Laskey R A
Philos Trans R Soc Lond B Biol Sci. 1983 Jul 5;302(1108):143-50. doi: 10.1098/rstb.1983.0047.
Many nuclear proteins are phosphorylated: they range from enzymes to several structural proteins such as histones, non-histone chromosomal proteins and the nuclear lamins. The pattern of phosphorylation varies through the cell cycle. Although histone H1 is phosphorylated during interphase its phosphorylation increases sharply during mitosis. Histone H3, chromosomal protein HMG 14 and lamins A, B and C all show reversible phosphorylation during mitosis. Several nuclear kinases have been characterized, including one that increases during mitosis and phosphorylates H1 in vitro. Factors have been demonstrated in maturing amphibian oocytes and mitotic mammalian cells that induce chromosome condensation and breakdown of the nuclear membrane. The possibility that they are autocatalytic protein kinases is considered. The location of histone phosphorylation sites within the nucleosome is consistent with a role for phosphorylation in modulating chromatin folding.
它们涵盖从酶到多种结构蛋白,如组蛋白、非组蛋白染色体蛋白和核纤层蛋白。磷酸化模式在细胞周期中会发生变化。虽然组蛋白H1在间期会发生磷酸化,但其磷酸化在有丝分裂期间会急剧增加。组蛋白H3、染色体蛋白HMG 14以及核纤层蛋白A、B和C在有丝分裂期间均表现出可逆的磷酸化。已鉴定出几种核激酶,包括一种在有丝分裂期间增加并在体外使H1磷酸化的激酶。在成熟的两栖类卵母细胞和有丝分裂的哺乳动物细胞中已证实存在诱导染色体凝聚和核膜破裂的因子。人们考虑了它们是自催化蛋白激酶的可能性。核小体内组蛋白磷酸化位点的位置与磷酸化在调节染色质折叠中的作用相一致。