Wikipedia

Dystrophin

(Redirected from DMD (gene))

Dystrophin is a rod-shaped cytoplasmic protein, and a vital part of a protein complex that connects the cytoskeleton of a muscle fiber to the surrounding extracellular matrix through the cell membrane. This complex is variously known as the costamere or the dystrophin-associated protein complex (DAPC). Many muscle proteins, such as α-dystrobrevin, syncoilin, synemin, sarcoglycan, dystroglycan, and sarcospan, colocalize with dystrophin at the costamere. It has a molecular weight of 427 kDa [5][6]

DMD
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDMD, BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85, dystrophin
External IDsOMIM: 300377; MGI: 94909; HomoloGene: 20856; GeneCards: DMD; OMA:DMD - orthologs
Orthologs
SpeciesHumanMouse
Entrez

1756

13405

Ensembl

ENSG00000198947

ENSMUSG00000045103

UniProt

P11532

P11531

RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)Chr X: 31.1 – 33.34 MbChr X: 81.99 – 84.25 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
In humans, the DMD gene is located on the short (p) arm of the X chromosome between positions 21.2 and 21.1

Dystrophin is coded for by the DMD gene – the largest known human gene, covering 2.4 megabases (0.08% of the human genome) at locus Xp21. The primary transcript in muscle measures about 2,100 kilobases and takes 16 hours to transcribe;[7] the mature mRNA measures 14.0 kilobases.[8] The 79-exon muscle transcript[9] codes for a protein of 3685 amino acid residues.[10]

Spontaneous or inherited mutations in the dystrophin gene can cause different forms of muscular dystrophy, a disease characterized by progressive muscular wasting. The most common of these disorders caused by genetic defects in dystrophin is Duchenne muscular dystrophy.

Function

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Dystrophin is a protein located between the sarcolemma and the outermost layer of myofilaments in the muscle fiber (myofiber). It is a cohesive protein, linking actin filaments to other support proteins that reside on the inside surface of each muscle fiber's plasma membrane (sarcolemma). These support proteins on the inside surface of the sarcolemma in turn links to two other consecutive proteins for a total of three linking proteins. The final linking protein is attached to the fibrous endomysium of the entire muscle fiber. Dystrophin supports muscle fiber strength, and the absence of dystrophin reduces muscle stiffness, increases sarcolemmal deformability, and compromises the mechanical stability of costameres and their connections to nearby myofibrils. This has been shown in recent studies where biomechanical properties of the sarcolemma and its links through costameres to the contractile apparatus were measured,[11] and helps to prevent muscle fiber injury. Movement of thin filaments (actin) creates a pulling force on the extracellular connective tissue that eventually becomes the tendon of the muscle. The dystrophin associated protein complex also helps scaffold various signalling and channel proteins, implicating the DAPC in regulation of signalling processes.[12]

Pathology

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Dystrophin deficiency has been definitively established as one of the root causes of the general class of myopathies collectively referred to as muscular dystrophy. The deletions of one or several exons of the dystrophin DMD gene cause Duchenne and Becker muscular dystrophies.[13] The large cytosolic protein was first identified in 1987 by Louis M. Kunkel,[14] after concurrent works by Kunkel and Robert G. Worton to characterize the mutated gene that causes Duchenne muscular dystrophy (DMD).[15][16] At least nine disease-causing mutations in this gene have been discovered.[17]

Normal skeletal muscle tissue contains only small amounts of dystrophin (about 0.002% of total muscle protein),[14] but its absence (or abnormal expression) leads to the development of a severe and currently incurable constellation of symptoms most readily characterized by several aberrant intracellular signaling pathways that ultimately yield pronounced myofiber necrosis as well as progressive muscle weakness and fatigability. Most DMD patients become wheelchair-dependent early in life, and the gradual development of cardiac hypertrophy—a result of severe myocardial fibrosis—typically results in premature death in the first two or three decades of life. Variants (mutations) in the DMD gene that lead to the production of too little or a defective, internally shortened but partially functional dystrophin protein, result in a display of a much milder dystrophic phenotype in affected patients, resulting in the disease known as Becker's muscular dystrophy (BMD). In some cases, the patient's phenotype is such that experts may decide differently on whether a patient should be diagnosed with DMD or BMD. The theory currently most commonly used to predict whether a variant will result in a DMD or BMD phenotype, is the reading frame rule.[18]

Though its role in airway smooth muscle is not well established, recent research indicates that dystrophin along with other subunits of dystrophin glycoprotein complex is associated with phenotype maturation.[19]

Research

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A number of models are used to facilitate research on DMD gene defects. These include the mdx mouse, GRMD (golden retriever muscular dystrophy) dog, and HFMD (hypertrophic feline muscular dystrophy) cat.[20]

The mdx mouse contains a nonsense mutation in exon 23, leading to a shortened dystrophin protein.[21] Levels of dystrophin in this model is not zero: a variety of mutation alleles exist with measurable levels certain of dystrophin isoforms.[20] Muscle degeneration pathology is most easily visible in the diaphragm.[22] Generally, clinically relevant pathology is observed with older mdx mice.[22]

The GRMD dog is one of several existing dystrophin-deficient dogs identified where substantial characterization has been performed.[23] Clinically relevant pathology can be observed at 8 weeks after birth, with continued gradual deterioration of muscle function.[24] Muscle histology is most analogous to clinical presentation of DMD in humans with necrosis, fibrosis and regeneration.[25]

The HFMD cat has a deletion in the promoter region of the DMD gene.[26] Muscle histology shows necrosis but no fibrosis.[27] Extensive hypertrophy has been observed which is thought to be responsible for shorter lifespans.[28][27] Due to the hypertrophy, this model may have limited uses for DMD studies.  

