ArticleBMC developmental biology2007
Multiple upstream modules regulate zebrafish myf5 expression.
Article in BMC developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed, 166 citations in OpenAlex.
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- Using Transgenic Zebrafish to Study Muscle Stem/Progenitor Cells.Methods in molecular biology (Clifton, N.J.) · 2017Article
- Wnt9a Is Required for the Aortic Amplification of Nascent Hematopoietic Stem Cells.Cell reports · 2016Article
- Zebrafish and Medaka: new model organisms for modern biomedical research.Journal of biomedical science · 2016Review
- Discrete Notch signaling requirements in the specification of hematopoietic stem cells.The EMBO journal · 2014Article
- Protective Role of Comfrey Leave Extracts on UV-induced Zebrafish Fin Damage.Journal of toxicologic pathology · 2014Article
- Normal function of Myf5 during gastrulation is required for pharyngeal arch cartilage development in zebrafish embryos.Zebrafish · 2013Article
- Zebrafish rhabdomyosarcoma reflects the developmental stage of oncogene expression during myogenesis.Development (Cambridge, England) · 2013Article
- In vivo imaging of tumor-propagating cells, regional tumor heterogeneity, and dynamic cell movements in embryonal rhabdomyosarcoma.Cancer cell · 2012Article
- Essential roles of basic helix-loop-helix transcription factors, Capsulin and Musculin, during craniofacial myogenesis of zebrafish.Cellular and molecular life sciences : CMLS · 2011Article
- dickkopf-3-related gene regulates the expression of zebrafish myf5 gene through phosphorylated p38a-dependent Smad4 activity.The Journal of biological chemistry · 2011Article
- Transgenic expression of prothymosin alpha on zebrafish epidermal cells promotes proliferation and attenuates UVB-induced apoptosis.Transgenic research · 2010Article
- Novel intronic microRNA represses zebrafish myf5 promoter activity through silencing dickkopf-3 gene.Nucleic acids research · 2010Article
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Authors and funding
7 authors at 3 institutions in 2 countries.
Funding
Abstract
backgroundMyf5 is one member of the basic helix-loop-helix family of transcription factors, and it functions as a myogenic factor that is important for the specification and differentiation of muscle cells. The expression of myf5 is somite- and stage-dependent during embryogenesis through a delicate regulation. However, this complex regulatory mechanism of myf5 is not clearly understood.
resultsWe isolated a 156-kb bacterial artificial chromosome clone that includes an upstream 80-kb region and a downstream 70-kb region of zebrafish myf5 and generated a transgenic line carrying this 156-kb segment fused to a green fluorescent protein (GFP) reporter gene. We find strong GFP expression in the most rostral somite and in the presomitic mesoderm during segmentation stages, similar to endogenous myf5 expression. Later, the GFP signals persist in caudal somites near the tail bud but are down-regulated in the older, rostral somites. During the pharyngula period, we detect GFP signals in pectoral fin buds, dorsal rostral myotomes, hypaxial myotomes, and inferior oblique and superior oblique muscles, a pattern that also corresponds well with endogenous myf5 transcripts. To characterize the specific upstream cis-elements that regulate this complex and dynamic expression pattern, we also generated several transgenic lines that harbor various lengths within the upstream 80-kb segment. We find that (1) the -80 kb/-9977 segment contains a fin and cranial muscle element and a notochord repressor; (2) the -9977/-6213 segment contains a strong repressive element that does not include the notochord-specific repressor; (3) the -6212/-2938 segment contains tissue-specific elements for bone and spinal cord; (4) the -2937/-291 segment contains an eye enhancer, and the -2937/-2457 segment is required for notochord and myocyte expression; and (5) the -290/-1 segment is responsible for basal transcription in somites and the presomitic mesoderm.
conclusionWe suggest that the cell lineage-specific expression of myf5 is delicately orchestrated by multiple modules within the distal upstream region. This study provides an insight to understand the molecular control of myf5 and myogenesis in the zebrafish.
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