The RIO kinases: An atypical protein kinase family required for ribosome biogenesis and cell cycle progression

被引:92
作者
LaRonde-LeBlanc, N [1 ]
Wlodawer, A [1 ]
机构
[1] NCI, Prot Struct Sect, Macromol Crystallog Lab, Frederick, MD 21702 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2005年 / 1754卷 / 1-2期
关键词
atypical protein kinase; structure; ATP binding; enzymatic activity; ribosome biogenesis; Rio1; Rio2;
D O I
10.1016/j.bbapap.2005.07.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atypical protein kinases (aPKs) include proteins known to be involved in the phosphorylation-mediated regulation of a wide variety of cellular processes, as well as some for which the function is, as yet, unknown. At present, 13 families of aPKs have been identified in the human genome. This review briefly summarizes their known properties, but concentrates in particular on the RIO family of aPKs. Representatives of this family are present in organisms varying from archaea to humans. All these organisms contain at least two RIO proteins, Rio1 and Rio2, but a third Rio3 group is present in multicellular eukaryotes. Crystal structures of A. fulgidus Rio I and Rio2 have shown that whereas the overall fold of these enzymes resembles typical protein kinases, some of the kinase structural domains, particularly those involved in peptide substrate binding, are not present. The mode of binding of nucleotides also differs from other kinases. While the enzymatic activity of Rio I and Rio2 has been demonstrated and both have been shown to be essential in S. cerevisiae and required for proper cell cycle progression and chromosome maintenance, the biological substrates of RIO proteins still remain to be identified. Published by Elsevier B.V.
引用
收藏
页码:14 / 24
页数:11
相关论文
共 50 条
[1]   PI 3-kinase related kinases: 'big' players in stress-induced signaling pathways [J].
Abraham, RT .
DNA REPAIR, 2004, 3 (8-9) :883-887
[2]   Isolation of the Aspergillus nidulans sudD gene and its human homologue [J].
Anaya, P ;
Evans, SC ;
Dai, CP ;
Lozano, G ;
May, GS .
GENE, 1998, 211 (02) :323-329
[3]   RIO1, an extraordinary novel protein kinase [J].
Angermayr, M ;
Bandlow, W .
FEBS LETTERS, 2002, 524 (1-3) :31-36
[4]   Yeast Rio1p is the founding member of a novel subfamily of protein serine kinases involved in the control of cell cycle progression [J].
Angermayr, M ;
Roidl, A ;
Bandlow, W .
MOLECULAR MICROBIOLOGY, 2002, 44 (02) :309-324
[5]   PROKARYOTIC EXPRESSION CLONING OF A NOVEL HUMAN TYROSINE KINASE [J].
BEELER, JF ;
LAROCHELLE, WJ ;
CHEDID, M ;
TRONICK, SR ;
AARONSON, SA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (02) :982-988
[6]   Mapping of the novel protein kinase catalytic domain of Dictyostelium myosin II heavy chain kinase A [J].
Cote, GP ;
Luo, X ;
Murphy, MB ;
Egelhoff, TT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (11) :6846-6849
[7]  
Denis GV, 2000, CELL GROWTH DIFFER, V11, P417
[8]   A novel, mitogen-activated nuclear kinase is related to a Drosophila developmental regulator [J].
Denis, GV ;
Green, MR .
GENES & DEVELOPMENT, 1996, 10 (03) :261-271
[9]   TAF(11)250 is a bipartite protein kinase that phosphorylates the basal transcription factor RAP74 [J].
Dikstein, R ;
Ruppert, S ;
Tjian, R .
CELL, 1996, 84 (05) :781-790
[10]   Structure of the La motif: a winged helix domain mediates RNA binding via a conserved aromatic patch [J].
Dong, G ;
Chakshusmathi, G ;
Wolin, SL ;
Reinisch, KM .
EMBO JOURNAL, 2004, 23 (05) :1000-1007