MYL1
Myosin light chain 3, skeletal muscle isoform is a protein that in humans is encoded by the MYL1 gene.[1][2][3]
Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in fast skeletal muscle. Two transcript variants have been identified for this gene.[3]
References
- ↑ Hailstones DL, Gunning PW (Mar 1990). “Characterization of human myosin light chains 1sa and 3nm: implications for isoform evolution and function”. Mol Cell Biol. 10 (3): 1095–104. PMC 360973. PMID 2304459.
- ↑ Cohen-Haguenauer O, Barton PJ, Nguyen VC, Serero S, Gross MS, Jegou-Foubert C, de Tand MF, Robert B, Buckingham M, Frezal J (Mar 1988). “Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qter”. Hum Genet. 78 (1): 65–70. doi:10.1007/BF00291237. PMID 3422212.
- ↑ 3.0 3.1 “Entrez Gene: MYL1 myosin, light chain 1, alkali; skeletal, fast”.
Further reading
- Kelly RG, Buckingham ME (2000). “Modular regulation of the MLC1F/3F gene and striated muscle diversity”. Microsc. Res. Tech. 50 (6): 510–21. doi:10.1002/1097-0029(20000915)50:6<510::AID-JEMT8>3.0.CO;2-1. PMID 10998640.
- Seidel U, Bober E, Winter B, et al. (1988). “Alkali myosin light chains in man are encoded by a multigene family that includes the adult skeletal muscle, the embryonic or atrial, and nonsarcomeric isoforms”. Gene. 66 (1): 135–46. doi:10.1016/0378-1119(88)90231-4. PMID 2458299.
- Seidel U, Arnold HH (1989). “Identification of the functional promoter regions in the human gene encoding the myosin alkali light chains MLC1 and MLC3 of fast skeletal muscle”. J. Biol. Chem. 264 (27): 16109–17. PMID 2777779.
- Seidel U, Bober E, Winter B, et al. (1987). “The complete nucleotide sequences of cDNA clones coding for human myosin light chains 1 and 3”. Nucleic Acids Res. 15 (12): 4989. doi:10.1093/nar/15.12.4989. PMC 305934. PMID 3601661.
- Kontrogianni-Konstantopoulos A, Huang SC, Benz EJ (2001). “A Nonerythroid Isoform of Protein 4.1R Interacts with Components of the Contractile Apparatus in Skeletal Myofibers”. Mol. Biol. Cell. 11 (11): 3805–17. doi:10.1091/mbc.11.11.3805. PMC 15038. PMID 11071908.
- Ballweber E, Galla M, Aktories K, et al. (2001). “Interaction of ADP-ribosylated actin with actin binding proteins”. FEBS Lett. 508 (1): 131–5. doi:10.1016/S0014-5793(01)03040-X. PMID 11707283.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Rual JF, Venkatesan K, Hao T, et al. (2005). “Towards a proteome-scale map of the human protein-protein interaction network”. Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
- Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). “Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes”. Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
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