Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos

Developmental Dynamics

Volumn 240, Issue 8, 2011, Pages 1958-1963

  Canning, Claire A ^a   Chan, Jessica Sze Ki ^a   Common, John E A ^a   Lane, E Birgitte ^a   Jones, C Michael ^a  

^a INSTITUTE OF MEDICAL BIOLOGY   (Singapore)

Author keywords

Fermitin; Kindler syndrome; Kindlin; Xenopus

Indexed keywords

FERMITIN 1 PROTEIN; FERMITIN 2 PROTEIN; FERMITIN 3 PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; BONE MARROW CELL; CENTRAL NERVOUS SYSTEM; EAR; EMBRYO; GENE EXPRESSION; HEART; HEMATOPOIETIC CELL; MULTIGENE FAMILY; MUSCLE; NEURAL CREST; NONHUMAN; NOTOCHORD; OLFACTORY EPITHELIUM; ORTHOLOGY; PHARYNX; PRIORITY JOURNAL; SKIN; SOMITE; XENOPUS LAEVIS; YOLK SAC;

ANIMALS; EMBRYO, NONMAMMALIAN; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; MEMBRANE PROTEINS; NEOPLASM PROTEINS; PROTEIN ISOFORMS; TISSUE DISTRIBUTION; XENOPUS LAEVIS; XENOPUS PROTEINS;

XENOPUS LAEVIS;

EID: 79960364307     PISSN: 10588388     EISSN: 10970177     Source Type: Journal    
DOI: 10.1002/dvdy.22683     Document Type: Article

References (21)

1. Akazawa H, Kudoh S, Mochizuki N, Takekoshi N, Takano H, Nagai T, Komuro I. 2004. A novel LIM protein Cal promotes cardiac differentiation by association with CSX/NKX2-5. J Cell Biol 164: 395-405.
2. Ciau-Uitz A, Walmsley M, Patient R. 2000. Distinct origins of adult and embryonic blood in Xenopus. Cell 102: 787-796.
3. Costa RM, Soto X, Chen Y, Zorn AM, Amaya E. 2008. spib is required for primitive myeloid development in Xenopus. Blood 112: 2287-2296.
4. Harburger DS, Bouaouina M, Calderwood DA. 2009. Kindlin-1 and -2 directly bind the C-terminal region of beta integrin cytoplasmic tails and exert integrin-specific activation effects. J Biol Chem 284: 11485-11497.
5. Jobard F, Bouadjar B, Caux F, Hadj-Rabia S, Has C, Matsuda F, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J. 2003. Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. Hum Mol Genet 12: 925-935.
6. Jones CM, Smith JC. 2008. Mesoderm induction assays. Methods Mol Biol 461: 395-404.
7. Kindler T. 1954. Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy. Br J Dermatol 66: 104-111.
8. Kloeker S, Major MB, Calderwood DA, Ginsberg MH, Jones DA, Beckerle MC. 2004. The Kindler syndrome protein is regulated by transforming growth factor-beta and involved in integrin-mediated adhesion. J Biol Chem 279: 6824-6833.
9. Lane MC, Smith WC. 1999. The origins of primitive blood in Xenopus: implications for axial patterning. Development 126: 423-434.
10. Larjava H, Plow EF, Wu C. 2008. Kindlins: essential regulators of integrin signalling and cell-matrix adhesion. EMBO Rep 9: 1203-1208.
11. Lotem M, Raben M, Zeltser R, Landau M, Sela M, Wygoda M, Tochner ZA. 2001. Kindler syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor. Br J Dermatol 144: 1284-1286.
12. Malinin NL, Plow EF, Byzova TV. 2010. Kindlins in FERM adhesion. Blood 115: 4011-4017.
13. Moser M, Nieswandt B, Ussar S, Pozgajova M, Fassler R. 2008. Kindlin-3 is essential for integrin activation and platelet aggregation. Nat Med 14: 325-330.
14. Park BY, Saint-Jeannet JP. 2010. Expression analysis of Runx3 and other Runx family members during Xenopus development. Gene Expr Patterns 10: 159-166.
15. Pearson MA, Reczek D, Bretscher A, Karplus PA. 2000. Structure of the ERM protein moesin reveals the FERM domain fold masked by an extended actin binding tail domain. Cell 101: 259-270.
16. Sharma RC, Mahajan V, Sharma NL, Sharma AK. 2003. Kindler syndrome. Int J Dermatol 42: 727-732.
17. Siegel DH, Ashton GH, Penagos HG, Lee JV, Feiler HS, Wilhelmsen KC, South AP, Smith FJ, Prescott AR, Wessagowit V, Oyama N, Akiyama M, Al Aboud D, Al Aboud K, Al Githami A, Al Hawsawi K, Al Ismaily A, Al-Suwaid R, Atherton DJ, Caputo R, Fine JD, Frieden IJ, Fuchs E, Haber RM, Harada T, Kitajima Y, Mallory SB, Ogawa H, Sahin S, Shimizu H, Suga Y, Tadini G, Tsuchiya K, Wiebe CB, Wojnarowska F, Zaghloul AB, Hamada T, Mallipeddi R, Eady RA, McLean WH, McGrath JA, Epstein EH. 2003. Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet 73: 174-187.
18. Snider P, Olaopa M, Firulli AB, Conway SJ. 2007. Cardiovascular development and the colonizing cardiac neural crest lineage. Sci World J 7: 1090-1113.
19. Tepass U. 2009. FERM proteins in animal morphogenesis. Curr Opin Genet Dev 19: 357-367.
20. Ussar S, Moser M, Widmaier M, Rognoni E, Harrer C, Genzel-Boroviczeny O, Fassler R. 2008. Loss of Kindlin-1 causes skin atrophy and lethal neonatal intestinal epithelial dysfunction. PLoS Genet 4: e1000289.
21. Ussar S, Wang HV, Linder S, Fassler R, Moser M. 2006. The Kindlins: subcellular localization and expression during murine development. Exp Cell Res 312: 3142-3151.