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A novel human muscle factor related to but distinct from MyoD1 induces myogenic conversion in 1OT1/2 fibroblasts

: Braun, T.; Bober, E.; Tannich, E.; Arnold, H.-H.; Buschhausen-Denker, G.

EMBO Journal 8 (1989), No.3, pp.701-709
ISSN: 0261-4189
Journal Article
Fraunhofer ITA ( ITEM) ()
amino acid sequence; base sequence; cDNA; cell line; DNA; genetic; human Myf-5; molecular cloning; muscle determination; muscle protein; myc-homology; transactivation

We have isolated the cDNA encoding a novel human myogenic factor, Myf-5, by weak cross-hydrization to the mouse MyoD1 probe. Nucleotide sequence analysis and the identification of corresponding gene indicate that human Myf-5 is a member of a small gene family which also contains the human homologue to MyoD1. Although structurally related to the mouse factor, the human Myf-5 constitutes a different protein which nevertheless is capable of inducing the myogenic phenotype in embryonic C3H mouse 10T1/2 fibroblasts. The existence of more than one MyoD1-like protein in human skeletal muscle is further suggested by the detection of several similar but distinct cDNA clones. The phenotypic conversion of 10T1/2 cells by the human factor is recognized by the capacity of the cells to form multinucleated synctia and synthesize sarcomeric myosin heavy chains. Moreover, transient expression of Myf-5 in 10T1/2 cells leads to the activation of a co-transfected muscle specific CAT reporter gene which by itself is transcriptionally silent in the nonmuscle cell background. The deduced amino acid sequence of clone Myf-5 reveals a region which is highly similar to myc proteins and the developmental factors from Drosophila encoded by the achaete scute locus and the twist gene. The myc homology region and a preceding cluster of basic amino acids are located in a larger sequence domain with strong similarity to the mouse myogenic factor MyoD1.