Zentrum für Molekulare Neurobiologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.
Keck Center for Collaborative Neuroscience, Department of Cell Biology and Neuroscience, Rutgers University, 604 Allison Road, Piscataway, NJ 08854, USA.
Int J Mol Sci. 2023 Jan 4;24(2):932. doi: 10.3390/ijms24020932.
Abnormal functions of the cell adhesion molecule L1 are linked to several neural diseases. Proteolytic L1 fragments were reported to interact with nuclear and mitochondrial proteins to regulate events in the developing and the adult nervous system. Recently, we identified a 55 kDa L1 fragment (L1-55) that interacts with methyl CpG binding protein 2 (MeCP2) and heterochromatin protein 1 (HP1) via the KDET motif. We now show that L1-55 also interacts with histone H1.4 (HistH1e) via this motif. Moreover, we show that this motif binds to NADH dehydrogenase ubiquinone flavoprotein 2 (NDUFV2), splicing factor proline/glutamine-rich (SFPQ), the non-POU domain containing octamer-binding protein (NonO), paraspeckle component 1 (PSPC1), WD-repeat protein 5 (WDR5), heat shock cognate protein 71 kDa (Hsc70), and synaptotagmin 1 (SYT1). Furthermore, applications of HistH1e, NDUFV2, SFPQ, NonO, PSPC1, WDR5, Hsc70, or SYT1 siRNAs or a cell-penetrating KDET-carrying peptide decrease L1-dependent neurite outgrowth and the survival of cultured neurons. These findings indicate that L1's KDET motif binds to an unexpectedly large number of molecules that are essential for nervous system-related functions, such as neurite outgrowth and neuronal survival. In summary, L1 interacts with cytoplasmic, nuclear and mitochondrial proteins to regulate development and, in adults, the formation, maintenance, and flexibility of neural functions.
细胞黏附分子 L1 的异常功能与多种神经疾病有关。已有报道称,蛋白水解 L1 片段与核蛋白和线粒体蛋白相互作用,调节发育中和成年期神经系统中的事件。最近,我们鉴定出一种 55 kDa 的 L1 片段(L1-55),它通过 KDET 基序与甲基 CpG 结合蛋白 2(MeCP2)和异染色质蛋白 1(HP1)相互作用。我们现在表明,L1-55 也通过该基序与组蛋白 H1.4(HistH1e)相互作用。此外,我们表明该基序与 NADH 脱氢酶泛醌黄素蛋白 2(NDUFV2)、剪接因子脯氨酸/谷氨酰胺富含(SFPQ)、非 POUS 域结合八聚体结合蛋白(NonO)、核仁小核糖核蛋白成分 1(PSPC1)、WD 重复蛋白 5(WDR5)、热休克同源蛋白 71 kDa(Hsc70)和突触结合蛋白 1(SYT1)结合。此外,应用 HistH1e、NDUFV2、SFPQ、NonO、PSPC1、WDR5、Hsc70 或 SYT1 的 siRNA 或穿膜 KDET 携带肽会降低 L1 依赖性神经突生长和培养神经元的存活。这些发现表明,L1 的 KDET 基序与许多对与神经系统相关的功能(如神经突生长和神经元存活)至关重要的分子结合。总之,L1 与细胞质、核蛋白和线粒体蛋白相互作用,以调节发育,并在成年期调节神经功能的形成、维持和灵活性。