Embryol (Berl)       Date:  1995-04

10.  Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins.

Authors:  P H Joosten; F A Hol; S E van Beersum; H Peters; B C Hamel; G B Afink; E J van Zoelen; E C Mariman
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

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