Evolution of the Fgf and Fgfr gene families

被引:930
作者
Itoh, N [1 ]
Ornitz, DM
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Biochem Genet, Kyoto 6068501, Japan
[2] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tig.2004.08.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fibroblast growth factors (Fgfs) and Fgf receptors (Fgfrs) comprise a signaling system that is conserved throughout metazoan evolution. Twenty-two Fgfs and four Fgfrs have been identified in humans and mice. During evolution, the Fgf family appears to have expanded in two phases. In the first phase, during early metazoan evolution, Fgfs expanded from two or three to six genes by gene duplication. In the second phase, during the evolution of early vertebrates, the Fgf family expanded by two large-scale gen(om)e duplications. By contrast, the Fgfr family has expanded only in the second phase. However, the acquisition of alternative splicing by Fgfrs has increased their functional diversity. The mechanisms that regulate alternative splicing have been conserved since the divergences of echinoderms and vertebrates. The expansion of the Fgf and Fgfr gene families has enabled this signaling system to acquire functional diversity and, therefore, an almost ubiquitous involvement in developmental and physiological processes.
引用
收藏
页码:563 / 569
页数:7
相关论文
共 28 条
[1]   Spatial and temporal expression of heparan sulfate in mouse development regulates FGF and FGF receptor assembly [J].
Allen, BL ;
Rapraeger, AC .
JOURNAL OF CELL BIOLOGY, 2003, 163 (03) :637-648
[2]   Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes [J].
Aparicio, S ;
Chapman, J ;
Stupka, E ;
Putnam, N ;
Chia, J ;
Dehal, P ;
Christoffels, A ;
Rash, S ;
Hoon, S ;
Smit, A ;
Gelpke, MDS ;
Roach, J ;
Oh, T ;
Ho, IY ;
Wong, M ;
Detter, C ;
Verhoef, F ;
Predki, P ;
Tay, A ;
Lucas, S ;
Richardson, P ;
Smith, SF ;
Clark, MS ;
Edwards, YJK ;
Doggett, N ;
Zharkikh, A ;
Tavtigian, SV ;
Pruss, D ;
Barnstead, M ;
Evans, C ;
Baden, H ;
Powell, J ;
Glusman, G ;
Rowen, L ;
Hood, L ;
Tan, YH ;
Elgar, G ;
Hawkins, T ;
Venkatesh, B ;
Rokhsar, D ;
Brenner, S .
SCIENCE, 2002, 297 (5585) :1301-1310
[3]   Zebraf ish fgf24 functions with fgf8 to promote posterior mesodermal development [J].
Draper, BW ;
Stock, DW ;
Kimmel, CB .
DEVELOPMENT, 2003, 130 (19) :4639-4654
[4]  
ENSOLI B, 2003, CYTOKINE HDB, P748
[5]   Genome sequence of the Brown Norway rat yields insights into mammalian evolution [J].
Gibbs, RA ;
Weinstock, GM ;
Metzker, ML ;
Muzny, DM ;
Sodergren, EJ ;
Scherer, S ;
Scott, G ;
Steffen, D ;
Worley, KC ;
Burch, PE ;
Okwuonu, G ;
Hines, S ;
Lewis, L ;
DeRamo, C ;
Delgado, O ;
Dugan-Rocha, S ;
Miner, G ;
Morgan, M ;
Hawes, A ;
Gill, R ;
Holt, RA ;
Adams, MD ;
Amanatides, PG ;
Baden-Tillson, H ;
Barnstead, M ;
Chin, S ;
Evans, CA ;
Ferriera, S ;
Fosler, C ;
Glodek, A ;
Gu, ZP ;
Jennings, D ;
Kraft, CL ;
Nguyen, T ;
Pfannkoch, CM ;
Sitter, C ;
Sutton, GG ;
Venter, JC ;
Woodage, T ;
Smith, D ;
Lee, HM ;
Gustafson, E ;
Cahill, P ;
Kana, A ;
Doucette-Stamm, L ;
Weinstock, K ;
Fechtel, K ;
Weiss, RB ;
Dunn, DM ;
Green, ED .
NATURE, 2004, 428 (6982) :493-521
[6]   FGF8-like1 and FGF8-like2 encode putative ligands of the FGF receptor Htl for mesoderm migration and are required in the Drosophila gastrula [J].
Gryzik, T ;
Müller, HAJ .
CURRENT BIOLOGY, 2004, 14 (08) :659-667
[7]   Phylogenetic analyses alone are insufficient to determine whether genome duplication(s) occurred during early vertebrate evolution [J].
Horton, AC ;
Mahadevan, NR ;
Ruvinsky, I ;
Gibson-Brown, JJ .
JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION, 2003, 299B (01) :41-53
[8]   The human FGF gene family: chromosome location and phylogenetic analysis [J].
Kim, HS .
CYTOGENETICS AND CELL GENETICS, 2001, 93 (1-2) :131-132
[9]   Fgf3 and Fgf8 dependent and independent transcription factors are required for otic placode specification [J].
Liu, D ;
Chu, H ;
Maves, L ;
Yan, YL ;
Morcos, PA ;
Postlethwait, JH ;
Westerfield, M .
DEVELOPMENT, 2003, 130 (10) :2213-2224
[10]   Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18 [J].
Liu, ZH ;
Xu, JS ;
Colvin, JS ;
Ornitz, DM .
GENES & DEVELOPMENT, 2002, 16 (07) :859-869