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Favor, J. ; Bradley, A.* ; Conte, N.* ; Janik, D.* ; Pretsch, W. ; Reitmeir, P. ; Rosemann, M. ; Schmahl, W.* ; Wienberg, J.* ; Zaus, I.

Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes.

Genetics 182, 1077-1088 (2009)
Open Access Green as soon as Postprint is submitted to ZB.
In the mouse pax6 function is critical in a dose-dependent manner for proper eye development. pax6 Configuous gene deletions were shown to be homozygous lethal at an early embryonic stage. Heterozygotes express belly spotting and extreme microphthalmia. The eye phenotype is more Severe than in heterozygous pax6, intragenic null mutants, raising the possibility that deletions are functionally different. from intragenic null mutations or that a region distinct from Pax6 included in the deletions affects eye phenotype. we recovered and identified the exact regions deleted in three new Pax6 deletions. All are homozygous lethal at an early embryonic stage. None express belly spotting. One expresses extreme microphthalmia and two express the milder eye phenotype similar to Pax6 intragenic null mutants. Analysis of Pax6 expression levels and the major isoforms excluded the hypothesis that the deletions expressing extreme microphthalmia are directly due to the action of pax6 and functionally different from intragenic null mutations. A region distinct from Pax6 containing eight genes was identified for bell), spotting. A second region containing one gene (Rcn I) was identified for the extreme microphthalmia phenotype. Rcn1 is a Ca+2 -binding protein, resident in the endoplasmic reticulum, participates in the secretory pathway and expressed in the eye. Our results suggest that deletion of Rcn1 directly or indirectly contributes to the eye phenotype in Pax6 contiguous gene deletions.
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Publication type Article: Journal article
Document type Scientific Article
Keywords ef-hand motifs; resident CA2+-binding protein; wilms tumor association; 11P interstitial deletion; multiple exostoses ext2; endoplasmic-reticulum; mental-retardation; parietal foramina; wagr locus; molecular analysis
ISSN (print) / ISBN 0016-6731
e-ISSN 0016-6731
Journal Genetics
Quellenangaben Volume: 182, Issue: 4, Pages: 1077-1088 Article Number: , Supplement: ,
Publisher Genetics Society of America
Publishing Place Baltimore
Reviewing status Peer reviewed