Hlubek F, Löhberg C, Meiler J, Jung A, Kirchner T, Brabletz T
Department of Pathology, University of Erlangen-Nürnberg, Krankenhausstr. 8-10, 91054 Erlangen, Germany.
J Biochem. 2001 Apr;129(4):635-41. doi: 10.1093/oxfordjournals.jbchem.a002901.
Tip60 was originally identified as cellular HIV-Tat interacting protein and has been shown to augment Tat-dependent transcription. It has also been shown to interact with various cellular transcription factors and to belong to the nuclear histone acetyltransferase (HAT) family. To further elucidate the function of Tip60 and its HAT domain in transcription regulation, we compared Tip60 activity in HeLa and Jurkat T lymphoma cells. Here we show that Tip60 augments the HIV-1 Tat activity at the HIV-LTR promoter in HeLa but inhibits it in Jurkat cells. Moreover, we isolated two new variants of the Tip60 protein (Tip60Delta1, Tip60Delta2) from Jurkat cells. The Tip60Delta2 variant lacks the entire HAT domain but modulates HIV-1 Tat activity like full-length Tip60. In addition, Tip60 and the transcriptional repressor ZEB (zinc finger E box binding protein) interact specifically in the yeast two-hybrid system and additively inhibit the CD4 enhancer/promoter activity in Jurkat cells. Thus, Tip60 may function as corepressor of the ZEB protein. In summary, these data show that Tip60 functions as a cell-type-specific transcriptional regulator and that the HAT domain is not required for either transcriptional activation or inhibition. This indicates that Tip60 may function by recruiting additional cell-type-specific cofactors.
Tip60最初被鉴定为细胞内与HIV-Tat相互作用的蛋白,并已证明它可增强Tat依赖性转录。它还被证明能与多种细胞转录因子相互作用,属于核组蛋白乙酰转移酶(HAT)家族。为了进一步阐明Tip60及其HAT结构域在转录调控中的功能,我们比较了Tip60在HeLa细胞和Jurkat T淋巴瘤细胞中的活性。在此我们表明,Tip60在HeLa细胞中增强HIV-LTR启动子处的HIV-1 Tat活性,但在Jurkat细胞中则抑制该活性。此外,我们从Jurkat细胞中分离出Tip60蛋白的两个新变体(Tip60Delta1、Tip60Delta2)。Tip60Delta2变体缺乏整个HAT结构域,但像全长Tip60一样调节HIV-1 Tat活性。另外,Tip60与转录抑制因子ZEB(锌指E盒结合蛋白)在酵母双杂交系统中特异性相互作用,并在Jurkat细胞中协同抑制CD4增强子/启动子活性。因此,Tip60可能作为ZEB蛋白的共抑制因子发挥作用。总之,这些数据表明Tip60作为一种细胞类型特异性转录调节因子发挥作用,且转录激活或抑制均不需要HAT结构域。这表明Tip60可能通过招募其他细胞类型特异性辅因子发挥作用。