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Initial deployment of the cardiogenic gene regulatory network in the basal chordate Ciona intestinalis

机译:基础弦子骨质骨质基因监管网络的初步部署Ciona Intestinalis

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摘要

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.
机译:脊椎动物心肌形成底层的复杂,部分冗余的基因调节架构难以表征。在这里,我们将原发性心脏基因监管网络解剖到无脊椎动物曲线,Ciona Intestinalis。 CIONA心脏祖母血管血管血管血管血管血管血管血管血管血管血管血管血管血管血管血酶(FGF / MAPK)激活转录因子ETS1 / 2(ETS)。通过微阵列分析分类的心脏祖细胞,我们确定了心脏祖细胞出现后不久通过FGF / ETS上调的一组完整的初级基因。这些协调基因的组合序列分析产生假设的调节码,其由与特定联合主题,ATTA相关的ETS结合位点组成。通过广泛的报告分析,我们证实了ATTA CO-MOTIF在原发性心脏祖细胞基因调节中的功能重要性。然后,我们使用ETS / ATTA组合基序来成功地预测许多额外的心祖细胞基因调节元件,包括核心保守心转录因子,GATAA的内肠元素驾驶表达。这项工作显着推进了我们对CiONa心脏基因网络的理解。此外,这项工作已经开始阐明Chordate心脏谱系统规范中FGF / ETS的保守,主要作用的精确监管架构。

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