Piñol-Roma S, Dreyfuss G
Howard Hughes Medical Institute, University of Pennsylvania School of Medicine, Philadelphia 9104-6148.
Mol Cell Biol. 1993 Sep;13(9):5762-70. doi: 10.1128/mcb.13.9.5762-5770.1993.
Heterogeneous nuclear ribonucleoprotein (hnRNP) complexes, the structures that contain heterogeneous nuclear RNA and its associated proteins, constitute one of the most abundant components of the eukaryotic nucleus. hnRNPs appear to play important roles in the processing, and possibly also in the transport, of mRNA. hnRNP C proteins (C1, M(r) of 41,000; C2, M(r) of 43,000 [by sodium dodecyl sulfate-polyacrylamide gel electrophoresis]) are among the most abundant pre-mRNA-binding proteins, and they bind tenaciously to sequences relevant to pre-mRNA processing, including the polypyrimidine stretch of introns (when it is uridine rich). C proteins are found in the nucleus during the interphase, but during mitosis they disperse throughout the cell. They have been shown previously to be phosphorylated in vivo, and they can be phosphorylated in vitro by a casein kinase type II. We have identified and partially purified at least two additional C protein kinases. One of these, termed Cs kinase, caused a distinct mobility shift of C proteins on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. These phosphorylated C proteins, the Cs proteins, were the prevalent forms of C proteins during mitosis, and Cs kinase activity was also increased in extracts prepared from mitotic cells. Thus, hnRNP C proteins undergo cell cycle-dependent phosphorylation by a cell cycle-regulated protein kinase. Cs kinase activity appears to be distinct from the well-characterized mitosis-specific histone H1 kinase activity. Several additional hnRNP proteins are also phosphorylated during mitosis and are thus also potential substrates for Cs kinase. These novel phosphorylations may be important in regulating the assembly and disassembly of hnRNP complexes and in the function or cellular localization of RNA-binding proteins.
异质性核核糖核蛋白(hnRNP)复合物是包含异质性核RNA及其相关蛋白质的结构,是真核细胞核中最丰富的成分之一。hnRNP似乎在mRNA的加工过程中发挥重要作用,可能还参与mRNA的转运。hnRNP C蛋白(C1,相对分子质量为41000;C2,相对分子质量为43000[通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定])是最丰富的前体mRNA结合蛋白之一,它们紧密结合于与前体mRNA加工相关的序列,包括内含子的多嘧啶序列(当富含尿苷时)。C蛋白在间期存在于细胞核中,但在有丝分裂期间它们会分散到整个细胞中。先前已证明它们在体内会被磷酸化,并且在体外可被II型酪蛋白激酶磷酸化。我们已经鉴定并部分纯化了至少另外两种C蛋白激酶。其中一种称为Cs激酶,它在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上导致C蛋白出现明显的迁移率变化。这些磷酸化的C蛋白,即Cs蛋白,是有丝分裂期间C蛋白的主要形式,并且Cs激酶活性在从有丝分裂细胞制备的提取物中也有所增加。因此,hnRNP C蛋白通过一种细胞周期调节的蛋白激酶进行细胞周期依赖性磷酸化。Cs激酶活性似乎与特征明确的有丝分裂特异性组蛋白H1激酶活性不同。几种其他的hnRNP蛋白在有丝分裂期间也会被磷酸化,因此也是Cs激酶的潜在底物。这些新的磷酸化可能在调节hnRNP复合物的组装和解聚以及RNA结合蛋白的功能或细胞定位方面很重要。