4.1 Article

Both Hoxc13 orthologs are functionally important for zebrafish tail fin regeneration

Journal

DEVELOPMENT GENES AND EVOLUTION
Volume 217, Issue 6, Pages 413-420

Publisher

SPRINGER
DOI: 10.1007/s00427-007-0154-3

Keywords

Hox; regeneration; morpholino; electroporation; zebrafish

Funding

  1. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR047233, R01AR039189] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R21DK061373] Funding Source: NIH RePORTER
  3. NIAMS NIH HHS [AR39189, AR47233] Funding Source: Medline
  4. NIDDK NIH HHS [R21 DK061373, R21 DK061373-02, DK61373] Funding Source: Medline

Ask authors/readers for more resources

Hox genes are re-expressed during regeneration in many species. Given their important role in body plan development, it has been assumed, but not directly shown, that they play a functional role in regeneration. In this paper we show that morpholino-mediated knockdown of either Hoxc13a or Hoxc13b during the process of zebrafish tail fin regeneration results in a significant reduction of regenerative outgrowth. Furthermore, cellular proliferation within the blastema is directly affected in both knockdowns. Hence, similar to the demonstration of unique functions of multiple Hox genes during limb formation, both Hoxc13 orthologs have distinct functions in regeneration.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available