Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw

Development

Volumn 134, Issue 8, 2007, Pages 1605-1615

  Schottenfeld, Jodi ^a   Sullivan Brown, Jessica ^a   Burdine, Rebecca D ^a  

^a PRINCETON UNIVERSITY   (United States)

Author keywords

Asymmetry; Cilia; Kidney; Laterality; Left right axis; pkd2; Pronephros; Zebrafish

Indexed keywords

ANTISENSE OLIGONUCLEOTIDE; MORPHOLINE DERIVATIVE; POLYCYSTIN 2; PROTEIN NODAL;

ANIMAL TISSUE; ARTICLE; BRAIN ASYMMETRY; CALCIUM TRANSPORT; CONCENTRATION RESPONSE; CONTROLLED STUDY; DIENCEPHALON; EMBRYO; ENDODERM; GENE ACTIVATION; GENE EXPRESSION REGULATION; GENE MUTATION; GENETIC ANALYSIS; HETEROTAXY SYNDROME; MESODERM; MORPHOGENESIS; MOUSE; MUTANT; NONHUMAN; ORGANOGENESIS; ORTHOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; SPECIES COMPARISON; TRANSCRIPTION INITIATION; ZEBRA FISH;

ALLELES; ANIMALS; BODY PATTERNING; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MESODERM; MICE; MUTATION; TRANSFORMING GROWTH FACTOR BETA; TRPP CATION CHANNELS; ZEBRAFISH; ZEBRAFISH PROTEINS;

DANIO RERIO;

EID: 34248597580     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.02827     Document Type: Article

References (57)

