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The ascidian Mesp gene specifies heart precursor cells.

机译:海鞘Mesp基因指定心脏前体细胞。

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Understanding the molecular basis of heart development is an important research area, because malformation of the cardiovascular system is among the most frequent inborn defects. Although recent research has identified molecules responsible for heart morphogenesis in vertebrates, the initial specification of heart progenitors has not been well characterized. Ascidians provide an appropriate experimental system for exploring this specification mechanism, because the lineage for the juvenile heart is well characterized, with B7.5 cells at the 110-cell stage giving rise to embryonic trunk ventral cells (TVCs) or the juvenile heart progenitors. Here, we show that Cs-Mesp, the sole ortholog of vertebrate Mesp genes in the ascidian Ciona savignyi, is specifically and transiently expressed in the embryonic heart progenitor cells (B7.5 cells). Cs-Mesp is essential for the specification of heart precursor cells, in which Nkx, HAND and HAND-like (NoTrlc) genes are expressed. As a result, knockdown of Cs-Mesp with specific morpholino antisense oligonucleotides causes failure of the development of the juvenile heart. Together with previous evidence obtained in mice, the present results suggest that a mechanism for heart specification beginning with Mesp through Nkx and HAND is conserved among chordates.
机译:了解心脏发育的分子基础是重要的研究领域,因为心血管系统畸形是最常见的先天性缺陷之一。尽管最近的研究已经确定了脊椎动物中负责心脏形态发生的分子,但是心脏祖细胞的初始规格尚未得到很好的表征。海鞘提供了一个探索该特定机制的合适实验系统,因为对少年心脏的谱系具有很好的特征,在110细胞阶段的B7.5细胞会产生胚胎躯干腹侧细胞(TVC)或少年心脏祖细胞。在这里,我们显示Cs-Mesp是海鞘Ciona savignyi中脊椎动物Mesp基因的唯一直系同源基因,在胚胎心脏祖细胞(B7.5细胞)中特异性且瞬时表达。 Cs-Mesp对于心脏前体细胞的规范至关重要,在心脏前体细胞中表达Nkx,HAND和类似HAND的基因(NoTrlc)。结果,用特定的吗啉代反义寡核苷酸敲低Cs-Mesp导致少年心脏发育失败。与在小鼠中获得的先前证据一起,目前的结果表明,在脊索动物中,从Mesp到Nkx和HAND的心脏规范机制是保守的。

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