Effect of external retinoic acid on Tbx1 gene during zebrafish embryogenesis

OBJECTIVE: DiGeorge/del22q11 syndrome is one of the most common genetic causes of outflow tract and aortic arch defects in human. DiGeorge/del22q11 is thought to involve an embryonic defect restricted to the pharyngeal arches and the corresponding pharyngeal pouches. Previous studies have evidenced...

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Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 45(2007), 4 vom: 20. Apr., Seite 267-71
1. Verfasser: Zhang, Li-Feng (VerfasserIn)
Weitere Verfasser: Gui, Yong-Hao, Zhong, Tao, Wang, Yue-Xiang, Qian, Lin-Xi, Dong, Yong-Xin, Jiang, Qiu, Sun, Shu-Na, Song, Hou-Yan
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:Journal Article T-Box Domain Proteins Zebrafish Proteins tbr1b protein, zebrafish Tretinoin 5688UTC01R
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245 1 0 |a Effect of external retinoic acid on Tbx1 gene during zebrafish embryogenesis 
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520 |a OBJECTIVE: DiGeorge/del22q11 syndrome is one of the most common genetic causes of outflow tract and aortic arch defects in human. DiGeorge/del22q11 is thought to involve an embryonic defect restricted to the pharyngeal arches and the corresponding pharyngeal pouches. Previous studies have evidenced that retinoic acid (RA) signaling is definitely indispensable for the development of the pharyngeal arches. Tbx1, one of the T-box containing genes, is proved to be the most attractive candidate gene for DiGeorge/del22q11 syndrome. However, the interaction between RA and Tbx1 has not been fully investigated. Exploring the interaction will contribute to discover the molecular pathways disrupted in DiGeorge/del22q11 syndrome, and will also be essential for understanding genetic basis for congenital heart disease. It now seems possible that genes and molecular pathways disrupted in DiGeorge syndrome will also account for some isolated cases of congenital heart disease. Accordingly, the present study aimed to extensively study the effects of external RA on the cardiac development and Tbx1 expression during zebrafish embryogenesis 
520 |a METHODS: The chemical genetics approach was applied by treating zebrafish embryos with 5 x 10(-8) mol/L RA and 10(-7) mol/L RA at 12.5 hour post fertilization (hpf). The expression patterns of Tbx1 were monitored by whole-mount in situ hybridization and quantitative real-time RT-PCR, respectively 
520 |a RESULTS: The zebrafish embryos treated with 5 x 10(-8) mol/L RA and 10(-7) mol/L RA for 1.5 h at 12.5 hpf exhibited selective defects of abnormal heart tube. The results of whole-mount in situ hybridization with Tbx1 RNA probe showed that Tbx1 was expressed in cardiac region, pharyngeal arches and otic vesicle during zebrafish embryogenesis. RA treatment led to a distinct spatio-temporal expression pattern for Tbx1 from that in wild type embryo. The real-time PCR analysis showed that Tbx1 expression levels were markedly reduced by RA treatment. Tbx1 expression in the pharyngeal arches and heart were obviously down regulated compared to the wild type embryos. In contrast to 5 x 10(-8) mol/L RA-treated groups, 10(-7) mol/L RA caused a more severe effect on the Tbx1 expression level 
520 |a CONCLUSION: These results suggested that there was a genetic link between RA and Tbx1 during development of zebrafish embryo. RA could produce an altered Tbx1 expression pattern in zebrafish. RA may regulate the Tbx1 expression in a dose-dependant manner. RA could represent a major epigenetic factor to cause abnormal expression of Tbx1, secondarily, disrupt the pharyngeal arch and heart development 
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700 1 |a Gui, Yong-Hao  |e verfasserin  |4 aut 
700 1 |a Zhong, Tao  |e verfasserin  |4 aut 
700 1 |a Wang, Yue-Xiang  |e verfasserin  |4 aut 
700 1 |a Qian, Lin-Xi  |e verfasserin  |4 aut 
700 1 |a Dong, Yong-Xin  |e verfasserin  |4 aut 
700 1 |a Jiang, Qiu  |e verfasserin  |4 aut 
700 1 |a Sun, Shu-Na  |e verfasserin  |4 aut 
700 1 |a Song, Hou-Yan  |e verfasserin  |4 aut 
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