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Common role for each of the cGATA-4/5/6 genes in the regulation of cardiacmorphogenesis

机译:每个cGATA-4 / 5/6基因在调节心脏形态发生中的共同作用

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摘要

The GATA-4/5/6 genes encode transcription factors implicated previously in the regulation of cardiac-specific differentiation programs. However, recent analyses of mouse GATA-4 null mutations found evidence For function in endoderm development (in vitro) and embryonic morphogenesis (in vivo). Whether each of the three cardiac-associated GATA factors Function within distinct or common developmental programs grams was previously untested, past studies defined specific and distinct roles for each of the GATA-1/2/3 genes in embryonic hematopoiesis. in this study, we compare the transcript patterns of cGATA-4/5/6 during chick embryogenesis. Each of the three GATA factors is expressed in a similar pattern within gastrulating cells of the primitive streak, prior to determination of the cardiomyocyte progenitors, and later within the lateral plate mesoderm and associated endoderm layer. The patterns overlap but extend beyond the presumptive cardiomyocyte population expressing cNkx-2.5. later in develop ment, cGATA-4/5/6 are ail transcribed throughout the differentiating heart, in similar but not identical patterns, within the endocardium, myocardium, and great vessels. In order to test the function of GATA factors during chick cardiogenesis, embryos were cultured in vitro in the presence of antisense oligomers designed to deplete specifically transcripts encoding cGATA-4/5/6, beginning around stage 7. When oligomers are used to target transcripts For ail three genes, a high percentage of the embryos develop abnormal hearts related to the failure to form a normal primitive heart tube. In the most severe phenotype, cardiac bifida results in two bilateral beating hearts. In some embryos, the paired heart primordia undergo partial fusion but fail to form a single looping heart tube. In all cases, cellular differentiation is not obviously affected, as the abnormal hearts Form beating tissue. Depletion of transcripts encoding any single GATA factor, or any combination of two GATA Factors, does not affect development. The partial depletion of all three genes in chick results In a remarkably similar phenotype compared to the null GATA-4 mutation in mouse. Therefore, in the chick, each of the GATA-4/5/6 genes functions in a common pathway, at the time of cardiac crescent Formation, for regulating early embryonic cardiac morphogenesis, apparently associated with embryonic folding or the migration of primordia to Form a primitive tube.
机译:GATA-4 / 5/6基因编码先前参与心脏特异性分化程序调控的转录因子。但是,最近对小鼠GATA-4无效突变的分析发现了内胚层发育(体外)和胚胎形态发生(体内)功能的证据。之前是否未经测试过三种与心脏相关的GATA因子在不同的或共同的发育程序中的功能,过去的研究为胚胎造血中的每个GATA-1 / 2/3基因定义了特定而独特的作用。在这项研究中,我们比较了鸡胚发生过程中cGATA-4 / 5/6的转录模式。在确定心肌细胞祖细胞之前,三个GATA因子中的每一个均以相似的模式在原始条纹的胃化细胞中表达,随后在外侧板中胚层和相关的内胚层中表达。模式重叠但延伸到表达cNkx-2.5的推测心肌细胞群之外。在开发的后期,cGATA-4 / 5/6会以相似但不相同的模式在心内膜,心肌和大血管中全部转录到整个分化的心脏中。为了测试GATA因子在小鸡心脏发生过程中的功能,在存在反义寡聚体的情况下体外培养了胚胎,该寡聚体旨在从7阶段开始耗尽编码cGATA-4 / 5/6的特异性转录本。当使用寡聚体靶向转录本时对于所有三个基因,高比例的胚胎会发育异常的心脏,这与无法形成正常的原始心管有关。在最严重的表型中,心脏双歧杆菌会导致两个双侧跳动的心脏。在某些胚胎中,成对的心脏原基经历部分融合,但无法形成单个环状的心管。在所有情况下,由于异常心脏形成搏动组织,因此细胞分化并未受到明显影响。编码任何单个GATA因子或两个GATA因子的任意组合的转录本的耗尽均不会影响发育。与小鼠的空GATA-4突变相比,雏鸡中所有三个基因的部分耗竭导致表型显着相似。因此,在雏鸡中,每个GATA-4 / 5/6基因在心脏新月形成时均以共同的途径起作用,以调节早期胚胎的心脏形态发生,这显然与胚胎折叠或原基向表皮的迁移有关。原始管。

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