Steen Rikke L, Beullens Monique, Landsverk Helga B, Bollen Mathieu, Collas Philippe
Institute of Medical Biochemistry, University of Oslo, PO Box 1112 Blindern, 0317 Oslo, Norway.
J Cell Sci. 2003 Jun 1;116(Pt 11):2237-46. doi: 10.1242/jcs.00432. Epub 2003 Apr 15.
Reassembly of the nuclear envelope (NE) at the end of mitosis requires targeting of the B-type lamin protein phosphatase, PP1, to the envelope by A-kinase anchoring protein AKAP149. We show here that NE-associated AKAP149 is a novel PP1-specifying subunit involved in maintaining nuclear architecture through G1 phase. PP1 remains associated with NE-bound AKAP149 during G1 but is released from AKAP149 upon S phase entry, as AKAP149 becomes serine-phosphorylated. NE-associated AKAP149 inhibits PP1 activity towards glycogen phosphorylase but enhances PP1 phosphatase activity towards B-type lamins, indicating that AKAP149 is a B-type lamin specifying subunit of PP1. In vivo dissociation of PP1 from NE-bound AKAP149 in G1-phase nuclei triggers phosphorylation and depolymerization of A- and B-type lamins. The lamins solubilize intranuclearly without affecting the inner nuclear membrane or pore complex distribution. This correlates with the induction of a G1 arrest and, ultimately, apoptosis. We propose that AKAP149-regulated PP1 activity at the NE during G1 is required to maintain nuclear integrity and cell survival.
有丝分裂末期核膜(NE)的重新组装需要A激酶锚定蛋白AKAP149将B型核纤层蛋白磷酸酶PP1靶向至核膜。我们在此表明,与核膜相关的AKAP149是一种新型的PP1特异性亚基,通过G1期参与维持核结构。在G1期,PP1仍与结合在核膜上的AKAP149相关联,但在进入S期时从AKAP149上释放,因为AKAP149发生了丝氨酸磷酸化。与核膜相关的AKAP149抑制PP1对糖原磷酸化酶的活性,但增强PP1对B型核纤层蛋白的磷酸酶活性,表明AKAP149是PP1的B型核纤层蛋白特异性亚基。在体内,G1期细胞核中PP1与结合在核膜上的AKAP149解离会触发A 型和B型核纤层蛋白的磷酸化和解聚。核纤层蛋白在核内溶解,而不影响内核膜或核孔复合体的分布。这与G1期阻滞的诱导以及最终的细胞凋亡相关。我们提出,G1期核膜处AKAP149调节的PP1活性对于维持核完整性和细胞存活是必需的。