|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
1 Committee on Developmental Biology, The University of Chicago, 1027 E 57th Street, Chicago, IL 60637, USA
2 Department of Organismal Biology and Anatomy, The University of Chicago, 1027 E 57th Street, Chicago, IL 60637, USA
3 Committees on Neurobiology and Evolutionary Biology, The University of Chicago, 1027 E 57th Street, Chicago, IL 60637, USA
*Author for correspondence (e-mail: vprince{at}midway.uchicago.edu)
Accepted April 9, 2001
As a result of a whole genome duplication event in the lineage leading to teleosts, the zebrafish has seven clusters of Hox patterning genes, rather than four, as described for tetrapod vertebrates. To investigate the consequences of this genome duplication, we have carried out a detailed comparison of genes from a single Hox paralogue group, paralogue group (PG) 1. We have analyzed the sequences, expression patterns and potential functions of all four of the zebrafish PG1 Hox genes, and compared our data with that available for the three mouse genes. As the basic functions of Hox genes appear to be tightly constrained, comparison with mouse data has allowed us to identify specific changes in the developmental roles of Hox genes that have occurred during vertebrate evolution. We have found variation in expression patterns, amino acid sequences within functional domains, and potential gene functions both within the PG1 genes of zebrafish, and in comparison to mouse PG1 genes. We observed novel expression patterns in the midbrain, such that zebrafish hoxa1a and hoxc1a are expressed anterior to the domain traditionally thought to be under Hox patterning control. The hoxc1a gene shows significant coding sequence changes in known functional domains, which correlate with a reduced capacity to cause posteriorizing transformations. Moreover, the hoxb1 duplicate genes have differing functional capacities, suggesting divergence after duplication. We also find that an intriguing function shuffling between paralogues has occurred, such that one of the zebrafish hoxb1 duplicates, hoxb1b, performs the role in hindbrain patterning played in mouse by the non-orthologous Hoxa1 gene.
Key words: Hox, Vertebrate, Zebrafish, Gene duplication, Hindbrain, Midbrain, Mauthner neurone, MLF
This article has been cited by other articles:
![]() |
K. Laue, S. Daujat, J. G. Crump, N. Plaster, H. H. Roehl, Tubingen 2000 Screen Consortium, C. B. Kimmel, R. Schneider, and M. Hammerschmidt The multidomain protein Brpf1 binds histones and is required for Hox gene expression and segmental identity Development, June 1, 2008; 135(11): 1935 - 1946. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Gitelman Evolution of the vertebrate twist family and synfunctionalization: a mechanism for differential gene loss through merging of expression domains Mol. Biol. Evol., September 1, 2007; 24(9): 1912 - 1925. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Nishikawa, A. A. Biewener, P. Aerts, A. N. Ahn, H. J. Chiel, M. A. Daley, T. L. Daniel, R. J. Full, M. E. Hale, T. L. Hedrick, et al. Neuromechanics: an integrative approach for understanding motor control Integr. Comp. Biol., July 1, 2007; 47(1): 16 - 54. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Shimizu, Y.-K. Bae, and M. Hibi Cdx-Hox code controls competence for responding to Fgfs and retinoic acid in zebrafish neural tissue Development, December 1, 2006; 133(23): 4709 - 4719. [Abstract] [Full Text] [PDF] |
||||
![]() |
I M McGonnell and R C Fowkes Fishing for gene function - endocrine modelling in the zebrafish. J. Endocrinol., June 1, 2006; 189(3): 425 - 439. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Lecaudey, I. Anselme, F. Rosa, and S. Schneider-Maunoury The zebrafish Iroquois gene iro7 positions the r4/r5 boundary and controls neurogenesis in the rostral hindbrain Development, July 1, 2004; 131(13): 3121 - 3131. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. T. Miller, L. Maves, and C. B. Kimmel moz regulates Hox expression and pharyngeal segmental identity in zebrafish Development, May 15, 2004; 131(10): 2443 - 2461. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Hale, M. A. Kheirbek, J. E. Schriefer, and V. E. Prince Hox Gene Misexpression and Cell-Specific Lesions Reveal Functionality of Homeotically Transformed Neurons J. Neurosci., March 24, 2004; 24(12): 3070 - 3076. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Murakami, M. Pasqualetti, Y. Takio, S. Hirano, F. M. Rijli, and S. Kuratani Segmental development of reticulospinal and branchiomotor neurons in lamprey: insights into the evolution of the vertebrate hindbrain Development, March 1, 2004; 131(5): 983 - 995. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Deflorian, N. Tiso, E. Ferretti, D. Meyer, F. Blasi, M. Bortolussi, and F. Argenton Prep1.1 has essential genetic functions in hindbrain development and cranial neural crest cell differentiation Development, February 1, 2004; 131(3): 613 - 627. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Amores, T. Suzuki, Y.-L. Yan, J. Pomeroy, A. Singer, C. Amemiya, and J. H. Postlethwait Developmental Roles of Pufferfish Hox Clusters and Genome Evolution in Ray-Fin Fish Genome Res., January 1, 2004; 14(1): 1 - 10. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Grandel, K. Lun, G.-J. Rauch, M. Rhinn, T. Piotrowski, C. Houart, P. Sordino, A. M. Kuchler, S. Schulte-Merker, R. Geisler, et al. Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin bud Development, March 8, 2003; 129(12): 2851 - 2865. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Itoh, T. Kudoh, M. Dedekian, C.-H. Kim, and A. B. Chitnis A role for iro1 and iro7 in the establishment of an anteroposterior compartment of the ectoderm adjacent to the midbrain-hindbrain boundary Development, March 7, 2003; 129(10): 2317 - 2327. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. McClintock, M. A. Kheirbek, and V. E. Prince Knockdown of duplicated zebrafish hoxb1 genes reveals distinct roles in hindbrain patterning and a novel mechanism of duplicate gene retention Development, March 7, 2003; 129(10): 2339 - 2354. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. G. L. Koh, K. Lam, A. Christoffels, M. V. Erdmann, S. Brenner, and B. Venkatesh Hox gene clusters in the Indonesian coelacanth, Latimeriamenadoensis PNAS, February 4, 2003; 100(3): 1084 - 1088. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. C. Yelick and T. F. Schilling MOLECULAR DISSECTION OF CRANIOFACIAL DEVELOPMENT USING ZEBRAFISH Crit. Rev. Oral. Biol. Med., July 1, 2002; 13(4): 308 - 322. [Abstract] [Full Text] |
||||
![]() |
C.-K. J. Shen Sharing Duties in the Family Genome Res., October 1, 2001; 11(10): 1615 - 1615. [Full Text] [PDF] |
||||