Skip to main content

Serca pumps and human diseases

  • Chapter
Calcium Signalling and Disease

Part of the book series: Subcellular Biochemistry ((SCBI,volume 45))

Abstract

Sarco(endo)plasmic reticulum (SER) Ca2+ ATPases represent a highly conserved family of Ca2+ pumps which actively transport Ca2+ from the cytosol to the SER against a large concentration gradient. In humans, 3 genes (ATP2A1-3) generate multiple isoforms (SERCA1a,b, SERCA2a–c, SECA3a–f) by developmental or tissue-specific alternative splicing. These pumps differ by their regulatory and kinetic properties, allowing for optimized function in the tissue where they are expressed. They play a central role in calcium signalling through regenerating SER Ca2+ stores, maintaining appropriate Ca2+ levels in this organelle and shaping cytosolic and nuclear Ca2+ variations which govern cell response. Defects in ATP2A1 encoding SERCA1 cause recessive Brody myopathy, mutations in ATP2A2 coding for SERCA2 underlie a dominant skin disease, Darier diseaseand its clinical variants. SERCA2a expression is reduced in heart failure in human and in mice models. Gene-targeting studies in mouse confirmed the expected function of these isoforms in some cases, but also resulted in unexpected phenotypes: SERCA1 null mutants die from respiratory failure, SERCA2 heterozygous mutant mice develop skin cancer with age and SERCA3 null mice display no diabetes. These nique phenotypes have provided invaluable information on the role of these pumps in specific tissues and species, and have improved our understanding of Ca2+ regulated processes in muscles, the heart and the skin in human and in mice. Although the understanding of the pathogenesis of these diseases is still incomplete, these recent advances hold the promise of improved knowledge on the disease processes and the identification of new targets for therapeutic interventions

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Ahn, W., Lee, M. G., Kim, K. H., and Muallem, S., 2003, Multiple effects of SERCA2b mutations associated with Darier’s disease. J Biol Chem, 278: 20795–801.

    PubMed  CAS  Google Scholar 

  • Arredouani, A., Guiot, Y., Jonas, J. C., Liu, L. H., Nenquin, M., Pertusa, J. A., Rahier, J.,Rolland, J.F., Shull, G. E., Stevens, M., Wuytack, F., Henquin, J. C., and Gilon, P., 2002, SERCA3 ablation does not impair insulin secretion but suggests distinct roles of different sarcoendoplasmic reticulum Ca(2+) pumps for Ca(2+) homeostasis in pancreatic beta-cells. Diabetes, 51: 3245–53.

    PubMed  CAS  Google Scholar 

  • Asahi, M., Sugita, Y., Kurzydlowski, K., De Leon, S., Tada, M., Toyoshima, C., and MacLennan, D. H., 2003, Sarcolipin regulates sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) by binding to transmembrane helices alone or in association with phospholamban. Proc Natl Acad Sci U S A, 100: 5040–5.

    PubMed  CAS  Google Scholar 

  • Baba-Aissa, F., Raeymaekers, L., Wuytack, F., Dode, L., and Casteels, R., 1998, Distribution and isoform diversity of the organellar Ca2+ pumps in the brain. Mol Chem Neuropathol, 33: 199–208.

    PubMed  CAS  Google Scholar 

  • Benders, A. A., Veerkamp, J. H., Oosterhof, A., Jongen, P. J., Bindels, R. J., Smit, L. M., Busch, H. F., and Wevers, R. A., 1994, Ca2+ homeostasis in Brody’s disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil. J Clin Invest, 94: 741–8.

    PubMed  CAS  Google Scholar 

  • Berridge, M. J., 2002, The endoplasmic reticulum: a multifunctional signaling organelle. Cell Calcium, 32: 235–49.

    PubMed  CAS  Google Scholar 

  • Bobe, R., Bredoux, R., Corvazier, E., Andersen, J. P., Clausen, J. D., Dode, L., Kovacs, T., and Enouf, J., 2004, Identification, expression, function, and localization of a novel (sixth) isoform of the human sarco/endoplasmic reticulum Ca2+ ATPase 3 gene. J Biol Chem, 279: 24297–306.

    PubMed  CAS  Google Scholar 

  • Brandl, C. J., Green, N. M., Korczak, B., and MacLennan, D. H., 1986, Two Ca2+ ATPase genes: homologies and mechanistic implications of deduced amino acid sequences. Cell, 44: 597–607.

    PubMed  CAS  Google Scholar 

  • Brini, M., and Carafoli, E., 2000, Calcium signalling: a historical account, recent developments and future perspectives. Cell Mol Life Sci, 57: 354–70.

    PubMed  CAS  Google Scholar 

  • Brody, I. A., 1969, Muscle contracture induced by exercise. A syndrome attributable to decreased relaxing factor. N Engl J Med, 281: 187–92.

    PubMed  CAS  Google Scholar 

  • Callen, D. F., Baker, E., Lane, S., Nancarrow, J., Thompson, A., Whitmore, S. A., MacLennan, D. H., Berger, R., Cherif, D., Jarvela, I., and et al., 1991, Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12. Am J Hum Genet, 49: 1372–7.

    PubMed  CAS  Google Scholar 

  • Carafoli, E., and Brini, M., 2000, Calcium pumps: structural basis for and mechanism of calcium transmembrane transport. Curr Opin Chem Biol, 4: 152–61.

    PubMed  CAS  Google Scholar 

  • Carafoli, E., Santella, L., Branca, D., and Brini, M., 2001, Generation, control, and processing of cellular calcium signals. Crit Rev Biochem Mol Biol, 36: 107–260.

    PubMed  CAS  Google Scholar 

  • Cooper, S. M., and Burge, S. M., 2003, Darier’s disease: epidemiology, pathophysiology, and management. Am J Clin Dermatol, 4: 97–105.

    PubMed  Google Scholar 

  • Craddock, N., Burge, S., Parfitt, L., and Owen, M., 1993, Linkage is excluded between Darier’s disease and the Duffy blood group locus in five British families. Ann Genet, 36: 211–3.

    PubMed  CAS  Google Scholar 

  • Craddock, N., Owen, M., Burge, S., Kurian, B., Thomas, P., and McGuffin, P., 1994, Familial cosegregation of major affective disorder and Darier’s disease (keratosis follicularis). Br J Psychiatry, 164: 355–8.

    PubMed  CAS  Google Scholar 

  • Dally, S., Bredoux, R., Corvazier, E., Andersen, J. P., Clausen, J. D., Dode, L., Fanchaouy, M., Gelebart, P., Monceau, V., Del Monte, F., Gwathmey, J. K., Hajjar, R., Chaabane, C., Bobe, R., Raies, A., and Enouf, J., 2006, Ca2+-ATPases in non-failing and failing heart: evidence for a novel cardiac sarco/endoplasmic reticulum Ca2+-ATPase 2 isoform (SERCA2c). Biochem J, 395: 249–58.

    PubMed  CAS  Google Scholar 

  • Dhitavat, J., Cobbold, C., Leslie, N., Burge, S., and Hovnanian, 2003a, A. Impaired trafficking of the desmoplakins in cultured Darier’s disease keratinocytes. J Invest Dermatol, 121: 1349–55.

    Google Scholar 

  • Dhitavat, J., Dode, L., Leslie, N., Sakuntabhai, A., Lorette, G., and Hovnanian, A., 2003b, Mutations in the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase isoform cause Darier’s disease. J Invest Dermatol, 121: 486–9.

    CAS  Google Scholar 

  • Dhitavat, J., Macfarlane, S., Dode, L., Leslie, N., Sakuntabhai, A., MacSween, R., Saihan, E., and Hovnanian, A., 2003c, Acrokeratosis verruciformis of Hopf is caused by mutation in ATP2A2: evidence that it is allelic to Darier’s disease. J Invest Dermatol, 120: 229–32.

    CAS  Google Scholar 

  • Dode, L., Andersen, J. P., Leslie, N., Dhitavat, J., Vilsen, B., and Hovnanian, A., 2003, Dissection of the functional differences between sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) 1 and 2 isoforms and characterization of Darier disease (SERCA2) mutants by steady-state and transient kinetic analyses. J Biol Chem, 278: 47877–89.

