TY - JOUR
T1 - Developmental biology
T2 - fgf20 is essential for initiating zebrafish fin regeneration
AU - Whitehead, Geoffrey G.
AU - Makino, Shinji
AU - Lien, Ching Ling
AU - Keating, Mark T.
PY - 2005/12/23
Y1 - 2005/12/23
N2 - Epimorphic regeneration requires the presence or creation of pluripotent cells capable of reproducing lost organs. Zebrafish fin regeneration is mediated by the creation of blastema cells. Here, we characterize the devoid of blastema (dob) mutant that fails fin regeneration during initial steps, forms abnormal regeneration epithelium, and does not form blastema. This mutation has no impact on embryonic survival. Dob results from an fgf20a null mutation, Y148S. Fgf20a is expressed during initiation of fin regeneration at the epithelial-mesenchymal boundary and later overlaps with the blastema marker msxb. Thus, fgf20a has a regeneration-specific requirement, initiating fin regeneration, and controlling blastema formation.
AB - Epimorphic regeneration requires the presence or creation of pluripotent cells capable of reproducing lost organs. Zebrafish fin regeneration is mediated by the creation of blastema cells. Here, we characterize the devoid of blastema (dob) mutant that fails fin regeneration during initial steps, forms abnormal regeneration epithelium, and does not form blastema. This mutation has no impact on embryonic survival. Dob results from an fgf20a null mutation, Y148S. Fgf20a is expressed during initiation of fin regeneration at the epithelial-mesenchymal boundary and later overlaps with the blastema marker msxb. Thus, fgf20a has a regeneration-specific requirement, initiating fin regeneration, and controlling blastema formation.
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UR - http://www.scopus.com/inward/citedby.url?scp=29344463583&partnerID=8YFLogxK
U2 - 10.1126/science.1117637
DO - 10.1126/science.1117637
M3 - Article
C2 - 16373575
AN - SCOPUS:29344463583
SN - 0036-8075
VL - 310
SP - 1957
EP - 1960
JO - Science
JF - Science
IS - 5756
ER -