1. Ahmad, N., Long, S. and Rebagliati, M. (2004). A southpaw joins the roster: the role of the zebrafish nodal-related gene southpaw in cardiac LR asymmetry. Trends Cardiovasc. Med. 14, 43-49.
2. Alexander, J. and Stainier, D. Y. (1999). A molecular pathway leading to endoderm formation in zebrafish. Curr. Biol. 9, 1147-1157.
3. Amack, J. D. and Yost, H. J. (2004). The T box transcription factor no tail in ciliated cells controls zebrafish left-right asymmetry. Curr. Biol. 14, 685-690.
4. Bisgrove, B. W., Essner, J. J. and Yost, H. J. (1999). Regulation of midline development by antagonism of lefty and nodal signaling. Development 126, 3253-3262.
5. Bisgrove, B. W., Snarr, B. S., Emrazian, A. and Yost, H. J. (2005). Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis. Dev. Biol. 287, 274-288.
6. Boettger, T., Wittler, L. and Kessel, M. (1999). FGF8 functions in the specification of the right body side of the chick. Curr. Biol. 9, 277-280.
7. Brand, M., Heisenberg, C. P., Jiang, Y. J., Beuchle, D., Lun, K., Furutani-Seiki, M., Granato, M., Haffter, P., Hammerschmidt, M., Kane, D. A. et al. (1996). Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain. Development 123, 179-190.
8. Burdine, R. D. and Schier, A. F. (2000). Conserved and divergent mechanisms in left-right axis formation. Genes Dev. 14, 763-776.
9. Chen, J. N., van Eeden, F. J., Warren, K. S., Chin, A., Nusslein-Volhard, C., Haffter, P. and Fishman, M. C. (1997). Left-right pattern of cardiac BMP4 may drive asymmetry of the heart in zebrafish. Development 124, 4373-4382.
10. Cleaver, O. B., Patterson, K. D. and Krieg, P. A. (1996). Overexpression of the tinman-related genes XNkx-2.5 and XNkx-2.3 in Xenopus embryos results in myocardial hyperplasia. Development 122, 3549-3556.
11. Concha, M. L., Burdine, R. D., Russell, C., Schier, A. F. and Wilson, S. W. (2000). A nodal signaling pathway regulates the laterality of neuroanatomical asymmetries in the zebrafish forebrain. Neuron 28, 399-409.
12. Delmas, P., Padilla, F., Osorio, N., Coste, B., Raoux, M. and Crest, M. (2004). Polycystins, calcium signaling, and human diseases. Biochem. Biophys. Res. Commun. 322, 1374-1383.
13. Essner, J. J., Branford, W. W., Zhang, J. and Yost, H. J. (2000). Mesendoderm and left-right brain, heart and gut development are differentially regulated by pitx2 isoforms. Development 127, 1081-1093.
14. Essner, J. J., Vogan, K. J., Wagner, M. K., Tabin, C. J., Yost, H. J. and Brueckner, M. (2002). Conserved function for embryonic nodal cilia. Nature 418, 37-38.
15. Essner, J. J., Amack, J. D., Nyholm, M. K., Harris, E. B. and Yost, H. J. (2005). Kupffer's vesicle is a ciliated organ of asymmetry in the zebrafish embryo that initiates left-right development of the brain, heart and gut. Development 132, 1247-1260.
16. Fischer, A., Viebahn, C. and Blum, M. (2002). FGF8 acts as a right determinant during establishment of the left-right axis in the rabbit. Curr. Biol. 12, 1807-1816.
17. Gamse, J. T., Shen, Y. C., Thisse, C., Thisse, B., Raymond, P. A., Halpern, M. E. and Liang, J. O. (2002). Otx5 regulates genes that show circadian expression in the zebrafish pineal complex. Nat. Genet. 30, 117-121.
18. Gamse, J. T., Thisse, C., Thisse, B. and Halpern, M. E. (2003). The parapineal mediates left-right asymmetry in the zebrafish diencephalon. Development 130, 1059-1068.
19. Gonzalez-Perrett, S., Kim, K., Ibarra, C., Damiano, A. E., Zotta, E., Batelli, M., Harris, P. C., Reisin, I. L., Arnaout, M. A. and Cantiello, H. F. (2001). Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel. Proc. Natl. Acad. Sci. USA 98, 1182-1187.
20. Gritsman, K., Zhang, J., Cheng, S., Heckscher, E., Talbot, W. S. and Schier, A. F. (1999). The EGF-CFC protein one-eyed pinhead is essential for nodal signaling. Cell 97, 121-132.
21. Haffter, P., Granato, M., Brand, M., Mullins, M. C., Hammerschmidt, M., Kane, D. A., Odenthal, J., van Eeden, F. J., Jiang, Y. J., Heisenberg, C. P. et al. (1996). The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. Development 123, 1-36.
22. Hanaoka, K., Qian, F., Boletta, A., Bhunia, A. K., Piontek, K., Tsiokas, L., Sukhatme, V. P., Guggino, W. B. and Germino, G. G. (2000). Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents. Nature 408, 990-994.
23. Hashimoto, H., Rebagliati, M., Ahmad, N., Muraoka, O., Kurokawa, T., Hibi, M. and Suzuki, T. (2004). The Cerberus/Dan-family protein Charon is a negative regulator of Nodal signaling during left-right patterning in zebrafish. Development 131, 1741-1753.
24. Hayashi, T., Mochizuki, T., Reynolds, D. M., Wu, G., Cai, Y. and Somlo, S. (1997). Characterization of the exon structure of the polycystic kidney disease 2 gene (PKD2). Genomics 44, 131-136.
25. Kramer-Zucker, A. G., Olale, F., Haycraft, C. J., Yoder, B. K., Schier, A. F. and Drummond, I. A. (2005). Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis. Development 132, 1907-1921.
26. Krauss, S., Concordet, J. P. and Ingham, P. W. (1993). A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos. Cell 75, 1431-1444.
27. Liao, E. C. and Zon, L. I. (1999). Simple sequence-length polymorphism analysis. Methods Cell Biol. 60, 181-183.
28. Liu, S., Lu, W., Obara, T., Kuida, S., Lehoczky, J., Dewar, K., Drummond, I. A. and Beier, D. R. (2002). A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development 129, 5839-5846.