Therapeutic microdystrophin

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Interactions

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Dystrophin has been shown to interact with:

Neanderthal admixture

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A variant of the DMD gene, which is on the X chromosome, named B006, appears to be an introgression from a Neanderthal-modern human mating.[37]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000198947 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000045103 – 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. ^ Lederfein D, Levy Z, Augier N, Mornet D, Morris G, Fuchs O, et al. (June 1992). "A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues". Proceedings of the National Academy of Sciences of the United States of America. 89 (12): 5346–50. Bibcode:1992PNAS...89.5346L. doi:10.1073/pnas.89.12.5346. PMC 49288. PMID 1319059.
  6. ^ "DMD - Dystrophin - Homo sapiens (Human) - DMD gene & protein". www.uniprot.org. Retrieved 1 December 2021.
  7. ^ Tennyson CN, Klamut HJ, Worton RG (February 1995). "The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced". Nature Genetics. 9 (2): 184–90. doi:10.1038/ng0295-184. PMID 7719347. S2CID 7858296.
  8. ^ NCBI Sequence Viewer v2.0
  9. ^ Strachan T and Read AP, 1999. Human molecular genetics, BIOS Scientific, New York, USA
  10. ^ "dystrophin isoform Dp427c [Homo sapiens] - Protein - NCBI". www.ncbi.nlm.nih.gov.
  11. ^ García-Pelagio KP, Bloch RJ, Ortega A, González-Serratos H (March 2011). "Biomechanics of the sarcolemma and costameres in single skeletal muscle fibers from normal and dystrophin-null mice". Journal of Muscle Research and Cell Motility. 31 (5–6): 323–36. doi:10.1007/s10974-011-9238-9. PMC 4326082. PMID 21312057.
  12. ^ Constantin B (February 2014). "Dystrophin complex functions as a scaffold for signalling proteins". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1838 (2): 635–42. doi:10.1016/j.bbamem.2013.08.023. PMID 24021238.
  13. ^ Le Rumeur E (July 2015). "Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies". Bosnian Journal of Basic Medical Sciences. 15 (3): 14–20. doi:10.17305/bjbms.2015.636. PMC 4594321. PMID 26295289.
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  19. ^ Sharma P, Tran T, Stelmack GL, McNeill K, Gosens R, Mutawe MM, Unruh H, Gerthoffer WT, Halayko AJ (January 2008). "Expression of the dystrophin-glycoprotein complex is a marker for human airway smooth muscle phenotype maturation". American Journal of Physiology. Lung Cellular and Molecular Physiology. 294 (1): L57–68. doi:10.1152/ajplung.00378.2007. PMID 17993586.
  20. ^ a b Blake DJ, Weir A, Newey SE, Davies KE (April 2002). "Function and genetics of dystrophin and dystrophin-related proteins in muscle". Physiological Reviews. 82 (2): 291–329. doi:10.1152/physrev.00028.2001. PMID 11917091.
  21. ^ Sicinski P, Geng Y, Ryder-Cook AS, Barnard EA, Darlison MG, Barnard PJ (June 1989). "The molecular basis of muscular dystrophy in the mdx mouse: a point mutation". Science. 244 (4912): 1578–80. Bibcode:1989Sci...244.1578S. doi:10.1126/science.2662404. PMID 2662404.
  22. ^ a b Stedman HH, Sweeney HL, Shrager JB, Maguire HC, Panettieri RA, Petrof B, et al. (August 1991). "The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy". Nature. 352 (6335): 536–9. Bibcode:1991Natur.352..536S. doi:10.1038/352536a0. PMID 1865908. S2CID 4302451.
  23. ^ "Duchenne Muscular Dystrophy and Becker Muscular Dystrophy: Diagnostic Principles". Duchenne Muscular Dystrophy. CRC Press. 2006-02-27. pp. 105–118. doi:10.3109/9780849374456-7. ISBN 978-0-429-16351-7.
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  26. ^ Winand NJ, Edwards M, Pradhan D, Berian CA, Cooper BJ (September 1994). "Deletion of the dystrophin muscle promoter in feline muscular dystrophy". Neuromuscular Disorders. 4 (5–6): 433–45. doi:10.1016/0960-8966(94)90082-5. PMID 7881288. S2CID 38556669.
  27. ^ a b Carpenter JL, Hoffman EP, Romanul FC, Kunkel LM, Rosales RK, Ma NS, et al. (November 1989). "Feline muscular dystrophy with dystrophin deficiency". The American Journal of Pathology. 135 (5): 909–19. PMC 1880103. PMID 2683799.
  28. ^ Gaschen FP, Hoffman EP, Gorospe JR, Uhl EW, Senior DF, Cardinet GH, Pearce LK (July 1992). "Dystrophin deficiency causes lethal muscle hypertrophy in cats". Journal of the Neurological Sciences. 110 (1–2): 149–59. doi:10.1016/0022-510x(92)90022-d. PMID 1506854. S2CID 21156994.
  29. ^ "Chugai In-Licenses Gene Therapy Delandistrogene Moxeparvovec (SRP-9001) for Duchenne Muscular Dystrophy | News". 16 December 2021.
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  37. ^ Khan R (January 25, 2011). "Neandertal admixture, revisiting results after shaken priors". Discover Magazine. Archived from the original on January 27, 2013. Retrieved March 27, 2013.

Further reading

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