This is a preview of subscription content, log in via an institution to check access.
References
Accili D. and Arden K. C. 2004 FoxOs at the crossroads of cellular metabolism, differentiation, and transformation. Cell 117, 421–426.
Barthel A., Schmoll D. and Unterman T. G. 2005 FoxO proteins in insulin action and metabolism. Trends Endocrinol. Metab. 16, 183–189.
Biggs Iii W. H., Meisenhelder J., Hunter T., Cavenee W. K. and Arden K. C. 1999 Protein kinase B / Akt - mediated phosphorylation promotes nuclear exclusion of the winged helix transcription factor FKHR1. Proc. Natl. Acad. Sci. USA 96, 7421–7426.
Boura E., Silhan J., Herman P., Vecer J., Sulc M., Teisinger J. et al. 2007 Both the N - terminal loop and wing W2 of the forkhead domain of transcription factor Foxo4 are important for DNA binding. J. Biol. Chem. 282, 8265–8275.
Burgering B. M. and Medema R. H. 2003 Decisions on life and death: FOXO forkhead transcription factors are in command when PKB/Akt is off duty. J. Leukoc. Biol. 73, 689–701.
Clark K. L., Halay E. D., Lai E. and Burley S. K. 1993 Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5. Nature 364, 412–420.
Fredericks W. J., Galili N., Mukhopadhyay S., Rovera G., Bennicelli J., Barr F. G. and Rauscher F. J. 1995 The PAX3-FKHR fusion protein created by the t (2; 13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3. Mol. Cell Biol. 15, 1522–1535.
Furuyama T., Nakazawa T., Nakano I. and Mori N. 2000 Identification of the differential distribution patterns of mRNAs and consensus binding sequences for mouse DAF-16 homologues. Biochem. J. 349, 629–634.
Gilley J., Coffer P. J. and Ham J. 2003 FOXO transcription factors directly activate bim gene expression and promote apoptosis in sympathetic neurons. J. Cell. Biol. 162, 613–622.
Greer E. L. and Brunet A. 2005 FOXO transcription factors at the interface between longevity and tumor suppression. Oncogene 24, 7410–7425.
Hribal M. L., Nakae J., Kitamura T., Shutter J. R. and Accili D. 2003 Regulation of insulin-like growth factor-dependent myoblast differentiation by Foxo forkhead transcription factors. J. Cell Biol. 162, 535–541.
Kaestner K. H., Knochel W. and Martinez D. E. 2000 Unified nomenclature for the winged helix/forkhead transcription factors. Genes Dev. 14, 142–146.
Kamei Y., Miura S., Suzuki M., Kai Y., Mizukami J., Taniguchi T. et al. 2004 Skeletal muscle FOXO1 (FKHR) transgenic mice have less skeletal muscle mass, down-regulated type I (slow twitch/red muscle) fiber genes, and impaired glycemic control. Biol. Chem. 279, 41114–41123.
Kyo S., Sakaguchi J., Kiyono T., Shimizu Y., Maida Y., Mizumoto Y. et al. 2011 Forkhead transcription factor FOXO1 is a direct target of progestin to inhibit endometrial epithelial cell growth. Clin. Cancer Res. 17, 525.
Mei Y., Wang Z., Zhang L., Zhang Y., Li X., Liu H. et al. 2012 Regulation of neuroblastoma differentiation by forkhead transcription factors FOXO1/3/4 through the receptor tyrosine kinase PDGFRA. Proc. Natl. Acad. Sci. USA 109, 4898– 4903.
Nakae J., Kitamura T., Kitamura Y., Biggs W. H. 3rd, Arden K. C. and Accili D. 2003 The forkhead transcription factor Foxo1 regulates adipocyte differentiation. Dev. Cell 4, 119–129.
Posada D. and Crandall K. A. 2001 Intraspecific gene genealogies: trees grafting into networks. Trends Ecol. Evol. 16, 37–45.
Sambrook J. and Russell D. W. 2001 Molecular cloning: a laboratory manual, vol. 3, 3rd edition. Cold Spring Harbor Laboratory Press, New York, USA.
Shi Y. Y. and He L. 2005 SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Cell Res. 15, 97–98.
Teixeira C. C., Liu Y. X., Thant L. M., Pang J., Palmer G. and Alikhani M. 2010 Foxo1, a novel regulator of osteoblast differentiation and skeletogenesis. J. Biol. Chem. 285, 31055–31065.
Tothova Z., Kollipara R., Huntly B. J., Lee B. H., Castrillon D. H., Cullen D. E. et al. 2007 FoxOs are critical mediators of hematopoietic stem cell resistance to physiologic oxidative stress. Cell 2, 325–339.
Tran H., Brunet A., Griffith E. C. and Greenberg M. E. 2003 The many forks in FOXO’s road. Sci. STKE. RE5.
Weigel D., Jurgens G., Kuttner F., Seifert E. and Jackle H. 1989 The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo. Cell 57, 645–658.
Acknowledgements
This study was supported by the National Natural Science Foundation of China (grant no. 30972080 and 30901023), Agricultural Science and Technology Innovation Projects of Shaanxi province (no. 2012NKC01-13), Program of National Beef Cattle Industrial Technology System (CARS-38).
Author information
Authors and Affiliations
Additional information
Sun Y., Xue J., Guo W., Li M., Huang Y., Lan X., Lei C., Zhang C. and Chen H. 2013 Haplotypes of bovine FoxO1 gene sequence variants and association with growth traits in Qinchuan cattle. J. Genet. 92, e8–e14. Online only: http://www.ias.ac.in/jgenet/OnlineResources/92/e8.pdf
Rights and permissions
About this article
Cite this article
SUN, Y., XUE, J., GUO, W. et al. Haplotypes of bovine FoxO1 gene sequence variants and association with growth traits in Qinchuan cattle. J Genet 93 (Suppl 2), 8–14 (2016). https://doi.org/10.1007/s12041-013-0209-3
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12041-013-0209-3