Exploration of the cell-cycle genes found within the RIKEN FANTOM2 data set

被引:12
作者
Forrest, ARR [1 ]
Taylor, D
Grimmond, S
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Australian Res Council Special Res Ctr Funct & Ap, Brisbane, Qld 4072, Australia
[3] RIKEN, Genom Sci Ctr GSC, Yokohama Inst, Lab Genome Explorat Res Grp,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[4] RIKEN, Genome Sci Lab, Wako, Saitama 3510198, Japan
关键词
D O I
10.1101/gr.1012403
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
The cell cycle is one of the most fundamental processes within a cell. Phase-dependent expression and cell-cycle checkpoints require a high level of control. A large number of genes with varying functions and modes of action are responsible for this biology. In a targeted exploration of the FANTOM2-Variable Protein Set, a number of mouse homologs to known cell-cycle regulators as well as novel members of cell-cycle families were identified. Focusing on two prototype cell-cycle families, the cyclins and the NIMA-related kinases (NEKs), we believe we have identified all of the mouse members of these families, 24 cyclins and 10 NEKs, and mapped them to ENSEMBL transcripts. To attempt to globally identify all potential cell cycle-related genes within mouse, the MGI (Mouse Genome Database) assignments for the RIKEN Representative Set (RPS) and the results from two homology-based queries were merged. We identified 1415 genes with possible cell-cycle roles, and 1758 potential paralogs. We comment on the genes identified in this screen and evaluate the merits of each approach.
引用
收藏
页码:1366 / 1375
页数:10
相关论文
共 36 条
[1]   The InterPro database, an integrated documentation resource for protein families, domains and functional sites [J].
Apweiler, R ;
Attwood, TK ;
Bairoch, A ;
Bateman, A ;
Birney, E ;
Biswas, M ;
Bucher, P ;
Cerutti, T ;
Corpet, F ;
Croning, MDR ;
Durbin, R ;
Falquet, L ;
Fleischmann, W ;
Gouzy, J ;
Hermjakob, H ;
Hulo, N ;
Jonassen, I ;
Kahn, D ;
Kanapin, A ;
Karavidopoulou, Y ;
Lopez, R ;
Marx, B ;
Mulder, NJ ;
Oinn, TM ;
Pagni, M ;
Servant, F ;
Sigrist, CJA ;
Zdobnov, EM .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :37-40
[2]  
Ashburner M, 2001, GENOME RES, V11, P1425
[3]   Dopamine and glutamate induce distinct striatal splice forms of ania-6, an RNA polymerase II-associated cyclin [J].
Berke, JD ;
Sgambato, V ;
Zhu, PP ;
Lavoie, B ;
Vincent, M ;
Krause, M ;
Hyman, SE .
NEURON, 2001, 32 (02) :277-287
[4]   Targeting the cell cycle for cancer therapy [J].
Carnero, A .
BRITISH JOURNAL OF CANCER, 2002, 87 (02) :129-133
[5]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[6]  
Dobie KW, 2001, GENETICS, V157, P1623
[7]  
ETZOLD T, 1993, COMPUT APPL BIOSCI, V9, P49
[8]   Isolation of Drosophila cyclin D, a protein expressed in the morphogenetic furrow before entry into S phase [J].
Finley, RL ;
Thomas, BJ ;
Zipursky, SL ;
Brent, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :3011-3015
[9]   Translational control of the embryonic cell cycle [J].
Groisman, I ;
Jung, MY ;
Sarkissian, M ;
Cao, QP ;
Richter, JD .
CELL, 2002, 109 (04) :473-483
[10]   Alternative splice variants of the human centrosome kinase Nek2 exhibit distinct patterns of expression in mitosis [J].
Hames, RS ;
Fry, AM .
BIOCHEMICAL JOURNAL, 2002, 361 :77-85