Gao B, Jiang L, Kunos G
Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298, USA.
Mol Cell Biol. 1996 Nov;16(11):5997-6008. doi: 10.1128/MCB.16.11.5997.
The 5' upstream region from --490 to --540 (footprint II) within the dominant P2 promoter of the rat alpha(1b) adrenergic receptor (alpha(1b)AR) gene is recognized by a sequence-specific DNA-binding protein (B. Gao, M. S. Spector, and G. Kunos, J. Biol. Chem. 270:5614-5619, 1995). This protein, detectable in Southwestern (DNA-protein) blots of crude nuclear extracts as 32- and 34-kDa bands, has been purified 6,000-fold from rat livers by DEAE-Sepharose, heparin-Sepharose, and DNA affinity chromatography. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and UV cross-linking of the purified protein indicated the same molecular mass as that in crude extracts. Methylation interference analysis revealed strong contact with a TTGGCT hexamer and weak contact with a TGGCGT hexamer in the 3' and 5' portions of footprint II, respectively. Nucleotide substitutions within these hexamers significantly reduced protein binding to footprint II and the promoter activity of P2 in Hep3B cells. The purified protein also bound to the nuclear factor 1 (NF1)/CTF consensus sequence, albeit with lower affinity. Gel mobility supershift and Western blotting (immunoblotting) analyses using an antibody against the NF1/CTF protein identified the purified 32- and 34-kDa polypeptides as NF1 or a related protein. Cotransfection into Hep3B cells or primary rat hepatocytes of cDNAs of the NF1-like proteins NF1/L, NF1/X, and NF1/Redl resulted in a three- to fivefold increase in transcription directed by wild-type P2 but not by the mutated P2. Partial hepatectomy markedly decreased the levels of NF1 in the remnant liver and its binding to P2, which paralleled declines in the rate of transcription of the alpha(1b)AR gene and in the steady-state levels of its mRNA. These observations indicate that NF1 activates transcription of the rat alpha(1b)AR gene via interacting with its P2 promoter and that a decline in the expression of NF1 is one of the mechanisms responsible for the reduced expression of the alpha(1b)AR gene during liver regeneration.
大鼠α(1b)肾上腺素能受体(α(1b)AR)基因的显性P2启动子中,从-490至-540(足迹II)的5'上游区域可被一种序列特异性DNA结合蛋白识别(B. Gao、M. S. Spector和G. Kunos,《生物化学杂志》270:5614 - 5619,1995年)。这种蛋白在粗核提取物的西南(DNA - 蛋白质)印迹中表现为32 kDa和34 kDa的条带,已通过DEAE - 琼脂糖、肝素 - 琼脂糖和DNA亲和层析从大鼠肝脏中纯化了6000倍。纯化蛋白的十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳和紫外线交联显示其分子量与粗提取物中的相同。甲基化干扰分析表明,在足迹II的3'和5'部分,该蛋白分别与TTGGCT六聚体有强相互作用,与TGGCGT六聚体有弱相互作用。这些六聚体内的核苷酸取代显著降低了蛋白与足迹II的结合以及P2在Hep3B细胞中的启动子活性。纯化蛋白也能与核因子1(NF1)/CTF共有序列结合,尽管亲和力较低。使用针对NF1/CTF蛋白的抗体进行凝胶迁移超迁移和蛋白质印迹(免疫印迹)分析,确定纯化的32 kDa和34 kDa多肽为NF1或相关蛋白。将NF1样蛋白NF1/L、NF1/X和NF1/Redl的cDNA共转染到Hep3B细胞或原代大鼠肝细胞中,导致野生型P2指导的转录增加三到五倍,而突变型P2则无此现象。部分肝切除显著降低了残余肝脏中NF1的水平及其与P2的结合,这与α(1b)AR基因转录速率和其mRNA稳态水平的下降相平行。这些观察结果表明,NF1通过与其P2启动子相互作用激活大鼠α(1b)AR基因的转录,并且NF1表达的下降是肝脏再生过程中α(1b)AR基因表达降低的机制之一。