%0 Journal Article %1 Gessler.2002 %A Gessler, M. %A Knobeloch, K. P. %A Helisch, A. %A Amann, K. %A Schumacher, N. %A Rohde, E. %A Fischer, A. %A Leimeister, C. %D 2002 %J Curr Biol %K *Mutation *Zebrafish Animals Aortic Basic Cardiomyopathy;Hypertrophic;Familial/embryology/*genetics/pathology Coarctation/*genetics Evolution Expression Factors Factors/*deficiency/*genetics/physiology Gene Helix-Loop-Helix Humans Hybridization In Mice Mice;Knockout Phenotype Proteins Proteins/*genetics Situ Transcription Zebrafish/genetics %N 18 %P 1601--1604 %T Mouse gridlock: no aortic coarctation or deficiency, but fatal cardiac defects in Hey2 -/- mice %V 12 %X Gridlock (grl) is one of the first mutations characterized from the large zebrafish mutagenesis screens, and it results in an arterial (aortic) maturation defect, which was proposed to resemble aortic coarctation, a clinically important human malformation. While the grl mutation appears to be a hypomorph, grl knockdown experiments have shown even stronger effects on arterial development. We have generated a knockout of the murine Hey2 (gridlock) gene to analyze the mammalian phenotype. Surprisingly, Hey2 loss does not affect aortic development, but it instead leads to a massive postnatal cardiac hypertrophy with high lethality during the first 10 days of life. This cardiomyopathy is ameliorated with time in surviving animals that do not appear to be manifestly impaired during adult life. These differences in phenotypes suggest that changes in expression or function of genes during evolution may lead to quite different pathological phenotypes, if impaired.

@article{Gessler.2002, abstract = {Gridlock (grl) is one of the first mutations characterized from the large zebrafish mutagenesis screens, and it results in an arterial (aortic) maturation defect, which was proposed to resemble aortic coarctation, a clinically important human malformation. While the grl mutation appears to be a hypomorph, grl knockdown experiments have shown even stronger effects on arterial development. We have generated a knockout of the murine Hey2 (gridlock) gene to analyze the mammalian phenotype. Surprisingly, Hey2 loss does not affect aortic development, but it instead leads to a massive postnatal cardiac hypertrophy with high lethality during the first 10 days of life. This cardiomyopathy is ameliorated with time in surviving animals that do not appear to be manifestly impaired during adult life. These differences in phenotypes suggest that changes in expression or function of genes during evolution may lead to quite different pathological phenotypes, if impaired.}, added-at = {2013-01-29T13:47:26.000+0100}, author = {Gessler, M. and Knobeloch, K. P. and Helisch, A. and Amann, K. and Schumacher, N. and Rohde, E. and Fischer, A. and Leimeister, C.}, biburl = {https://www.bibsonomy.org/bibtex/2a6e73cc02b99e20bd6ef69896c59a778/ebch}, interhash = {0cb011fd51cc62c908ad56a95255e45f}, intrahash = {a6e73cc02b99e20bd6ef69896c59a778}, journal = {Curr Biol}, keywords = {*Mutation *Zebrafish Animals Aortic Basic Cardiomyopathy;Hypertrophic;Familial/embryology/*genetics/pathology Coarctation/*genetics Evolution Expression Factors Factors/*deficiency/*genetics/physiology Gene Helix-Loop-Helix Humans Hybridization In Mice Mice;Knockout Phenotype Proteins Proteins/*genetics Situ Transcription Zebrafish/genetics}, number = 18, pages = {1601--1604}, timestamp = {2013-01-29T13:47:43.000+0100}, title = {Mouse gridlock: no aortic coarctation or deficiency, but fatal cardiac defects in Hey2 -/- mice}, volume = 12, year = 2002 }