Update of human and mouse forkhead box (FOX) gene families.

作者: Brian C. Jackson , Christopher Carpenter , Daniel W. Nebert , Vasilis Vasiliou

DOI: 10.1186/1479-7364-4-5-345

关键词: GeneticsGene familyGene duplicationFOX proteinsTranscription factorGeneFOXM1BiologyHuman genomeGene expression

摘要: The forkhead box (FOX) proteins are transcription factors that play complex and important roles in processes from development organogenesis to regulation of metabolism the immune system. There 50 FOX genes human genome 44 mouse, divided into 19 subfamilies. All have close mouse orthologues, with one exception: has a single Foxd4, whereas gene undergone recent duplication total seven (FOXD4 FOXD4L1 → FOXD4L6). Evolutionarily ancient family members can be found as far back fungi metazoans. DNA-binding domain, is an example winged-helix very well conserved across species, few notable exceptions which divergence created new functionality. Mutations been implicated at least four familial diseases, differential expression may role number other pathologies -- ranging metabolic disorders autoimmunity. Furthermore, differentially expressed large cancers; their either oncogene or tumour suppressor, depending on member cell type. Although some drugs target activity, notably proteasome inhibitors, appear work well, much more basic research needed unlock interplay upstream downstream interactions factors.

参考文章(29)
Jun Nakae, Tadahiro Kitamura, Yukari Kitamura, William H. Biggs, Karen C. Arden, Domenico Accili, The Forkhead Transcription Factor Foxo1 Regulates Adipocyte Differentiation Developmental Cell. ,vol. 4, pp. 119- 129 ,(2003) , 10.1016/S1534-5807(02)00401-X
Lisa Ann Cirillo, Frank Robert Lin, Isabel Cuesta, Dara Friedman, Michal Jarnik, Kenneth S Zaret, Opening of Compacted Chromatin by Early Developmental Transcription Factors HNF3 (FoxA) and GATA-4 Molecular Cell. ,vol. 9, pp. 279- 289 ,(2002) , 10.1016/S1097-2765(02)00459-8
J. R. Friedman, K. H. Kaestner, The Foxa family of transcription factors in development and metabolism Cellular and Molecular Life Sciences. ,vol. 63, pp. 2317- 2328 ,(2006) , 10.1007/S00018-006-6095-6
Cecilia S. L. Lai, Simon E. Fisher, Jane A. Hurst, Faraneh Vargha-Khadem, Anthony P. Monaco, A forkhead-domain gene is mutated in a severe speech and language disorder Nature. ,vol. 413, pp. 519- 523 ,(2001) , 10.1038/35097076
D N Gross, A P J van den Heuvel, M J Birnbaum, The Role of FoxO in the Regulation of Metabolism Oncogene. ,vol. 27, pp. 2320- 2336 ,(2008) , 10.1038/ONC.2008.25
D R Calnan, A Brunet, The FoxO code Oncogene. ,vol. 27, pp. 2276- 2288 ,(2008) , 10.1038/ONC.2008.21
Helen Berman, Kim Henrick, Haruki Nakamura, Announcing the worldwide Protein Data Bank Nature Structural & Molecular Biology. ,vol. 10, pp. 980- 980 ,(2003) , 10.1038/NSB1203-980
Kirk L. Clark, Elaine D Halay, Eseng Lai, Stephen K Burley, Co-crystal structure of the HNF-3/ fork head DNA-recognition motif resembles histone H5 Nature. ,vol. 364, pp. 412- 420 ,(1993) , 10.1038/364412A0
Makoto Miyara, Kajsa Wing, Shimon Sakaguchi, Therapeutic approaches to allergy and autoimmunity based on FoxP3+ regulatory T-cell activation and expansion. The Journal of Allergy and Clinical Immunology. ,vol. 123, pp. 749- 755 ,(2009) , 10.1016/J.JACI.2009.03.001