PUBLICATION
Zebrafish ftz-f1a (nuclear receptor 5a2) functions in skeletal muscle organization
- Authors
- Sheela, S.G., Lee, W.C., Lin, W.W., and Chung, B.C.
- ID
- ZDB-PUB-050920-2
- Date
- 2005
- Source
- Developmental Biology 286(2): 377-390 (Journal)
- Registered Authors
- Chung, Bon-chu, Devakanmalai, Sheela Sundaram Gnanapackiam, Lee, Wen-Chih, Lin, Wen-Wen
- Keywords
- NR5A2, ff1a, LRH-1, FTF, Hedgehog, ubo, syu, yot, prox1, Twitch fiber
- MeSH Terms
-
- Animals
- Embryo, Nonmammalian
- Hedgehog Proteins
- Homeodomain Proteins/genetics
- Homeodomain Proteins/physiology*
- Morphogenesis*
- Muscle Fibers, Fast-Twitch
- Muscle Fibers, Slow-Twitch
- Muscle, Skeletal/growth & development*
- RNA, Messenger/analysis
- Receptors, Cytoplasmic and Nuclear/genetics
- Receptors, Cytoplasmic and Nuclear/physiology*
- Steroidogenic Factor 1
- Trans-Activators/physiology
- Transcription Factors/genetics
- Transcription Factors/physiology*
- Tumor Suppressor Proteins
- Zebrafish/embryology*
- Zebrafish/genetics
- PubMed
- 16162335 Full text @ Dev. Biol.
Citation
Sheela, S.G., Lee, W.C., Lin, W.W., and Chung, B.C. (2005) Zebrafish ftz-f1a (nuclear receptor 5a2) functions in skeletal muscle organization. Developmental Biology. 286(2):377-390.
Abstract
Fushi-tarazu factor 1a (Ftz-F1a, Ff1a, Nr5a2) is a nuclear receptor with diverse functions in many tissues. Here, we report the function of ff1a in zebrafish muscle differentiation. In situ hybridization revealed that ff1a mRNA was present in the adaxial and migrating slow muscle precursors and was down-regulated when slow muscle cells matured. This expression was under the control of hedgehog genes, expanded when hedgehog was increased and missing in mutants defective in genes in the Hedgehog pathway like you-too (yot), sonic you (syu), and u-boot (ubo). Blocking ff1a activity by injecting a deleted form of ff1a or an antisense ff1a morpholino oligo into fish embryos caused thinner and disorganized fibers of both slow and fast properties. Transient expression of ff1a in syu, ubo, and yot embryos led to more fibril bundles, even when slow myoblasts were transfated into fast properties. We showed that ff1a and prox1 complemented each other in slow myofibril assembly, but they did not affect the expression of each other. These results demonstrate that ff1a functions in both slow and fast muscle morphogenesis in response to Hedgehog signaling, and this function parallels the activity of another slow muscle gene, prox1.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping