Literature DB >> 1612585

Small eye (Sey): cloning and characterization of the murine homolog of the human aniridia gene.

C C Ton1, H Miwa, G F Saunders.   

Abstract

Phenotypic parallels and genetic evidence from comparative mapping suggest that the murine Small eye (Sey) and human aniridia (AN) disorders are homologous. This report describes the isolation of a murine embryonic cDNA that is structurally homologous to the AN cDNA were recently cloned. The murine cDNA detects a 2.7-kb transcript in the adult mouse eye and cerebellum and in human glioblastomas, suggesting a neuroectodermal involvement in the etiology of Sey/AN. Sequence comparison between the murine and the human cDNAs revealed extensive homology in nucleotide sequence (greater than 92%) and virtual identity at the amino acid level. None of the differing amino acids was located within the paired box and homeobox DNA-binding domains. These results provide evidence for a common molecular basis underlying the two genetic disorders and suggest that the Sey system would be an authentic model for human AN.

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Year:  1992        PMID: 1612585     DOI: 10.1016/0888-7543(92)90239-o

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  16 in total

1.  Dach1 mutant mice bear no gross abnormalities in eye, limb, and brain development and exhibit postnatal lethality.

Authors:  R J Davis; W Shen; Y I Sandler; M Amoui; P Purcell; R Maas; C N Ou; H Vogel; A L Beaudet; G Mardon
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

2.  Morphometric study of the optic nerve of adult normal mice and mice heterozygous for the Small eye mutation (Sey/+).

Authors:  Y Y Dangata; G S Findlater; B Dhillon; M H Kaufman
Journal:  J Anat       Date:  1994-12       Impact factor: 2.610

3.  Craniofacial abnormalities in homozygous Small eye (Sey/Sey) embryos and newborn mice.

Authors:  M H Kaufman; H H Chang; J P Shaw
Journal:  J Anat       Date:  1995-06       Impact factor: 2.610

4.  Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus.

Authors:  W Schmahl; M Knoedlseder; J Favor; D Davidson
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

Review 5.  Corneal epithelial stem cells: deficiency and regulation.

Authors:  Genevieve A Secker; Julie T Daniels
Journal:  Stem Cell Rev       Date:  2008-07-12       Impact factor: 5.739

6.  Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.

Authors:  M Drechsler; E J Meijers-Heijboer; S Schneider; B Schurich; C Grond-Ginsbach; G Tariverdian; G Kantner; A Blankenagel; D Kaps; T Schroeder-Kurth
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

7.  Tumor suppressor PAX6 functions as androgen receptor co-repressor to inhibit prostate cancer growth.

Authors:  Chih-Rong Shyr; Meng-Yin Tsai; Shuyuan Yeh; Hong-Yo Kang; Yun-Chao Chang; Pei-Ling Wong; Chao-Cheng Huang; Ko-En Huang; Chawnshang Chang
Journal:  Prostate       Date:  2010-02-01       Impact factor: 4.104

8.  Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins.

Authors:  A Martha; R E Ferrell; H Mintz-Hittner; L A Lyons; G F Saunders
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

9.  The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3.

Authors:  W J Fredericks; N Galili; S Mukhopadhyay; G Rovera; J Bennicelli; F G Barr; F J Rauscher
Journal:  Mol Cell Biol       Date:  1995-03       Impact factor: 4.272

10.  Morphometric analysis of the lens in human aniridia and mouse Small eye.

Authors:  Anna Voskresenskaya; Nadezhda Pozdeyeva; Yevgeniy Batkov; Tatyana Vasilyeva; Andrey Marakhonov; Richard A West; Jeffrey L Caplan; Ales Cvekl; Yan Wang; Melinda K Duncan
Journal:  Exp Eye Res       Date:  2020-11-26       Impact factor: 3.467

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