Pawlak Magdalena, Walkowska Agnieszka, Mlącki Michał, Pistolic Jelena, Wrzesiński Tomasz, Benes Vladimir, Jane Stephen M, Wesoły Joanna, Kompanowska-Jezierska Elżbieta, Wilanowski Tomasz
Laboratory of Signal Transduction, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Department of Renal and Body Fluid Physiology, Mossakowski Medical Research Center, Polish Academy of Sciences, Warsaw, Poland.
Acta Biochim Pol. 2015;62(2):287-96. doi: 10.18388/abp.2015_1001. Epub 2015 Apr 21.
The Grainyhead-like 1 (GRHL1) transcription factor is tissue-specific and is very highly expressed in the kidney. In humans the GRHL1 gene is located at the chromosomal position 2p25. A locus conferring increased susceptibility to essential hypertension has been mapped to 2p25 in two independent studies, but the causative gene has never been identified. Furthermore, a statistically significant association has been found between a polymorphism in the GRHL1 gene and heart rate regulation. The aim of our study was to investigate the physiological consequences of Grhl1 loss in a mouse model and ascertain whether Grhl1 may be involved in the regulation of blood pressure and heart rate.
In our research we employed the Grhl1 "knock-out" mouse strain. We analyzed renal gene expression, blood pressure and heart rate in the Grhl1-null mice in comparison with their "wild-type" littermate controls. Most important results: The expression of many genes is altered in the Grhl1(-/-) kidneys. Some of these genes have previously been linked to blood pressure regulation. Despite this, the Grhl1-null mice have normal blood pressure and interestingly, increased heart rate.
Our work did not discover any new evidence to suggest any involvement of Grhl1 in blood pressure regulation. However, we determined that the loss of Grhl1 influences the regulation of heart rate in a mouse model.
颗粒头样1(GRHL1)转录因子具有组织特异性,在肾脏中高表达。在人类中,GRHL1基因位于染色体2p25位置。在两项独立研究中,一个与原发性高血压易感性增加相关的基因座已被定位到2p25,但致病基因尚未确定。此外,已发现GRHL1基因多态性与心率调节之间存在统计学显著关联。我们研究的目的是在小鼠模型中研究Grhl1缺失的生理后果,并确定Grhl1是否可能参与血压和心率的调节。
在我们的研究中,我们使用了Grhl1“敲除”小鼠品系。我们分析了Grhl1基因敲除小鼠与它们的“野生型”同窝对照小鼠的肾脏基因表达、血压和心率。最重要的结果:许多基因的表达在Grhl1(-/-)小鼠肾脏中发生改变。其中一些基因以前与血压调节有关。尽管如此,Grhl1基因敲除小鼠的血压正常,有趣的是,心率增加。
我们的研究没有发现任何新的证据表明Grhl1参与血压调节。然而,我们确定在小鼠模型中,Grhl1的缺失会影响心率调节。