The evolution of Fox genes and their role in development and disease

被引:529
作者
Hannenhalli, Sridhar [1 ,2 ]
Kaestner, Klaus H. [1 ,3 ]
机构
[1] Univ Penn, Dept Genet, Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Penn Ctr Bioinformat, Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Inst Diabet Obes & Metab, Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
FORKHEAD TRANSCRIPTION FACTOR; PROTEIN-KINASE B; WINGED HELIX/FORKHEAD PROTEINS; INSULIN-RESPONSE SEQUENCE; CAENORHABDITIS-ELEGANS; DNA-BINDING; PHOSPHOENOLPYRUVATE CARBOXYKINASE; EMBRYONIC EXPRESSION; GLUCOSE-HOMEOSTASIS; DEFINITIVE ENDODERM;
D O I
10.1038/nrg2523
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The forkhead box (Fox) family of transcription factors, which originated in unicellular eukaryotes, has expanded over time through multiple duplication events, and sometimes through gene loss, to over 40 members in mammals. Fox genes have evolved to acquire a specialized function in many key biological processes. Mutations in Fox genes have a profound effect on human disease, causing phenotypes as varied as cancer, glaucoma and language disorders. We summarize the salient features of the evolution of the Fox gene family and highlight the diverse contribution of various Fox subfamilies to developmental processes, from organogenesis to speech acquisition.
引用
收藏
页码:233 / 240
页数:8
相关论文
共 96 条
[1]  
ANG SL, 1993, DEVELOPMENT, V119, P1301
[2]   HNF-3-BETA IS ESSENTIAL FOR NODE AND NOTOCHORD FORMATION IN MOUSE DEVELOPMENT [J].
ANG, SL ;
ROSSANT, J .
CELL, 1994, 78 (04) :561-574
[3]   Conservation of an insulin response unit between mouse and human glucose-6-phosphatase catalytic subunit gene promoters - Transcription factor FKHR binds the insulin response sequence [J].
Ayala, JE ;
Streeper, RS ;
Desgrosellier, JS ;
Durham, SK ;
Suwanichkul, A ;
Svitek, CA ;
Goldman, JK ;
Barr, FG ;
Powell, DR ;
O'Brien, RM .
DIABETES, 1999, 48 (09) :1885-1889
[4]  
Barr FG, 1999, CANCER RES, V59, p1711S
[5]   Impaired male fertility and atrophy of seminiferous tubules caused by haploinsufficiency for Foxa3 [J].
Behr, Ruediger ;
Sackett, Sara D. ;
Bochkis, Irina M. ;
Le, Phillip Phuc ;
Kaestner, Klaus H. .
DEVELOPMENTAL BIOLOGY, 2007, 306 (02) :636-645
[6]   Immunohistochemical localization of Foxa1 and Foxa2 in mouse embryos and adult tissues [J].
Besnard, V ;
Wert, SE ;
Hull, WM ;
Whitsett, JA .
GENE EXPRESSION PATTERNS, 2004, 5 (02) :193-208
[7]   Stage-specific regulation of respiratory epithelial cell differentiation by Foxa1 [J].
Besnard, V ;
Wert, SE ;
Kaestner, KH ;
Whitsett, JA .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2005, 289 (05) :L750-L759
[8]   Hepatocyte-specific ablation of Foxa2 alters bile acid homeostasis and results in endoplasmic reticulum stress [J].
Bochkis, Irina M. ;
Rubins, Nir E. ;
White, Peter ;
Furth, Emma E. ;
Friedman, Joshua R. ;
Kaestner, Klaus H. .
NATURE MEDICINE, 2008, 14 (08) :828-836
[9]   Comparative evolutionary analysis of the FoxG1 transcription factor from diverse vertebrates identifies conserved recognition sites for microRNA regulation [J].
Bredenkamp, Nicholas ;
Seoighe, Cathal ;
Illing, Nicola .
DEVELOPMENT GENES AND EVOLUTION, 2007, 217 (03) :227-233
[10]   Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor [J].
Brunet, A ;
Bonni, A ;
Zigmond, MJ ;
Lin, MZ ;
Juo, P ;
Hu, LS ;
Anderson, MJ ;
Arden, KC ;
Blenis, J ;
Greenberg, ME .
CELL, 1999, 96 (06) :857-868