spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online November 24, 2004
doi: 10.1242/10.1242/dev.01540


Development 131, 6225-6235 (2004)
Published by The Company of Biologists 2004


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in Development
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wingert, R. A.
Right arrow Articles by Zon, L. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wingert, R. A.
Right arrow Articles by Zon, L. I.
Right arrowPubmed/NCBI databases
*Domain*Gene
*HomoloGene*Protein
*UniGene
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*IRON
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

The chianti zebrafish mutant provides a model for erythroid-specific disruption of transferrin receptor 1

Rebecca A. Wingert, Alison Brownlie, Jenna L. Galloway, Kimberly Dooley, Paula Fraenkel, Jennifer L. Axe, Alan J. Davidson*, Bruce Barut, Laura Noriega, Xiaoming Sheng, Yi Zhou Tübingen 2000 Screen Consortium{dagger} and Leonard I. Zon*,{ddagger}

Department of Hematology/Oncology, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA

{ddagger} Author for correspondence (e-mail: zon{at}enders.tch.harvard.edu)

Accepted 20 October 2004

Iron is a crucial metal for normal development, being required for the production of heme, which is incorporated into cytochromes and hemoglobin. The zebrafish chianti (cia) mutant manifests a hypochromic, microcytic anemia after the onset of embryonic circulation, indicative of a perturbation in red blood cell hemoglobin production. We show that cia encodes tfr1a, which is specifically expressed in the developing blood and requisite only for iron uptake in erythroid precursors. In the process of isolating zebrafish tfr1, we discovered two tfr1-like genes (tfr1a and tfr1b) and a single tfr2 ortholog. Abrogation of tfr1b function using antisense morpholinos revealed that this paralog was dispensable for hemoglobin production in red cells. tfr1b morphants exhibited growth retardation and brain necrosis, similar to the central nervous system defects observed in the Tfr1 null mouse, indicating that tfr1b is probably used by non-erythroid tissues for iron acquisition. Overexpression of mouse Tfr1, mouse Tfr2, and zebrafish tfr1b partially rescued hypochromia in cia embryos, establishing that each of these transferrin receptors are capable of supporting iron uptake for hemoglobin production in vivo. Taken together, these data show that zebrafish tfr1a and tfr1b share biochemical function but have restricted domains of tissue expression, and establish a genetic model to study the specific function of Tfr1 in erythroid cells.

Key words: Zebrafish, Hematopoiesis, Transferrin receptor, Iron, Gene duplication


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?

Related articles in Development:

Ironing out iron uptake in zebrafish

Development 2004 131: e2406. [Full Text]  

Ironing out iron uptake in zebrafish

Development 2004 131: e2406. [Full Text]  



This article has been cited by other articles:


Home page
BloodHome page
P. G. Fraenkel, Y. Gibert, J. L. Holzheimer, V. J. Lattanzi, S. F. Burnett, K. A. Dooley, R. A. Wingert, and L. I. Zon
Transferrin-a modulates hepcidin expression in zebrafish embryos
Blood, March 19, 2009; 113(12): 2843 - 2850.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
A. L. Lumsden, T. L. Henshall, S. Dayan, M. T. Lardelli, and R. I. Richards
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development
Hum. Mol. Genet., August 15, 2007; 16(16): 1905 - 1920.
[Abstract] [Full Text] [PDF]


Home page
PhysiologyHome page
A. Donovan, C. N. Roy, and N. C. Andrews
The Ins and Outs of Iron Homeostasis
Physiology, April 1, 2006; 21(2): 115 - 123.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
G. E. Montanez, M. N. Neely, and Z. Eichenbaum
The streptococcal iron uptake (Siu) transporter is required for iron uptake and virulence in a zebrafish infection model
Microbiology, November 1, 2005; 151(11): 3749 - 3757.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2004