Hoare Sarasija, Hoare Kishalay, Reinhard Mary K, Flagg Tammy O, May William Stratford
Department of Internal Medicine, University of Florida Shands Cancer Center, P.O. Box No: 103633, Gainesville, FL 32610, USA.
Gene. 2009 Sep 1;444(1-2):1-9. doi: 10.1016/j.gene.2009.05.010. Epub 2009 May 27.
Tnk1/Kos1 is a non-receptor protein tyrosine kinase found to be a tumor suppressor. It negatively regulates cell growth by indirectly suppressing Ras activity. We identified and characterized the critical cis-elements required for Tnk1/Kos1's promoter activity. Results indicate that the murine Tnk1 promoter lacks a conventional TATA, CAAT or initiator element (Inr) but contains multiple transcription start sites. Transcription is initiated by a TATA-like element composed of an AT rich sequence at -30 (30 bp upstream) from the major transcription start site and an Inr-like element that overlaps the multiple start sites. Deletion analysis of the m-Tnk1 promoter reveals the presence of both positive (-25 to -151) and negative (-151 to -1201) regulatory regions. The three GC boxes which bind Sp1 and Sp3 with high affinity, an AP2 site (that overlaps with an AML1 site) and a MED1 site comprise the necessary cis-elements of the proximal promoter required for both constitutive and inducible Tnk1/Kos1 expression. Importantly, results reveal that cellular stress reverses the repression of Tnk1/Kos1 and induces its expression through increased high affinity interactions between nuclear proteins Sp1, Sp3, AP2 and MED1 for the m-Tnk1 promoter. These findings provide a mechanism by which the m-Tnk1 promoter can be dynamically regulated during normal growth.
Tnk1/Kos1是一种非受体蛋白酪氨酸激酶,被发现具有肿瘤抑制作用。它通过间接抑制Ras活性来负向调节细胞生长。我们鉴定并表征了Tnk1/Kos1启动子活性所需的关键顺式元件。结果表明,小鼠Tnk1启动子缺乏传统的TATA、CAAT或起始子元件(Inr),但包含多个转录起始位点。转录由一个类似TATA的元件启动,该元件由位于主要转录起始位点上游30个碱基对(-30)处的富含AT的序列和一个与多个起始位点重叠的类似Inr的元件组成。对m-Tnk1启动子的缺失分析揭示了正调控区域(-25至-151)和负调控区域(-151至-1201)的存在。三个与Sp1和Sp3具有高亲和力结合的GC框、一个AP2位点(与AML1位点重叠)和一个MED1位点构成了组成型和诱导型Tnk1/Kos1表达所需的近端启动子的必要顺式元件。重要的是,结果表明细胞应激可逆转Tnk1/Kos1的抑制作用,并通过核蛋白Sp1、Sp3、AP2和MED1与m-Tnk1启动子之间增加的高亲和力相互作用诱导其表达。这些发现提供了一种机制,通过该机制m-Tnk1启动子在正常生长过程中可被动态调节。