jumonji gene is essential for the neurulation and cardiac development of mouse embryos with a C3H/He background

The recessive mutant mouse jumonji ( jmj), obtained by a gene trap strategy, shows neural tube defects in approximately half of homozygous embryos with a BALB/cA and 129/Ola mixed background, but no neural tube defects with BALB/cA, C57BL/6J, and DBA/2J backgrounds. Here, we show that neural tube an...

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Published in:Mechanisms of development Vol. 86; no. 1; pp. 29 - 38
Main Authors: Takeuchi, Takashi, Kojima, Mizuyo, Nakajima, Kuniko, Kondo, Shunzo
Format: Journal Article
Language:English
Published: Ireland Elsevier Ireland Ltd 01-08-1999
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Abstract The recessive mutant mouse jumonji ( jmj), obtained by a gene trap strategy, shows neural tube defects in approximately half of homozygous embryos with a BALB/cA and 129/Ola mixed background, but no neural tube defects with BALB/cA, C57BL/6J, and DBA/2J backgrounds. Here, we show that neural tube and cardiac defects are observed in all embryos with a C3H/HeJ background. In addition, abnormal groove formation and prominent flexure are observed on the neural plate with full penetrance, suggesting that abnormal groove formation leads to neural tube defects. We found morphogenetic abnormalities in the bulbus cordis (future outflow tract and the right ventricle) of homozygous embryo hearts. Moreover, myocytes in the ventricular trabeculae show hyperplasia with cells filling the ventricles. Together with the observation that the jmj gene is expressed in the neural epithelium of the head neural plate and in myocytes in the bulbus cordis and trabeculae, the results show that the jmj gene plays essential roles in the normal development of the neural plate, morphogenesis of bulbus cordis, and proliferation of trabecular myocytes on a C3H/He background.
AbstractList The recessive mutant mouse jumonji (jmj), obtained by a gene trap strategy, shows neural tube defects in approximately half of homozygous embryos with a BALB/cA and 129/Ola mixed background, but no neural tube defects with BALB/cA, C57BL/6J, and DBA/2J backgrounds. Here, we show that neural tube and cardiac defects are observed in all embryos with a C3H/HeJ background. In addition, abnormal groove formation and prominent flexure are observed on the neural plate with full penetrance, suggesting that abnormal groove formation leads to neural tube defects. We found morphogenetic abnormalities in the bulbus cordis (future outflow tract and the right ventricle) of homozygous embryo hearts. Moreover, myocytes in the ventricular trabeculae show hyperplasia with cells filling the ventricles. Together with the observation that the jmj gene is expressed in the neural epithelium of the head neural plate and in myocytes in the bulbus cordis and trabeculae, the results show that the jmj gene plays essential roles in the normal development of the neural plate, morphogenesis of bulbus cordis, and proliferation of trabecular myocytes on a C3H/He background.
The recessive mutant mouse jumonji ( jmj), obtained by a gene trap strategy, shows neural tube defects in approximately half of homozygous embryos with a BALB/cA and 129/Ola mixed background, but no neural tube defects with BALB/cA, C57BL/6J, and DBA/2J backgrounds. Here, we show that neural tube and cardiac defects are observed in all embryos with a C3H/HeJ background. In addition, abnormal groove formation and prominent flexure are observed on the neural plate with full penetrance, suggesting that abnormal groove formation leads to neural tube defects. We found morphogenetic abnormalities in the bulbus cordis (future outflow tract and the right ventricle) of homozygous embryo hearts. Moreover, myocytes in the ventricular trabeculae show hyperplasia with cells filling the ventricles. Together with the observation that the jmj gene is expressed in the neural epithelium of the head neural plate and in myocytes in the bulbus cordis and trabeculae, the results show that the jmj gene plays essential roles in the normal development of the neural plate, morphogenesis of bulbus cordis, and proliferation of trabecular myocytes on a C3H/He background.
Author Kojima, Mizuyo
Kondo, Shunzo
Nakajima, Kuniko
Takeuchi, Takashi
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  surname: Kondo
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/10446263$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords Cell proliferation
Ventricular trabeculae
Heart morphogenesis
Neural tube defects
Bulbus cordis
Gene trap
Neural plate
Cardiac defects
Neurulation
Cardiac myocytes
Myogenesis
jumonji
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Snippet The recessive mutant mouse jumonji ( jmj), obtained by a gene trap strategy, shows neural tube defects in approximately half of homozygous embryos with a...
The recessive mutant mouse jumonji (jmj), obtained by a gene trap strategy, shows neural tube defects in approximately half of homozygous embryos with a...
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SubjectTerms Animals
Bulbus cordis
Cardiac defects
Cardiac myocytes
Cell proliferation
Disease Models, Animal
Gene Expression Regulation, Developmental
Gene trap
Heart - embryology
Heart Defects, Congenital - genetics
Heart Defects, Congenital - pathology
Heart Defects, Congenital - veterinary
Heart morphogenesis
Heart Ventricles - metabolism
Homozygote
jumonji
Mice
Mice, Inbred BALB C
Mice, Inbred C3H - genetics
Mice, Mutant Strains
Myocardium - cytology
Myocardium - pathology
Myogenesis
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - metabolism
Neural plate
Neural tube defects
Neural Tube Defects - genetics
Neural Tube Defects - veterinary
Neurulation
Phenotype
Polycomb Repressive Complex 2
Rodent Diseases - genetics
Ventricular trabeculae
Title jumonji gene is essential for the neurulation and cardiac development of mouse embryos with a C3H/He background
URI https://dx.doi.org/10.1016/S0925-4773(99)00100-8
https://www.ncbi.nlm.nih.gov/pubmed/10446263
https://search.proquest.com/docview/69958099
Volume 86
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