Karaulanov Emil, Knöchel Walter, Niehrs Christof
Division of Molecular Embryology, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 280, Heidelberg, Germany.
EMBO J. 2004 Feb 25;23(4):844-56. doi: 10.1038/sj.emboj.7600101. Epub 2004 Feb 12.
Synexpression groups are genetic modules composed of genes that share both a complex expression pattern and the biological process in which they function. Here we investigate the regulation of BMP4 synexpression by studying the enhancers of bambi, smad7 and vent2 in Xenopus. We find that a BMP4 synexpression promoter module is compact and (i) requires direct BMP responsiveness through Smad and Smad-cofactor binding motifs, (ii) may contain an evolutionary conserved BMP-responsive element, bre7 (TGGCGCC), that is crucial for expression of bambi and smad7 and is highly prognostic for novel BMP-responsive enhancers (BREs); and (iii) requires a narrow window of BMP inducibility, because minor enhancement or reduction of BMP responsiveness abolishes synexpression. Furthermore, we used a bioinformatic model to predict in silico 13 novel BREs, and tested five of them that were found in the id1-4 genes. The results highlight that in vivo analysis is required to reveal the physiological, spatio-temporal regulation of BMP-responsive genes.
协同表达组是由共享复杂表达模式及其所发挥功能的生物学过程的基因组成的遗传模块。在此,我们通过研究非洲爪蟾中bambi、smad7和vent2的增强子来探究BMP4协同表达的调控机制。我们发现一个BMP4协同表达启动子模块结构紧凑,并且(i)需要通过Smad和Smad辅因子结合基序实现直接的BMP反应性;(ii)可能包含一个进化保守的BMP反应元件bre7(TGGCGCC),它对于bambi和smad7的表达至关重要,并且对新型BMP反应增强子(BREs)具有高度预测性;(iii)需要一个狭窄的BMP诱导窗口,因为BMP反应性的轻微增强或降低都会消除协同表达。此外,我们使用生物信息学模型在计算机上预测了13个新型BREs,并对在id1 - 4基因中发现的其中5个进行了测试。结果表明,需要进行体内分析来揭示BMP反应性基因的生理、时空调控机制。