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Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains

Marigo, Valeria, Nigro, Alessandra, Pecci, Alessandro, Montanaro, Donatella, Di Stazio, Mariateresa, Balduini, Carlo L., Savoia, Anna·2004·Genomics

Abstract

Nonmuscle myosin heavy chain II-A is responsible for MYH9-related disease, which is characterized by macrothrombocytopenia, granulocyte inclusions, deafness, cataracts, and renal failure. Since another two highly conserved nonmuscle myosins, II-B and II-C, are known, an analysis of their tissue distribution is fundamental for the understanding of their biological roles. In mouse, we found that all forms are ubiquitously expressed. However, megakaryocytic and granulocytic lineages express only II-A, suggesting that congenital features, macrothrombocytopenia, and leukocyte inclusions correlate with its exclusive presence. In kidney, eye, and ear, where clinical manifestations have a late onset, as well as in other tissues apparently not affected in patients, II-A and at least one of the other two isoforms are expressed, suggesting that II-B and II-C can partially compensate for each other. We hypothesize that cells expressing only II-A manifest the congenital defects, while tissues expressing additional myosin II isoforms show either late onset of abnormalities or no pathological sign.

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Research works printed but not linked: 33

  1. Berg, 2001, A millennial myosin census, Mol. Biol. Cell, 12, 780, 10.1091/mbc.12.4.780 · DOI
  2. Sellers, 2000, Myosins: a diverse superfamily, Biochim. Biophys. Acta, 1496, 3, 10.1016/S0167-4889(00)00005-7 · DOI
  3. Simons, 1991, Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes, Circ. Res, 69, 530, 10.1161/01.RES.69.2.530 · DOI
  4. Leal, 2003, A novel myosin heavy chain gene in human chromosome 19q13.3, Gene, 312, 165, 10.1016/S0378-1119(03)00613-9 · DOI
  5. Buxton, 2003, Induction of nonmuscle myosin heavy chain II-C by butyrate in RAW 264.7 mouse macrophages, J. Biol. Chem, 278, 15449, 10.1074/jbc.M210145200 · DOI
  6. Seri, 2003, MYH9-related disease: May–Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness, Medicine, 82, 203, 10.1097/01.md.0000076006.64510.5c · DOI
  7. The May–Hegglin/Fechtner Syndrome Consortium, 2000, Mutations in MYH9 result in the May–Hegglin anomaly, and Fechtner and Sebastian syndromes, Nat. Genet, 26, 103, 10.1038/79063 · DOI
  8. Kelley, 2000, Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May–Hegglin anomaly, Nat. Genet, 26, 106, 10.1038/79069 · DOI
  9. Kunishima, 2001, Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May–Hegglin anomaly/Sebastian syndrome), Blood, 97, 1147, 10.1182/blood.V97.4.1147 · DOI
  10. Kunishima, 2001, Identification of six novel MYH9 mutations and genotype–phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions, J. Hum. Genet, 46, 722, 10.1007/s100380170007 · DOI
  11. Arrondel, 2002, Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes, J. Am. Soc. Nephrol, 13, 65, 10.1681/ASN.V13165 · DOI
  12. Seri, 2002, Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene, Hum. Genet, 110, 182, 10.1007/s00439-001-0659-1 · DOI
  13. Pecci, 2002, Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders, Br. J. Haematol, 117, 164, 10.1046/j.1365-2141.2002.03385.x · DOI
  14. Kunishima, 2003, Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations, Lab. Invest, 83, 115, 10.1097/01.LAB.0000050960.48774.17 · DOI
  15. Kolega, 1998, Cytoplasmic dynamics of myosin IIA and IIB: spatial ‘sorting’ of isoforms in locomoting cells, J. Cell Sci, 111, 2085, 10.1242/jcs.111.15.2085 · DOI
