Literature DB >> 10965108

Molecular cloning, chromosomal localization, and expression of the murine SALL1 ortholog Sall1.

A Buck1, L Archangelo, C Dixkens, J Kohlhase.   

Abstract

SALL1 has been identified as one of now three human homologs of the region specific homeotic gene spalt (sal) of Drosophila, which encodes a zinc finger protein of characteristic structure. Mutations of SALL1 on chromosome 16q12.1 cause Townes-Brocks syndrome (TBS, OMIM no. 107480). In order to facilitate functional studies of this gene in a model organism, we searched for the murine homolog of SALL1. Here we report the genomic cloning, chromosome mapping, and partial expression analysis of the gene Sall1. Sequence comparison, Northern blot hybridization as well as the conserved chromosome location on the homologous mouse chromosome indicate that we have indeed isolated the murine homolog of SALL1. Copyright 2000 S. Karger AG, Basel.

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Year:  2000        PMID: 10965108     DOI: 10.1159/000015598

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  12 in total

1.  Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy.

Authors:  J Kohlhase; L Schubert; M Liebers; A Rauch; K Becker; S N Mohammed; R Newbury-Ecob; W Reardon
Journal:  J Med Genet       Date:  2003-07       Impact factor: 6.318

2.  Oligosyndactylism mice have an inversion of chromosome 8.

Authors:  Thomas L Wise; Dimitrina D Pravtcheva
Journal:  Genetics       Date:  2004-12       Impact factor: 4.562

3.  Sall3 is required for the terminal maturation of olfactory glomerular interneurons.

Authors:  Susan J Harrison; Mark Parrish; A Paula Monaghan
Journal:  J Comp Neurol       Date:  2008-04-10       Impact factor: 3.215

4.  Zinc finger protein sall2 is not essential for embryonic and kidney development.

Authors:  Akira Sato; Yuko Matsumoto; Urara Koide; Yuki Kataoka; Nobuaki Yoshida; Takashi Yokota; Makoto Asashima; Ryuichi Nishinakamura
Journal:  Mol Cell Biol       Date:  2003-01       Impact factor: 4.272

5.  Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear.

Authors:  Dan Zou; Derek Silvius; Sandra Rodrigo-Blomqvist; Sven Enerbäck; Pin-Xian Xu
Journal:  Dev Biol       Date:  2006-07-07       Impact factor: 3.582

6.  Expression of three spalt (sal) gene homologues in zebrafish embryos.

Authors:  Esther Camp; Rory Hope; R Daniel Kortschak; Timothy C Cox; Michael Lardelli
Journal:  Dev Genes Evol       Date:  2002-12-10       Impact factor: 0.900

7.  Sall1, sall2, and sall4 are required for neural tube closure in mice.

Authors:  Johann Böhm; Anja Buck; Wiktor Borozdin; Ashraf U Mannan; Uta Matysiak-Scholze; Ibrahim Adham; Walter Schulz-Schaeffer; Thomas Floss; Wolfgang Wurst; Jürgen Kohlhase; Francisco Barrionuevo
Journal:  Am J Pathol       Date:  2008-09-25       Impact factor: 4.307

8.  Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality.

Authors:  M Parrish; T Ott; C Lance-Jones; G Schuetz; A Schwaeger-Nickolenko; A P Monaghan
Journal:  Mol Cell Biol       Date:  2004-08       Impact factor: 4.272

9.  Drosophila spalt/spalt-related mutants exhibit Townes-Brocks' syndrome phenotypes.

Authors:  P D Si Dong; Sokol V Todi; Daniel F Eberl; Grace Boekhoff-Falk
Journal:  Proc Natl Acad Sci U S A       Date:  2003-08-18       Impact factor: 11.205

10.  Sall1 regulates cortical neurogenesis and laminar fate specification in mice: implications for neural abnormalities in Townes-Brocks syndrome.

Authors:  Susan J Harrison; Ryuichi Nishinakamura; Kevin R Jones; A Paula Monaghan
Journal:  Dis Model Mech       Date:  2011-12-22       Impact factor: 5.758

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