Abstract

BackgroundThe homeobox genes Pdx and Cdx are widespread across the animal kingdom and part of the small ParaHox gene cluster. Gene expression patterns suggest ancient roles for Pdx and Cdx in patterning the through-gut of bilaterian animals although functional data are available for few lineages. To examine evolutionary conservation of Pdx and Cdx gene functions, we focus on amphioxus, small marine animals that occupy a pivotal position in chordate evolution and in which ParaHox gene clustering was first reported.ResultsUsing transcription activator-like effector nucleases (TALENs), we engineer frameshift mutations in the Pdx and Cdx genes of the amphioxus Branchiostoma floridae and establish mutant lines. Homozygous Pdx mutants have a defect in amphioxus endoderm, manifest as loss of a midgut region expressing endogenous GFP. The anus fails to open in homozygous Cdx mutants, which also have defects in posterior body extension and epidermal tail fin development. Treatment with an inverse agonist of retinoic acid (RA) signalling partially rescues the axial and tail fin phenotypes indicating they are caused by increased RA signalling. Gene expression analyses and luciferase assays suggest that posterior RA levels are kept low in wild type animals by a likely direct transcriptional regulation of a Cyp26 gene by Cdx. Transcriptome analysis reveals extensive gene expression changes in mutants, with a disproportionate effect of Pdx and Cdx on gut-enriched genes and a colinear-like effect of Cdx on Hox genes.ConclusionsThese data reveal that amphioxus Pdx and Cdx have roles in specifying middle and posterior cell fates in the endoderm of the gut, roles that likely date to the origin of Bilateria. This conclusion is consistent with these two ParaHox genes playing a role in the origin of the bilaterian through-gut with a distinct anus, morphological innovations that contributed to ecological change in the Cambrian. In addition, we find that amphioxus Cdx promotes body axis extension through a molecular mechanism conserved with vertebrates. The axial extension role for Cdx dates back at least to the origin of Chordata and may have facilitated the evolution of the post-anal tail and active locomotion in chordates.

Highlights

  • The homeobox genes Pdx and Cdx are widespread across the animal kingdom and part of the small ParaHox gene cluster

  • Two transcription activator-like effector nucleases (TALENs) mRNAs were co-injected into unfertilised eggs of B. floridae and successful mutagenesis detected by PCR on pools of neurula stage embryos (Additional file 1: Table S1, Fig. S7)

  • Remaining embryos were reared to maturity to generate mosaic F0 animals; founders were spawned and mutations typed by PCR on sperm or pools of neurulae generated by outcrossing

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Summary

Introduction

The homeobox genes Pdx and Cdx are widespread across the animal kingdom and part of the small ParaHox gene cluster. The discovery that three homeobox genes, Gsx, Pdx and Cdx, are organised in a small gene cluster raised the possibility that these genes might act in a coordinated way. This ParaHox cluster was first described in the amphioxus Branchiostoma floridae [1], and later in human, several other vertebrates, an echinoderm, a hemichordate and two molluscs [2,3,4,5,6,7,8]. Gsx is expressed primarily in neural tissue in amphioxus, Drosophila and mouse [1]

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