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Anterior Hox Genes in Cardiac Development and Great Artery Patterning

机译:心脏发育和大动脉模式中的前Hox基因

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During early development, the heart tube grows by progressive addition of progenitor cells to the arterial and venous poles. These cardiac progenitor cells, originally identified in 2001, are located in the splanchnic mesoderm in a region termed the second heart field (SHF). Since its discovery, our view of heart development has been refined and it is well established that perturbation in the addition of SHF cells results in a spectrum of congenital heart defects. We have previously shown that anterior Hox genes, including Hoxb1, Hoxa1 and Hoxa3, are expressed in distinct subdomains of the SHF that contribute to atrial and subpulmonary myocardium. It is well known that Hox proteins exert their function through interaction with members of the TALE family, including Pbx and Meis factors. The expression profile of Pbx and Meis factors overlaps with that of anterior Hox factors in the embryonic heart, and recent data suggest that they may interact together during cardiac development. This review aims to bring together recent findings in vertebrates that strongly suggest an important function for Hox, Pbx and Meis factors in heart development and disease.
机译:在早期发育期间,通过向血管和静脉极逐渐添加祖细胞来使心管生长。这些心脏祖细胞最初于2001年被鉴定,位于内脏中胚层的第二心脏区域(SHF)中。自发现以来,我们对心脏发育的观点得到了完善,并且众所周知,添加SHF细胞会引起摄动,从而导致一系列先天性心脏缺陷。我们以前已经表明,包括Hoxb1,Hoxa1和Hoxa3在内的前Hox基因在SHF的不同亚域中表达,这些亚域有助于心房和肺下心肌。众所周知,Hox蛋白通过与TALE家族成员(包括Pbx和Meis因子)相互作用而发挥其功能。在胚胎心脏中,Pbx和Meis因子的表达谱与前Hox因子的表达谱重叠,最近的数据表明它们可能在心脏发育过程中相互作用。这篇综述旨在汇集脊椎动物的最新发现,这些发现强烈暗示了Hox,Pbx和Meis因子在心脏发育和疾病中的重要作用。

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