Literature DB >> 11440248

Additional hox clusters in the zebrafish: divergent expression patterns belie equivalent activities of duplicate hoxB5 genes.

A E Bruce1, A C Oates, V E Prince, R K Ho.   

Abstract

The evolution of metazoan body plans has involved changes to the Hox genes, which are involved in patterning the body axis and display striking evolutionary conservation of structure and expression. Invertebrates contain a single Hox cluster whereas tetrapods possess four clusters. The zebrafish has seven unlinked hox clusters, a finding that is difficult to reconcile with the notion that genomic complexity, reflected by Hox cluster number, and morphological complexity are causally linked, as the body plan of the zebrafish is not obviously more complex than that of the mouse or human. Why have the additional hox genes in zebrafish been conserved? To address the role of these additional zebrafish hox genes, we have examined the duplicate hoxB5 genes, hoxB5a, and hoxB5b. Conservation of gene duplicates can occur when one gene acquires a new function (neofunctionalization), or when the ancestral function is divided between the two duplicates (subfunctionalization). hoxB5a and hoxB5b are expressed in distinct domains, and their combined expression domain is strikingly similar to that of single Hoxb5 genes in other species. The biochemical functions encoded by the two genes were studied by overexpression, which resulted in identical developmental defects in the anterior hindbrain and cranial neural crest, suggesting strongly that hoxB5a and hoxB5b have equivalent biochemical properties with respect to early development. From these studies, we conclude that conservation of hoxB5a and hoxB5b is likely the result of division of the ancestral Hoxb5 function between the two genes, without significant changes in biochemical activity. These results suggest a resolution to the conundrum of the extra hox genes and clusters in the zebrafish, since if any of the additional hox genes in the zebrafish are similarly subfunctionalized, they are unlikely to supply novel genetic functions. Thus, the morphological complexity potentially conferred by the majority of additional zebrafish hox clusters may not be substantially greater than that conferred by the four tetrapod clusters.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11440248     DOI: 10.1046/j.1525-142x.2001.003003127.x

Source DB:  PubMed          Journal:  Evol Dev        ISSN: 1520-541X            Impact factor:   1.930


  22 in total

Review 1.  The COXes of Danio: from mechanistic model to experimental therapeutics.

Authors:  Stephen M Prescott; H Joseph Yost
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-01       Impact factor: 11.205

2.  Hox cluster duplications and the opportunity for evolutionary novelties.

Authors:  Gunte P Wagner; Chris Amemiya; Frank Ruddle
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-24       Impact factor: 11.205

3.  Phylogenetic analysis of vertebrate fibrillar collagen locates the position of zebrafish alpha3(I) and suggests an evolutionary link between collagen alpha chains and hox clusters.

Authors:  Ghislaine Morvan-Dubois; Dominique Le Guellec; Robert Garrone; Louise Zylberberg; Laure Bonnaud
Journal:  J Mol Evol       Date:  2003-11       Impact factor: 2.395

4.  Duplicated Abd-B class genes in medaka hoxAa and hoxAb clusters exhibit differential expression patterns in pectoral fin buds.

Authors:  Naofumi Takamatsu; Gene Kurosawa; Masayoshi Takahashi; Ryouichi Inokuma; Minoru Tanaka; Akira Kanamori; Hiroshi Hori
Journal:  Dev Genes Evol       Date:  2007-02-27       Impact factor: 0.900

5.  A novel light damage paradigm for use in retinal regeneration studies in adult zebrafish.

Authors:  Jennifer L Thomas; Ryan Thummel
Journal:  J Vis Exp       Date:  2013-10-24       Impact factor: 1.355

Review 6.  The fates of zebrafish Hox gene duplicates.

Authors:  Chris Jozefowicz; James McClintock; Victoria Prince
Journal:  J Struct Funct Genomics       Date:  2003

7.  Duplicate dmbx1 genes regulate progenitor cell cycle and differentiation during zebrafish midbrain and retinal development.

Authors:  Loksum Wong; Cameron J Weadick; Claire Kuo; Belinda S W Chang; Vincent Tropepe
Journal:  BMC Dev Biol       Date:  2010-09-22       Impact factor: 1.978

8.  Increased Hox activity mimics the teratogenic effects of excess retinoic acid signaling.

Authors:  Joshua S Waxman; Deborah Yelon
Journal:  Dev Dyn       Date:  2009-05       Impact factor: 3.780

9.  Hoxb5b acts downstream of retinoic acid signaling in the forelimb field to restrict heart field potential in zebrafish.

Authors:  Joshua S Waxman; Brian R Keegan; Richard W Roberts; Kenneth D Poss; Deborah Yelon
Journal:  Dev Cell       Date:  2008-12       Impact factor: 12.270

10.  The fate of the duplicated androgen receptor in fishes: a late neofunctionalization event?

Authors:  Véronique Douard; Frédéric Brunet; Bastien Boussau; Isabelle Ahrens-Fath; Virginie Vlaeminck-Guillem; Bernard Haendler; Vincent Laudet; Yann Guiguen
Journal:  BMC Evol Biol       Date:  2008-12-18       Impact factor: 3.260

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.