Agr genes, missing in amniotes, are involved in the body appendages regeneration in frog tadpoles

Scientific Reports

Volumn 3, Issue , 2013, Pages

  Ivanova, Anastasiya S ^a   Tereshina, Maria B ^a   Ermakova, Galina V ^a   Belousov, Vsevolod V ^a   Zaraisky, Andrey G ^a  

^a SHEMYAKIN OVCHINNIKOV INSTITUTE OF BIOORGANIC CHEMISTRY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN DISULFIDE ISOMERASE; XAG 2 PROTEIN, XENOPUS; XAG-2 PROTEIN, XENOPUS; XENOPUS PROTEIN;

ANIMAL; ARTICLE; GENE; GENETICS; HINDLIMB; LARVA; PHYLOGENY; PHYSIOLOGY; REGENERATION; XENOPUS LAEVIS;

ANIMALS; GENES; HINDLIMB; LARVA; PHYLOGENY; PROTEIN DISULFIDE-ISOMERASES; REGENERATION; XENOPUS LAEVIS; XENOPUS PROTEINS;

MLCS; MLOWN;

EID: 84874299314     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep01279     Document Type: Article

References (19)

1. Sive, H. L., Hattori, K. & Weintraub, H. Progressive determination during formation of the anteroposterior axis in Xenopus laevis. Cell 58, 171-180 (1989).
2. Novoselov, V. V., Alexandrova, E. M., Ermakova, G. V. & Zaraisky, A. G. Expression zones of three novel genes abut the developing anterior neural plate of Xenopus embryo. Gene Expr Patterns 3, 225-230 (2003).
3. Persson, S. et al. Diversity of the protein disulfide isomerase family: identification of breast tumor induced Hag2 and Hag3 as novel members of the protein family. Molecular phylogenetics and evolution 36, 734-740 (2005).
4. Aberger, F., Weidinger, G., Grunz, H. & Richter, K. Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2. Mechanisms of development 72, 115-130 (1998).
5. Gray, T. A. et al. Anterior Gradient-3: a novel biomarker for ovarian cancer that mediates cisplatin resistance in xenograft models. Journal of immunological methods 378, 20-32 (2012).
6. Liu, D., Rudland, P. S., Sibson, D. R., Platt-Higgins, A. & Barraclough, R. Human homologue of cement gland protein, a novel metastasis inducer associated with breast carcinomas. Cancer research 65, 3796-3805 (2005).
7. Kumar, A., Godwin, J. W., Gates, P. B., Garza-Garcia, A. A. & Brockes, J. P. Molecular basis for the nerve dependence of limb regeneration in an adult vertebrate. Science New York, N.Y 318, 772-777 (2007).
8. Kumar, A. et al. The aneurogenic limb identifies developmental cell interactions underlying vertebrate limb regeneration. Proceedings of the National Academy of Sciences of the United States of America 108, 13588-13593 (2011).
9. Blassberg, R. A., Garza-Garcia, A., Janmohamed, A., Gates, P. B. & Brockes, J. P. Functional convergence of signalling by GPI-anchored and anchorless forms of a salamander protein implicated in limb regeneration. Journal of cell science 124, 47-56 (2011).
10. Slack, J.M., Lin, G. & Chen, Y. The Xenopus tadpole: a new model for regeneration research. Cell Mol Life Sci 65, 54-63 (2008).
11. Beck, C. W., Izpisua Belmonte, J. C. & Christen, B. Beyond early development: Xenopus as an emerging model for the study of regenerative mechanisms. Dev Dyn 238, 1226-1248 (2009).
12. Serebrovskaya, E. O. et al. Light-induced blockage of cell division with a chromatin-targeted phototoxic fluorescent protein. The Biochemical journal 435, 65-71 (2011).
13. Tschumi, P. A. The growth of the hindlimb bud of Xenopus laevis and its dependence upon the epidermis. Journal of anatomy 91, 149-173 (1957).
14. Nieuwkoop, P. D. & Faber, J. Normal table of Xenopus laevis (Daudin). (North-Holland Publ., Co., Amsterdam; 1956).
15. Bookout, A. L., Cummins, C. L., Mangelsdorf, D. J., Pesola, J. M. & Kramer, M. F. High-throughput real-time quantitative reverse transcription PCR. Current protocols in molecular biology 73, 15.18.11-15.18.28 (2006).
16. Xanthos, J. B. et al. The roles of three signaling pathways in the formation and function of the Spemann Organizer. Development (Cambridge, England) 129, 4027-4043 (2002).
17. Harland, R. M. In situ hybridization: an improved whole-mount method for Xenopus embryos. Methods in cell biology 36, 685-695 (1991).
18. Offield, M. F., Hirsch, N. & Grainger, R. M. The development of Xenopus tropicalis transgenic lines and their use in studying lens developmental timing in living embryos. Development (Cambridge, England) 127, 1789-1797 (2000).
19. Martynova, N. et al. Patterning the forebrain: FoxA4a/Pintallavis and Xvent2 determine the posterior limit of Xanf1 expression in the neural plate. Development (Cambridge, England) 131, 2329-2338 (2004).