File S1 - The Prolyl Isomerase Pin1 Regulates mRNA Levels of Genes with Short Half-Lives by Targeting Specific RNA Binding Proteins

Supporting Tables. Table S1 The primer sequences used for RT-PCR. Table S2 List of mRNAs whose abundance increased by Pin1 siRNA knockdown. Table S3 List of mRNAs whose abundance decreased by Pin1 siRNA knockdown. Table S4 ARE containing mRNAs stabilized by Pin1 siRNA knockdown. Table S5 ARE containing mRNAs destabilized by Pin1 siRNA knockdown. Table S6 Change in mRNA abundance for several genes measured by qRT-PCR. Table S7 Change in mRNA abundance for histone mRNAs measured by microarray and qRT-PCR.
(XLS)

补充表格。表S1：反转录聚合酶链式反应（RT-PCR）所用引物序列。表S2：经Pin1小干扰RNA（siRNA）敲低后丰度上调的mRNA列表。表S3：经Pin1小干扰RNA敲低后丰度下调的mRNA列表。表S4：经Pin1小干扰RNA敲低后稳定性增强的含富含AU元件（ARE）的mRNA列表。表S5：经Pin1小干扰RNA敲低后稳定性降低的含富含AU元件（ARE）的mRNA列表。表S6：经定量反转录聚合酶链式反应（qRT-PCR）检测得到的若干基因的mRNA丰度变化情况。表S7：经基因芯片（microarray）与定量反转录聚合酶链式反应（qRT-PCR）检测得到的组蛋白mRNA的丰度变化情况。（XLS）