Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Diabetes, Obesity and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Endocrinology. 2023 Dec 23;165(2). doi: 10.1210/endocr/bqad197.
Mutations in CDKN1C, encoding p57KIP2, a canonical cell cycle inhibitor, underlie multiple pediatric endocrine syndromes. Despite this central role in disease, little is known about the structure and function of p57KIP2 in the human pancreatic beta cell. Since p57KIP2 is predominantly nuclear in human beta cells, we hypothesized that disease-causing mutations in its nuclear localization sequence (NLS) may correlate with abnormal phenotypes. We prepared RIP1 insulin promoter-driven adenoviruses encoding deletions of multiple disease-associated but unexplored regions of p57KIP2 and performed a comprehensive structure-function analysis of CDKN1C/p57KIP2. Real-time polymerase chain reaction and immunoblot analyses confirmed p57KIP2 overexpression, construct size, and beta cell specificity. By immunocytochemistry, wild-type (WT) p57KIP2 displayed nuclear localization. In contrast, deletion of a putative NLS at amino acids 278-281 failed to access the nucleus. Unexpectedly, we identified a second downstream NLS at amino acids 312-316. Further analysis showed that each individual NLS is required for nuclear localization, but neither alone is sufficient. In summary, p57KIP2 contains a classical bipartite NLS characterized by 2 clusters of positively charged amino acids separated by a proline-rich linker region. Variants in the sequences encoding these 2 NLS sequences account for functional p57KIP2 loss and beta cell expansion seen in human disease.
CDKN1C 基因突变导致多种儿科内分泌综合征,该基因编码细胞周期抑制剂 p57KIP2。尽管 p57KIP2 在疾病中起核心作用,但人们对其在人胰腺β细胞中的结构和功能知之甚少。由于 p57KIP2 在人β细胞中主要位于核内,我们假设其核定位序列(NLS)中的致病突变可能与异常表型相关。我们制备了 RIP1 胰岛素启动子驱动的腺病毒,编码 p57KIP2 多个疾病相关但未探索区域的缺失,并对 CDKN1C/p57KIP2 进行了全面的结构-功能分析。实时聚合酶链反应和免疫印迹分析证实了 p57KIP2 的过表达、构建体大小和β细胞特异性。通过免疫细胞化学,野生型(WT)p57KIP2 显示核定位。相比之下,缺失氨基酸 278-281 处的假定 NLS 未能进入核内。出乎意料的是,我们鉴定出第二个下游 NLS 位于氨基酸 312-316 处。进一步的分析表明,每个单独的 NLS 都需要核定位,但单独使用都不足以实现核定位。总之,p57KIP2 包含一个经典的双部分 NLS,其特征是由富含脯氨酸的连接区分隔的 2 个带正电荷氨基酸簇。这些 2 个 NLS 序列编码序列中的变异导致了人类疾病中所见的功能性 p57KIP2 缺失和β细胞扩张。