Lee Norman H, Haas Brian J, Letwin Noah E, Frank Bryan C, Luu Truong V, Sun Qiang, House Carrie D, Yerga-Woolwine Shane, Farms Phyllis, Manickavasagam Ezhilarasi, Joe Bina
Department of Pharmacology and Physiology, George Washington University, Washington, DC, USA.
Hypertension. 2007 Dec;50(6):1126-33. doi: 10.1161/HYPERTENSIONAHA.107.093138. Epub 2007 Oct 15.
Genetic dissection of the S rat genome has provided strong evidence for the presence of 2 interacting blood pressure quantitative trait loci (QTLs), termed QTL1 and QTL2, on rat chromosome 5. However, the identities of the underlying interacting genetic factors remain unknown. Further experiments targeted to identify the interacting genetic factors by the substitution mapping approach alone are difficult because of the interdependency of natural recombinations to occur at the 2 QTLs. We hypothesized that the interacting genetic factors underlying these 2 QTLs may interact at the level of gene transcription and thereby represent expression QTLs or eQTLs. To detect these interacting expression QTLs, a custom QTL chip containing the annotated genes within QTL1 and QTL2 was developed and used to conduct a transcriptional profiling study of S and 2 congenic strains that retain either 1 or both of the QTLs. The results uncovered an interaction between 2 transcription factor genes, Dmrta2 and Nfia. Furthermore, the "biological signature" elicited by these 2 transcription factors was differential between the congenic strain that retained Lewis alleles at both QTL1 and QTL2 compared with the congenic strain that retained Lewis alleles at QTL1 alone. A network of transcription factors potentially affecting blood pressure could be traced, lending support to our hypothesis.
对S大鼠基因组的遗传剖析为大鼠5号染色体上存在两个相互作用的血压数量性状基因座(QTL)提供了有力证据,这两个基因座分别称为QTL1和QTL2。然而,潜在的相互作用遗传因素的具体身份仍然未知。由于自然重组在这两个QTL处发生的相互依赖性,仅通过替代定位方法来识别相互作用遗传因素的进一步实验具有难度。我们推测,这两个QTL潜在的相互作用遗传因素可能在基因转录水平上相互作用,因此代表表达QTL或eQTL。为了检测这些相互作用的表达QTL,我们开发了一种定制的QTL芯片,该芯片包含QTL1和QTL2内的注释基因,并用于对S大鼠和两个保留其中一个或两个QTL的近交系进行转录谱研究。结果揭示了两个转录因子基因Dmrta2和Nfia之间的相互作用。此外,与仅在QTL1处保留Lewis等位基因的近交系相比,在QTL1和QTL2处均保留Lewis等位基因的近交系中,这两个转录因子引发的“生物学特征”存在差异。可以追踪到一个可能影响血压的转录因子网络,这支持了我们的假设。