MYL3

Myosin essential light chain (ELC), ventricular/cardiac isoform is a protein that in humans is encoded by the MYL3 gene.[5][6][7] This cardiac ventricular/slow skeletal ELC isoform is distinct from that expressed in fast skeletal muscle (MYL1) and cardiac atrial muscle (MYL4). Ventricular ELC is part of the myosin molecule and is important in modulating cardiac muscle contraction.

MYL3
Identifiers
AliasesMYL3, CMH8, MLC1SB, MLC1V, VLC1, MLC-lV/sb, VLCl, myosin light chain 3
External IDsOMIM: 160790 MGI: 97268 HomoloGene: 20099 GeneCards: MYL3
Orthologs
SpeciesHumanMouse
Entrez

4634

17897

Ensembl

ENSG00000160808

ENSMUSG00000059741

UniProt

P08590

P09542

RefSeq (mRNA)

NM_000258

NM_010859
NM_001364484

RefSeq (protein)

NP_000249
NP_000249.1

NP_034989
NP_001351413

Location (UCSC)Chr 3: 46.84 – 46.88 MbChr 9: 110.57 – 110.6 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Structure

Cardiac, ventricular ELC is 21.9 kDa and composed of 195 amino acids (See human MYL3 sequences features here). Cardiac ELC and the second light chain, regulatory light chain (RLC, MYL2), are non-covalently bound to IQXXXRGXXXR motifs in the 9 nm S1-S2 lever arm of the myosin head,[8] both alpha (MYH6) and beta (MYH7) isoforms. Both light chains are members of the EF-hand superfamily of proteins, which possess helix-loop-helix motifs in two globular domains connected by an alpha-helical linker. Though EF hand motifs are specialized to bind divalent ions such as calcium, cardiac ELC does not bind calcium at physiological levels.[9] The N-terminal region of cardiac ELC is functionally unique in that it is positively charged, being rich in Lysine residues (amino acids 4-14), with subsequent unique structure governed by proline-alanine repeats (amino acids 15-36).

Function

Studies have provided evidence for ELC as modulator of myosin crossbridge kinetics. Treating cardiac myofibrils with the lysine-rich N-terminal peptide (amino acids 5-14) evoked a supramaximal increase in cardiac myofibrillar MgATPase activity at submaximal calcium concentrations,[10] and further studies demonstrated that this region of ELC modulates the affinity of myosin for actin.[11]

Clinical significance

Mutations in MYL3 have been identified as a cause of familial hypertrophic cardiomyopathy, and associated with a mid-left ventricular chamber type hypertrophy.[12] Five mutations in MYL3 have been identified to date: M149V, R154H, E56G, A57G and E143K.[13][14][15][16] All of these cluster around two of the four EF-hand domains, suggesting that proper conformation in these regions is necessary for normal cardiac function.[12]

References
  1. GRCh38: Ensembl release 89: ENSG00000160808 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000059741 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Shi Q, Li RK, Mickle DA, Jackowski G (November 1992). "Analysis of the upstream regulatory region of human ventricular myosin light chain 1 gene". Journal of Molecular and Cellular Cardiology. 24 (11): 1221–9. doi:10.1016/0022-2828(92)93089-3. PMID 1479618.
  6. Cohen-Haguenauer O, Barton PJ, Van Cong N, Cohen A, Masset M, Buckingham M, Frézal J (February 1989). "Chromosomal assignment of two myosin alkali light-chain genes encoding the ventricular/slow skeletal muscle isoform and the atrial/fetal muscle isoform (MYL3, MYL4)". Human Genetics. 81 (3): 278–82. doi:10.1007/bf00279004. PMID 2784124. S2CID 6703175.
  7. "Entrez Gene: MYL3 myosin, light chain 3, alkali; ventricular, skeletal, slow".
  8. Rayment I, Rypniewski WR, Schmidt-Bäse K, Smith R, Tomchick DR, Benning MM, Winkelmann DA, Wesenberg G, Holden HM (July 1993). "Three-dimensional structure of myosin subfragment-1: a molecular motor". Science. 261 (5117): 50–8. Bibcode:1993Sci...261...50R. doi:10.1126/science.8316857. PMID 8316857.
  9. Collins JH (February 1991). "Myosin light chains and troponin C: structural and evolutionary relationships revealed by amino acid sequence comparisons". Journal of Muscle Research and Cell Motility. 12 (1): 3–25. doi:10.1007/bf01781170. PMID 2050809. S2CID 27878606.
  10. Rarick HM, Opgenorth TJ, von Geldern TW, Wu-Wong JR, Solaro RJ (October 1996). "An essential myosin light chain peptide induces supramaximal stimulation of cardiac myofibrillar ATPase activity". The Journal of Biological Chemistry. 271 (43): 27039–43. doi:10.1074/jbc.271.43.27039. PMID 8900193.
  11. Stepkowski D, Efimova N, Paczyņska A, Moczarska A, Nieznańska H, Kakol I (June 1997). "The possible role of myosin A1 light chain in the weakening of actin-myosin interaction". Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1340 (1): 105–14. doi:10.1016/s0167-4838(97)00031-9. PMID 9217020.
  12. Harris SP, Lyons RG, Bezold KL (March 2011). "In the thick of it: HCM-causing mutations in myosin binding proteins of the thick filament". Circulation Research. 108 (6): 751–64. doi:10.1161/CIRCRESAHA.110.231670. PMC 3076008. PMID 21415409.
  13. Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, Sellers JR, Fananapazir L, Epstein ND (May 1996). "Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle". Nature Genetics. 13 (1): 63–9. doi:10.1038/ng0596-63. PMID 8673105. S2CID 742106.
  14. Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M (May 2003). "Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy". Circulation. 107 (17): 2227–32. doi:10.1161/01.CIR.0000066323.15244.54. PMID 12707239.
  15. Lee W, Hwang TH, Kimura A, Park SW, Satoh M, Nishi H, Harada H, Toyama J, Park JE (February 2001). "Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy". American Heart Journal. 141 (2): 184–9. doi:10.1067/mhj.2001.112487. PMID 11174330. S2CID 23534623.
  16. Olson TM, Karst ML, Whitby FG, Driscoll DJ (May 2002). "Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology". Circulation. 105 (20): 2337–40. doi:10.1161/01.cir.0000018444.47798.94. PMID 12021217.

Further reading
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.