Literature DB >> 12622731

Comparison of even-skipped related gene expression pattern in vertebrates shows an association between expression domain loss and modification of selective constraints on sequences.

Fabien Avaron1, Christelle Thaëron-Antono, Caroline W Beck, Véronique Borday-Birraux, Jacqueline Géraudie, Didier Casane, Patrick Laurenti.   

Abstract

The even-skipped related genes (evx) encode homeodomain-containing transcription factors that play key roles in body patterning and neurogenesis in a wide array of Eumetazoa species. It is thought that the genome of the last common ancestor of Chordata contained a unique evx gene linked to a unique ancestral Hox complex. During subsequent evolution, two rounds of whole genome duplication followed by individual gene losses gave rise to three paralogs: evx1, evx2, and eve1. Then, eve1 was maintained in Actinopterygii lineage but not in Tetrapoda. To explain this discrepancy, we examined the expression patterns of the evx1 homologue, Xhox3, in Xenopus laevis and that of evx1 and eve1 in Danio rerio. We show here that Xhox3 is expressed in a manner that closely reflects the inferred expression pattern of the evx1 gene in the last common ancestor of Vertebrata (i.e., in gastrula, the central nervous system, the posterior gut, and the tip of the growing tail). Zebrafish evx1 and Xenopus Xhox3 are expressed in homologous cell lineages of the central nervous system and of the posterior gut, but evx1 was undetectable in the gastrula and the tail bud. Strikingly, eve1 is the only evx gene of zebrafish to be expressed in these two latter regions. Thus, the ancestral expression pattern of evx1 in vertebrates appears to have been distributed between evx1 and eve1 in zebrafish. We propose that evx1 and eve1 underwent a complementary loss of expression domain in zebrafish that allowed the maintenance of the two paralogs in accordance with the duplication-degeneration-complementation model. It is important to note that, in zebrafish, Evx1 and Eve1 have lost most of the protein domain upstream of the homeodomain. In addition, Eve1 has accumulated substitutions in positions that are highly conserved in all other Evx proteins. Thus, the reduction of the expression domain of both evx1 and eve1 in zebrafish appears to be associated with the modification of constraints on the protein sequences, allowing the shortening of both genes and an accelerated substitution rate in eve1.

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Year:  2003        PMID: 12622731     DOI: 10.1046/j.1525-142x.2003.03021.x

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


  8 in total

1.  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

2.  Conserved deployment of genes during odontogenesis across osteichthyans.

Authors:  Gareth J Fraser; Anthony Graham; Moya M Smith
Journal:  Proc Biol Sci       Date:  2004-11-22       Impact factor: 5.349

3.  Even-Skipped(+) Interneurons Are Core Components of a Sensorimotor Circuit that Maintains Left-Right Symmetric Muscle Contraction Amplitude.

Authors:  Ellie S Heckscher; Aref Arzan Zarin; Serge Faumont; Matthew Q Clark; Laurina Manning; Akira Fushiki; Casey M Schneider-Mizell; Richard D Fetter; James W Truman; Maarten F Zwart; Matthias Landgraf; Albert Cardona; Shawn R Lockery; Chris Q Doe
Journal:  Neuron       Date:  2015-10-01       Impact factor: 17.173

4.  Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α.

Authors:  Huang-Wei Lien; Rey-Yue Yuan; Chih-Ming Chou; Yi-Chung Chen; Chin-Chun Hung; Chin-Hwa Hu; Sheng-Ping L Hwang; Pung-Pung Hwang; Chia-Ning Shen; Chih-Lung Chen; Chia-Hsiung Cheng; Chang-Jen Huang
Journal:  Sci Rep       Date:  2016-06-21       Impact factor: 4.379

5.  Lmx1b is required for the glutamatergic fates of a subset of spinal cord neurons.

Authors:  William C Hilinski; Jonathan R Bostrom; Samantha J England; José L Juárez-Morales; Sarah de Jager; Olivier Armant; Jessica Legradi; Uwe Strähle; Brian A Link; Katharine E Lewis
Journal:  Neural Dev       Date:  2016-08-23       Impact factor: 3.842

6.  Evx1 and Evx2 specify excitatory neurotransmitter fates and suppress inhibitory fates through a Pax2-independent mechanism.

Authors:  José L Juárez-Morales; Claus J Schulte; Sofia A Pezoa; Grace K Vallejo; William C Hilinski; Samantha J England; Sarah de Jager; Katharine E Lewis
Journal:  Neural Dev       Date:  2016-02-19       Impact factor: 3.842

7.  Heterogeneous conservation of Dlx paralog co-expression in jawed vertebrates.

Authors:  Mélanie Debiais-Thibaud; Cushla J Metcalfe; Jacob Pollack; Isabelle Germon; Marc Ekker; Michael Depew; Patrick Laurenti; Véronique Borday-Birraux; Didier Casane
Journal:  PLoS One       Date:  2013-06-28       Impact factor: 3.240

Review 8.  Intracellular Communication among Morphogen Signaling Pathways during Vertebrate Body Plan Formation.

Authors:  Kimiko Takebayashi-Suzuki; Atsushi Suzuki
Journal:  Genes (Basel)       Date:  2020-03-24       Impact factor: 4.096

  8 in total

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