Phosphorylation of p27Kip1 on serine 10 is required for its binding to CRM1 and nuclear export.
Phosphorylation of p27Kip1 on serine 10 is required for its binding to CRM1 and nuclear export.
复制标题
DOI：
10.1074/jbc.a114.100762
复制
发表时间：
2015-03
期刊：
影响因子：
--
通讯作者：
N. Ishida;Taichi Hara;T. Kamura;Minoru Yoshida;K. Nakayama;K. Nakayama
中科院分区：
文献类型：
--
作者：
N. Ishida;Taichi Hara;T. Kamura;Minoru Yoshida;K. Nakayama;K. Nakayama
DOI 10.1074/jbc.A114.100762丝氨酸10上的p27磷酸化是其与CRM 1结合和核输出所必需的。Noriko Ishida，Taichi Hara，Takumi Kamura，Minoru Yoshida，Keiko Nakayama，and Keiichi I. Nakayama PAGE 14356：图1B包含两个错误。复制用于代表NIH 3 T3细胞的细胞质级分的抗微管蛋白免疫印迹的图像，并且还用于代表来自这些细胞的全细胞裂解物的抗微管蛋白免疫印迹。此外，用于表示来自用MG 132处理的NIH 3 T3细胞的全细胞裂解物的抗细胞周期蛋白D2免疫印迹的图像（数据未显示）也用于表示来自未处理细胞的抗细胞周期蛋白D2免疫印迹。NIH 3 T3细胞的全细胞裂解物的正确抗微管蛋白和抗细胞周期蛋白D2数据如下所示。这些修正不影响对结果的解释或本工作的结论。
DOI 10.1074/jbc.A114.100762 Phosphorylation of p27 on serine 10 is required for its binding to CRM1 and nuclear export. Noriko Ishida, Taichi Hara, Takumi Kamura, Minoru Yoshida, Keiko Nakayama, and Keiichi I. Nakayama PAGE 14356: Fig. 1B contained two errors. The image used to represent the anti-tubulin immunoblot for the cytoplasmic fraction from NIH 3T3 cells was duplicated and also used to represent the anti-tubulin immunoblot from the whole cell lysates of these cells. In addition, the image used to represent the anti-cyclin D2 immunoblot for the whole cell lysates from NIH 3T3 cells that were treated with MG132 (data not shown) was also used to represent the anti-cyclin D2 immunoblot from untreated cells. The correct anti-tubulin and anti-cyclin D2 data for the whole cell lysates of NIH 3T3 cells are shown below. These corrections do not affect the interpretation of the results or the conclusions of this work.