29. McGrath, J. and Brueckner, M. (2003). Cilia are at the heart of vertebrate left-right asymmetry. Curr. Opin. Genet. Dev. 13, 385-392.
30. McGrath, J., Somlo, S., Makova, S., Tian, X. and Brueckner, M. (2003). Two populations of node monocilia initiate left-right asymmetry in the mouse. Cell 114, 61-73.
31. Mercola, M. and Levin, M. (2001). Left-right asymmetry determination in vertebrates. Annu. Rev. Cell Dev. Biol. 17, 779-805.
32. Meyers, E. N. and Martin, G. R. (1999). Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science 285, 403-406.
33. Milewski, W. M., Duguay, S. J., Chan, S. J. and Steiner, D. F. (1998). Conservation of PDX-1 structure, function, and expression in zebrafish. Endocrinology 139, 1440-1449.
34. Nakamura, T., Mine, N., Nakaguchi, E., Mochizuki, A., Yamamoto, M., Yashiro, K., Meno, C. and Hamada, H. (2006). Generation of robust left-right asymmetry in the mouse embryo requires a self-enhancement and lateral-inhibition system. Dev. Cell 11, 495-504.
35. Nauli, S. M., Alenghat, F. J., Luo, Y., Williams, E., Vassilev, P., Li, X., Elia, A. E., Lu, W., Brown, E. M., Quinn, S. J. et al. (2003). Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells. Nat. Genet. 33, 129-137.
36. Odenthal, J. and Nusslein-Volhard, C. (1998). fork head domain genes in zebrafish. Dev. Genes Evol. 208, 245-258.
37. Ohara, O., Dorit, R. L. and Gilbert, W. (1989). One-sided polymerase chain reaction: the amplification of cDNA. Proc. Natl. Acad. Sci. USA 86, 5673-5677.
38. Okada, Y., Takeda, S., Tanaka, Y., Belmonte, J. C. and Hirokawa, N. (2005). Mechanism of nodal flow: a conserved symmetry breaking event in left-right axis determination. Cell 121, 633-644.
39. Otto, E. A., Schermer, B., Obara, T., O'Toole, J. F., Hiller, K. S., Mueller, A. M., Ruf, R. G., Hoefele, J., Beekmann, F., Landau, D. et al. (2003). Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. Nat. Genet. 34, 413-420.
40. Pennekamp, P., Karcher, C., Fischer, A., Schweickert, A., Skryabin, B., Horst, J., Blum, M. and Dworniczak, B. (2002). The ion channel polycystin-2 is required for left-right axis determination in mice. Curr. Biol. 12, 938-943.
41. Qiu, D., Cheng, S. M., Wozniak, L., McSweeney, M., Perrone, E. and Levin, M. (2005). Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left-right asymmetry. Dev. Dyn. 234, 176-189.
42. Ramsdell, A. F. (2005). Left-right asymmetry and congenital cardiac defects: getting to the heart of the matter in vertebrate left-right axis determination. Dev. Biol. 288, 1-20.
43. Raya, A., Kawakami, Y., Rodriguez-Esteban, C., Ibanes, M., Rasskin-Gutman, D., Rodriguez-Leon, J., Buscher, D., Feijo, J. A. and Izpisua Belmonte, J. C. (2004). Notch activity acts as a sensor for extracellular calcium during vertebrate left-right determination. Nature 427, 121-128.
44. Roessler, E. and Muenke, M. (2001). Midline and laterality defects: left and right meet in the middle. BioEssays 23, 888-900.
45. Sarmah, B., Latimer, A. J., Appel, B. and Wente, S. R. (2005). Inositol polyphosphates regulate zebrafish left-right asymmetry. Dev. Cell 9, 133-145.
46. Struhl, G. (1981). Anterior and posterior compartments in the proboscis of Drosophila. Dev. Biol. 84, 372-385.
47. Sun, Z. and Hopkins, N. (2001). vhnf1, the MODY5 and familial GCKD-associated gene, regulates regional specification of the zebrafish gut, pronephros, and hindbrain. Genes Dev. 15, 3217-3229.
48. Sun, Z., Amsterdam, A., Pazour, G. J., Cole, D. G., Miller, M. S. and Hopkins, N. (2004). A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney. Development 131, 4085-4093.
49. Tabin, C. J. and Vogan, K. J. (2003). A two-cilia model for vertebrate left-right axis specification. Genes Dev. 17, 1-6.
50. Talbot, W. S. and Schier, A. F. (1999). Positional cloning of mutated zebrafish genes. Methods Cell Biol. 60, 259-286.
51. Thisse, C. and Thisse, B. (1999). Antivin, a novel and divergent member of the TGFbeta superfamily, negatively regulates mesoderm induction. Development 126, 229-240.
52. Vassilev, P. M., Guo, L., Chen, X. Z., Segal, Y., Peng, J. B., Basora, N., Babakhanlou, H., Cruger, G., Kanazirska, M., Ye, C. et al. (2001). Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease. Biochem. Biophys. Res. Commun. 282, 341-350.
53. Webb, S. E. and Miller, A. L. (2000). Calcium signalling during zebrafish embryonic development. BioEssays 22, 113-123.
54. Wu, G., Mochizuki, T., Le, T. C., Cai, Y., Hayashi, T., Reynolds, D. M. and Somlo, S. (1997). Molecular cloning, cDNA sequence analysis, and chromosomal localization of mouse Pkd2. Genomics 45, 220-223.
55. Wu, G., Markowitz, G. S., Li, L., D'Agati, V. D., Factor, S. M., Geng, L., Tibara, S., Tuchman, J., Cai, Y., Park, J. H. et al. (2000). Cardiac defects and renal failure in mice with targeted mutations in Pkd2. Nat. Genet. 24, 75-78.
56. Yan, Y. T., Gritsman, K., Ding, J., Burdine, R. D., Corrales, J. D., Price, S. M., Talbot, W. S., Schier, A. F. and Shen, M. M. (1999). Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation. Genes Dev. 13, 2527-2537.
57. Yelon, D., Horne, S. A. and Stainier, D. Y. (1999). Restricted expression of cardiac myosin genes reveals regulated aspects of heart tube assembly in zebrafish. Dev. Biol. 214, 23-37.