  16. Kawamoto, 1991, Chicken nonmuscle myosin heavy chains: differential expression of two mRNAs and evidence for two different polypeptides, J. Cell Biol, 112, 915, 10.1083/jcb.112.5.915 · DOI
  17. Rochlin, 1995, Localization of myosin II A and B isoforms in cultured neurons, J. Cell Sci, 108, 3661, 10.1242/jcs.108.12.3661 · DOI
  18. Oostendorp, 2002, Stromal cell lines from mouse aorta–gonads–mesonephros subregions are potent supporters of hematopoietic stem cell activity, Blood, 99, 1183, 10.1182/blood.V99.4.1183 · DOI
  19. Okuda, 1996, AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis, Cell, 84, 321, 10.1016/S0092-8674(00)80986-1 · DOI · Paper page
  20. Satake, 1995, Expression of the Runt domain-encoding PEBP2 alpha genes in T cells during thymic development, Mol. Cell. Biol, 15, 1662, 10.1128/MCB.15.3.1662 · DOI
  21. Tullio, 1997, Nonmuscle myosin II-B is required for normal development of the mouse heart, Proc. Natl. Acad. Sci. USA, 94, 12407, 10.1073/pnas.94.23.12407 · DOI
  22. Murakami, 1993, Changes in expression of nonmuscle myosin heavy chain isoforms during muscle and nonmuscle tissue development, Dev. Biol, 157, 19, 10.1006/dbio.1993.1108 · DOI
  23. Uren, 2000, Gene dosage affects the cardiac and brain phenotype in nonmuscle myosin II-B-depleted mice, J. Clin. Invest, 105, 663, 10.1172/JCI8199 · DOI
  24. Golomb, 2004, Identification and characterization of nonmuscle myosin II-C, a new member of the myosin II family, J. Biol. Chem, 279, 2800, 10.1074/jbc.M309981200 · DOI
  25. Choi, 1996, Cloning of the cDNA encoding rat myosin heavy chain-A and evidence for the absence of myosin heavy chain-B in cultured rat mast (RBL-2H3) cells, J. Muscle Res. Cell Motil, 17, 69, 10.1007/BF00140325 · DOI
  26. Lalwani, 2000, Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9, Am. J. Hum. Genet, 67, 1121, 10.1086/321212 · DOI
  27. Lalwani, 1997, A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration, Audiol. Neurootol, 2, 139, 10.1159/000259237 · DOI
  28. Ghiggeri, 2003, Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome), Am. J. Kidney Dis, 41, 95, 10.1053/ajkd.2003.50028 · DOI
  29. Morsli, 1999, Otx1 and Otx2 activities are required for the normal development of the mouse inner ear, Development, 126, 2335, 10.1242/dev.126.11.2335 · DOI
  30. Surace, 2000, Expression pattern of the ocular albinism type 1 (Oa1) gene in the murine retinal pigment epithelium, Invest. Ophthalmol. Visual Sci, 41, 4333
  31. Chirivi, 1994, Inhibition of the metastatic spread and growth of B16-BL6 murine melanoma by a synthetic matrix metalloproteinase inhibitor, Int. J. Cancer, 58, 460, 10.1002/ijc.2910580326 · DOI
  32. Chiavegato, 1996, Expression of non-muscle myosin isoforms in rabbit myometrium is estrogen-dependent, Cell Tissue Res, 283, 7, 10.1007/s004410050507 · DOI
  33. Conrad, 1995, Differential localization of cytoplasmic myosin II isoforms A and B in avian interphase and dividing embryonic and immortalized cardiomyocytes and other cell types in vitro, Cell Motil. Cytoskeleton, 31, 93, 10.1002/cm.970310203 · DOI

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Metadata

Authors
Marigo, V., Nigro, A., Pecci, A., Montanaro, D., Di Stazio, M., Balduini, C. L., & Savoia, A.
Venue
Genomics
Publisher
Elsevier BV
Published
2004-06
Volume
83
Issue
6
Pages
1125-1133
ISSN
0888-7543
Cited by
64
References
0
Language
en

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Marigo, V., Nigro, A., Pecci, A., Montanaro, D., Di Stazio, M., Balduini, C. L., & Savoia, A. (2004). Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains. Genomics. https://doi.org/10.1016/j.ygeno.2003.12.012