Gu Haidong, Schoenberg Daniel R
Department of Molecular and Cellular Biochemistry and the Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Nucleic Acids Res. 2003 Nov 1;31(21):6264-71. doi: 10.1093/nar/gkg823.
The poly(A)-limiting element (PLE) restricts the length of the poly(A) tail to <20 nt when present in the terminal exon of a pre-mRNA. We previously identified a 65 kDa protein that could be cross-linked to a functional PLE, but not to an inactive mutant element. This binding was competed by poly(U) and poly(C), but not poly(A) or poly(G). Selectivity for the pyrimidine-rich portion of the PLE was demonstrated by RNase footprinting of the binding activity in total nuclear extract. A 65 kDa protein that selectively cross-linked to the functional PLE was purified by conventional chromatography and identified as the large subunit of U2 snRNP auxiliary factor (U2AF). Overexpression of U2AF65 in cells transfected with a PLE-containing reporter construct resulted in the appearance of a population of mRNAs with heterogeneous poly(A) tails. However, this effect was lost following deletion of the C-terminal RNA recognition motifs (RRMs). A C-->G mutation following the AG dinucleotide in the PLE resulted in mRNA with poly(A) ranging from 25-50 nt. This reverted to a discrete, <20 nt poly(A) tail in cells expressing U2AF65. Our results suggest that U2AF modulates the function of the PLE, perhaps by facilitating the binding of another protein to the element.
当存在于前体mRNA的末端外显子时,聚腺苷酸限制元件(PLE)会将聚腺苷酸尾的长度限制在<20个核苷酸。我们之前鉴定出一种65 kDa的蛋白质,它可以与功能性PLE交联,但不能与无活性的突变元件交联。这种结合可被聚尿苷酸(poly(U))和聚胞苷酸(poly(C))竞争,但不能被聚腺苷酸(poly(A))或聚鸟苷酸(poly(G))竞争。通过对全核提取物中结合活性的核糖核酸酶足迹分析,证明了对PLE富含嘧啶部分的选择性。通过常规色谱法纯化了一种与功能性PLE选择性交联的65 kDa蛋白质,并鉴定为U2小核核糖核蛋白辅助因子(U2AF)的大亚基。在转染了含PLE报告构建体的细胞中过表达U2AF65,导致出现一群具有异质聚腺苷酸尾的mRNA。然而,在缺失C末端RNA识别基序(RRMs)后,这种效应消失了。PLE中AG二核苷酸后的C→G突变导致mRNA的聚腺苷酸长度在25 - 50个核苷酸之间。在表达U2AF65的细胞中,这又恢复为离散的、<20个核苷酸的聚腺苷酸尾。我们的结果表明,U2AF可能通过促进另一种蛋白质与该元件的结合来调节PLE的功能。