Department of Molecular and Cellular Biology, Molecular Cardiovascular Research Program, University of Arizona, Arizona 85724, USA.
Dev Biol. 2012 Aug 1;368(1):127-39. doi: 10.1016/j.ydbio.2012.05.002. Epub 2012 May 14.
The complex, partially redundant gene regulatory architecture underlying vertebrate heart formation has been difficult to characterize. Here, we dissect the primary cardiac gene regulatory network in the invertebrate chordate, Ciona intestinalis. The Ciona heart progenitor lineage is first specified by Fibroblast Growth Factor/Map Kinase (FGF/MapK) activation of the transcription factor Ets1/2 (Ets). Through microarray analysis of sorted heart progenitor cells, we identified the complete set of primary genes upregulated by FGF/Ets shortly after heart progenitor emergence. Combinatorial sequence analysis of these co-regulated genes generated a hypothetical regulatory code consisting of Ets binding sites associated with a specific co-motif, ATTA. Through extensive reporter analysis, we confirmed the functional importance of the ATTA co-motif in primary heart progenitor gene regulation. We then used the Ets/ATTA combination motif to successfully predict a number of additional heart progenitor gene regulatory elements, including an intronic element driving expression of the core conserved cardiac transcription factor, GATAa. This work significantly advances our understanding of the Ciona heart gene network. Furthermore, this work has begun to elucidate the precise regulatory architecture underlying the conserved, primary role of FGF/Ets in chordate heart lineage specification.
脊椎动物心脏形成的复杂、部分冗余的基因调控结构一直难以描述。在这里,我们剖析了无脊椎脊索动物文昌鱼的主要心脏基因调控网络。文昌鱼的心脏祖细胞谱系首先由成纤维细胞生长因子/丝裂原激活蛋白激酶 (FGF/MapK) 激活转录因子 Ets1/2 (Ets) 来指定。通过对分选的心脏祖细胞进行微阵列分析,我们在心脏祖细胞出现后不久,确定了由 FGF/Ets 上调的整套主要基因。对这些共同调控基因的组合序列分析生成了一个假设的调控代码,其中包含与特定共基序 ATTA 相关的 Ets 结合位点。通过广泛的报告基因分析,我们证实了 ATTA 共基序在心脏祖细胞基因调控中的功能重要性。然后,我们使用 Ets/ATTA 组合基序成功预测了许多其他心脏祖细胞基因调控元件,包括驱动核心保守心脏转录因子 GATAa 表达的内含子元件。这项工作极大地推进了我们对文昌鱼心脏基因网络的理解。此外,这项工作还开始阐明在脊索动物心脏谱系指定中 FGF/Ets 的保守主要作用的精确调控结构。