Liu C J, Wang H, Lengyel P
Department of Molecular Biophysics and Biochemistry, Yale University, PO Box 208024, 333 Cedar Street, New Haven, CT 06520-8024, USA.
EMBO J. 1999 May 17;18(10):2845-54. doi: 10.1093/emboj/18.10.2845.
p204, a member of the interferon-inducible p200 family of murine proteins, is primarily nucleolar. We generated cell lines in which p204 was inducible by muristerone. This induction resulted in retardation of cell proliferation and inhibition of rRNA transcription in vivo. Interferon treatment, resulting in p204 induction and retardation of proliferation, also caused inhibition of rRNA transcription in vivo. p204 also inhibited rRNA transcription in vitro. This inhibition was overcome by addition of UBF1, the rRNA-specific transcription factor. A direct interaction between p204 and UBF1 was revealed in vitro in pull-down assays, and in vivo by co-immunoprecipitation from cell extracts. UBF1 bound strongly to at least two regions of p204: the N-terminal segment linked to the conserved 200 amino acid a segment, and the conserved 200 amino acid b segment. Cleavage of the a or b segments into two segments (encoded by single exons) resulted in a strong decrease or loss of binding. The inhibition of rRNA transcription by p204 may be due to the inhibition by p204 of the specific DNA binding of UBF1. This was revealed in electrophoretic mobility shift, magnetic bead and footprinting assays. Thus, p204 serves as a mediator of the inhibition of rRNA transcription by interferon.
p204是小鼠干扰素诱导的p200蛋白家族的成员之一,主要定位于核仁。我们构建了p204可被孕诺酮诱导的细胞系。这种诱导导致体内细胞增殖迟缓以及rRNA转录受到抑制。干扰素处理可诱导p204表达并使增殖迟缓,同时也会导致体内rRNA转录受到抑制。p204在体外也能抑制rRNA转录。添加rRNA特异性转录因子UBF1可克服这种抑制作用。在体外下拉试验以及从细胞提取物中进行的体内共免疫沉淀试验均显示p204与UBF1之间存在直接相互作用。UBF1与p204的至少两个区域紧密结合:与保守的200个氨基酸a片段相连的N端片段,以及保守的200个氨基酸b片段。将a或b片段切割成两个片段(由单个外显子编码)会导致结合力大幅下降或丧失。p204对rRNA转录的抑制作用可能是由于p204抑制了UBF1与特异性DNA的结合。这在电泳迁移率变动分析、磁珠分析和足迹分析中得到了证实。因此,p204作为干扰素抑制rRNA转录的介质发挥作用。