Jiang Jieyun, Creasy Kate Townsend, Purnell Justin, Peterson Martha L, Spear Brett T
From the Department of Microbiology, Immunology, and Molecular Genetics,
Department of Pharmacology and Nutritional Sciences, and.
J Biol Chem. 2017 Apr 21;292(16):6765-6774. doi: 10.1074/jbc.M116.768275. Epub 2017 Mar 3.
The mouse major urinary proteins (Mups) are encoded by a large family of highly related genes clustered on chromosome 4. Mups, synthesized primarily and abundantly in the liver and secreted through the kidneys, exhibit male-biased expression. Mups bind a variety of volatile ligands; these ligands, and Mup proteins themselves, influence numerous behavioral traits. Although urinary Mup protein levels vary between inbred mouse strains, this difference is most pronounced in BALB/cJ mice, which have dramatically low urinary Mup levels; this BALB/cJ trait had been mapped to a locus on chromosome 15. We previously identified Zhx2 (zinc fingers and homeoboxes 2) as a regulator of numerous liver-enriched genes. is located on chromosome 15, and a natural hypomorphic mutation in the BALB/cJ allele dramatically reduces Zhx2 expression. Based on these data, we hypothesized that reduced Zhx2 levels are responsible for lower Mup expression in BALB/cJ mice. Using both transgenic and knock-out mice along with assays, our data show that Zhx2 binds Mup promoters and is required for high levels of Mup expression in the adult liver. In contrast to previously identified Zhx2 targets that appear to be repressed by Zhx2, Mup genes are positively regulated by Zhx2. These data identify Zhx2 as a novel regulator of Mup expression and indicate that Zhx2 activates as well as represses expression of target genes.
小鼠主要尿蛋白(Mups)由聚集在4号染色体上的一大类高度相关基因编码。Mups主要在肝脏中大量合成,并通过肾脏分泌,表现出雄性偏向性表达。Mups结合多种挥发性配体;这些配体以及Mup蛋白本身会影响众多行为特征。尽管近交系小鼠品系之间的尿Mup蛋白水平有所不同,但这种差异在BALB/cJ小鼠中最为明显,其尿Mup水平极低;这种BALB/cJ特征已被定位到15号染色体上的一个位点。我们之前鉴定出锌指和同源框2(Zhx2)是众多肝脏富集基因的调节因子。它位于15号染色体上,BALB/cJ等位基因中的一个天然低表达突变显著降低了Zhx2的表达。基于这些数据,我们推测Zhx2水平降低是BALB/cJ小鼠中Mup表达较低的原因。通过使用转基因和基因敲除小鼠以及相关实验,我们的数据表明Zhx2结合Mup启动子,并且是成年肝脏中高水平Mup表达所必需的。与之前鉴定出的似乎被Zhx2抑制的Zhx2靶标不同,Mup基因受到Zhx2的正向调节。这些数据确定Zhx2是Mup表达的一种新型调节因子,并表明Zhx2既能激活也能抑制靶基因的表达。