» Articles » PMID: 17668071

Changing Hydrozoan Bauplans by Silencing Hox-like Genes

Overview
Journal PLoS One
Date 2007 Aug 2
PMID 17668071
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Regulatory genes of the Antp class have been a major factor for the invention and radiation of animal bauplans. One of the most diverse animal phyla are the Cnidaria, which are close to the root of metazoan life and which often appear in two distinct generations and a remarkable variety of body forms. Hox-like genes have been known to be involved in axial patterning in the Cnidaria and have been suspected to play roles in the genetic control of many of the observed bauplan changes. Unfortunately RNAi mediated gene silencing studies have not been satisfactory for marine invertebrate organisms thus far. No direct evidence supporting Hox-like gene induced bauplan changes in cnidarians have been documented as of yet. Herein, we report a protocol for RNAi transfection of marine invertebrates and demonstrate that knock downs of Hox-like genes in Cnidaria create substantial bauplan alterations, including the formation of multiple oral poles ("heads") by Cnox-2 and Cnox-3 inhibition, deformation of the main body axis by Cnox-5 inhibition and duplication of tentacles by Cnox-1 inhibition. All phenotypes observed in the course of the RNAi studies were identical to those obtained by morpholino antisense oligo experiments and are reminiscent of macroevolutionary bauplan changes. The reported protocol will allow routine RNAi studies in marine invertebrates to be established.

Citing Articles

Gene Loss may have Shaped the Cnidarian and Bilaterian Hox and ParaHox Complement.

Steinworth B, Martindale M, Ryan J Genome Biol Evol. 2022; 15(1).

PMID: 36508343 PMC: 9825252. DOI: 10.1093/gbe/evac172.


Hox and Wnt pattern the primary body axis of an anthozoan cnidarian before gastrulation.

DuBuc T, Stephenson T, Rock A, Martindale M Nat Commun. 2018; 9(1):2007.

PMID: 29789526 PMC: 5964151. DOI: 10.1038/s41467-018-04184-x.


Interspecific Differential Expression Analysis of RNA-Seq Data Yields Insight into Life Cycle Variation in Hydractiniid Hydrozoans.

Sanders S, Cartwright P Genome Biol Evol. 2015; 7(8):2417-31.

PMID: 26251524 PMC: 4558869. DOI: 10.1093/gbe/evv153.


Novel matrix proteins of Pteria penguin pearl oyster shell nacre homologous to the jacalin-related β-prism fold lectins.

Naganuma T, Hoshino W, Shikanai Y, Sato R, Liu K, Sato S PLoS One. 2014; 9(11):e112326.

PMID: 25375177 PMC: 4223035. DOI: 10.1371/journal.pone.0112326.


Molecular insights into the origin of the Hox-TALE patterning system.

Hudry B, Thomas-Chollier M, Volovik Y, Duffraisse M, Dard A, Frank D Elife. 2014; 3:e01939.

PMID: 24642410 PMC: 3957477. DOI: 10.7554/eLife.01939.


References
1.
Cartwright P, Bowsher J, Buss L . Expression of a Hox gene, Cnox-2, and the division of labor in a colonial hydroid. Proc Natl Acad Sci U S A. 1999; 96(5):2183-6. PMC: 26757. DOI: 10.1073/pnas.96.5.2183. View

2.
Cartwright P, Buss L . Colony integration and the expression of the Hox gene, Cnox-2, in Hydractinia symbiolongicarpus (Cnidaria: Hydrozoa). J Exp Zool. 1999; 285(1):57-62. DOI: 10.1002/(sici)1097-010x(19990415)285:1<57::aid-jez7>3.0.co;2-p. View

3.
Lohmann J, Endl I, Bosch T . Silencing of developmental genes in Hydra. Dev Biol. 1999; 214(1):211-4. DOI: 10.1006/dbio.1999.9407. View

4.
Li Y, Farrell M, Liu R, Mohanty N, Kirby M . Double-stranded RNA injection produces null phenotypes in zebrafish. Dev Biol. 2000; 217(2):394-405. DOI: 10.1006/dbio.1999.9540. View

5.
Gauchat D, Mazet F, Berney C, Schummer M, Kreger S, Pawlowski J . Evolution of Antp-class genes and differential expression of Hydra Hox/paraHox genes in anterior patterning. Proc Natl Acad Sci U S A. 2000; 97(9):4493-8. PMC: 18262. DOI: 10.1073/pnas.97.9.4493. View