Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, NY 14642, USA.
EMBO J. 2011 Jan 5;30(1):79-89. doi: 10.1038/emboj.2010.316. Epub 2010 Dec 3.
All pseudouridines identified in RNA are considered constitutive modifications. Here, we demonstrate that pseudouridylation of Saccharomyces cerevisiae U2 snRNA can be conditionally induced. While only Ψ35, Ψ42 and Ψ44 are detected in U2 under normal conditions, nutrient deprivation leads to additional pseudouridylation at positions 56 and 93. Pseudouridylation at position 56 can also be induced by heat shock. Detailed analyses have shown that Pus7p, a single polypeptide pseudouridylase known to modify U2 at position 35 and tRNA at position 13, catalyses Ψ56 formation, and that snR81 RNP, a box H/ACA RNP known to modify U2 snRNA at position 42 and 25S rRNA at position 1051, catalyses Ψ93 formation. Using mutagenesis, we have demonstrated that the inducibility can be attributed to the imperfect substrate sequences. By introducing Ψ93 into log-phase cells, we further show that Ψ93 has a role in pre-mRNA splicing. Our results thus demonstrate for the first time that pseudouridylation of RNA can be induced at sites of imperfect sequences, and that Pus7p and snR81 RNP can catalyse both constitutive and inducible pseudouridylation.
所有在 RNA 中鉴定出的假尿嘧啶核苷都被认为是组成型修饰。在这里,我们证明酿酒酵母 U2 snRNA 的假尿嘧啶核苷修饰可以被条件诱导。虽然在正常条件下只检测到 U2 中的 Ψ35、Ψ42 和 Ψ44,但营养剥夺会导致位置 56 和 93 处的额外假尿嘧啶核苷修饰。位置 56 的假尿嘧啶核苷修饰也可以被热休克诱导。详细分析表明,Pus7p,一种已知在位置 35 修饰 U2 和位置 13 修饰 tRNA 的单多肽假尿嘧啶核苷酶,催化 Ψ56 的形成,而 snR81 RNP,一种已知在位置 42 修饰 U2 snRNA 和位置 1051 修饰 25S rRNA 的 box H/ACA RNP,催化 Ψ93 的形成。通过突变分析,我们证明了可诱导性归因于不完全的底物序列。通过将 Ψ93 引入对数期细胞,我们进一步表明 Ψ93 在 pre-mRNA 剪接中起作用。因此,我们的研究结果首次证明了 RNA 的假尿嘧啶核苷修饰可以在不完全序列的部位被诱导,并且 Pus7p 和 snR81 RNP 可以催化组成型和诱导型假尿嘧啶核苷修饰。