    Google Scholar 

  • Dode, L., De Greef, C., Mountian, I., Attard, M., Town, M. M., Casteels, R., and Wuytack, F., 1998, Structure of the human sarco/endoplasmic reticulum Ca2+-ATPase 3 gene. Promoter analysis and alternative splicing of the SERCA3 pre-mRNA. J Biol Chem, 273: 13982–94.

    PubMed  CAS  Google Scholar 

  • Dode, L., Vilsen, B., Van Baelen, K., Wuytack, F., Clausen, J. D., and Andersen, J. P., 2002, Dissection of the functional differences between sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) 1 and 3 isoforms by steady-state and transient kinetic analyses. J Biol Chem, 277: 45579–91.

    PubMed  CAS  Google Scholar 

  • Dogliotti, M., and Schmaman, A., 1971, Acrokeratosis verruciformis: malignant transformation. Dermatologica, 143: 95–9.

    PubMed  CAS  Google Scholar 

  • Ellgaard, L., and Helenius, A., 2003, Quality control in the endoplasmic reticulum. Nat Rev Mol Cell Biol, 4: 181–91.

    PubMed  CAS  Google Scholar 

  • Foggia, L., Aronchik, I., Aberg, K., Brown, B., Hovnanian, A., and Mauro, T. M., 2006, Activity of the hSPCA1 Golgi Ca2+ pump is essential for Ca2+-mediated Ca2+ response and cell viability in Darier disease. J Cell Sci, 119: 671–9.

    PubMed  CAS  Google Scholar 

  • Foggia, L., and Hovnanian, A., 2004, Calcium pump disorders of the skin. Am J Med Genet C Semin Med Genet, 131C: 20–31.

    PubMed  Google Scholar 

  • Foresman, P. L., Goldsmith, L. A., Ginn, L., and Beck, A. L., 1993, Hemorrhagic Darier’s disease. Arch Dermatol, 129: 511–2.

    PubMed  CAS  Google Scholar 

  • Frezzini, C., Cedro, M., Leao, J. C., and Porter, S., 2006, Darier disease affecting the gingival and oral mucosal surfaces. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 102: e29–33.

    PubMed  Google Scholar 

  • Gelebart, P., Martin, V., Enouf, J., and Papp, B., 2003, Identification of a new SERCA2 splice variant regulated during monocytic differentiation. Biochem Biophys Res Commun, 303: 676–84.

    PubMed  CAS  Google Scholar 

  • Godic, A., Glavac, D., Korosec, B., Miljkovic, J., Potocnik, M., and Kansky, A., 2004, P160L mutation in the Ca(2+) ATPase 2A domain in a patient with severe Darier disease. Dermatology, 209: 142–4.

    PubMed  Google Scholar 

  • Godic, A., Miljkovic, J., Kansky, A., and Vidmar, G., 2005, Epidemiology of Darier’s Disease in Slovenia. Acta Dermatovenerol Alp Panonica Adriat, 14: 43–8.

    PubMed  Google Scholar 

  • Gommans, I. M., Vlak, M. H., de Haan, A., and van Engelen, B. G., 2002, Calcium regulation and muscle disease. J Muscle Res Cell Motil, 23: 59–63.

    PubMed  CAS  Google Scholar 

  • Green, K. J., and Gaudry, C. A., 2000, Are desmosomes more than tethers for intermediate filaments? Nat Rev Mol Cell Biol, 1: 208–16.

    PubMed  CAS  Google Scholar 

  • Hafner, O., and Vakilzadeh, F., 1997, [Acrokeratosis verruciformis-like changes in Darier disease]. Hautarzt, 48: 572–6.

    PubMed  CAS  Google Scholar 

  • Hakuno, M., Shimizu, H., Akiyama, M., Amagai, M., Wahl, J. K., Wheelock, M. J., and Nishikawa, T., 2000, Dissociation of intra- and extracellular domains of desmosomal cadherins and E-cadherin in Hailey-Hailey disease and Darier’s disease. Br J Dermatol, 142: 702–11.

    PubMed  CAS  Google Scholar 

  • Hallermann, C., and Bertsch, H. P., 2004, Two sisters with familial dyskeratotic comedones. Eur J Dermatol, 14: 214–5.

    PubMed  Google Scholar 

  • Hellstern, S., Pegoraro, S., Karim, C. B., Lustig, A., Thomas, D. D., Moroder, L., and Engel, J., 2001, Sarcolipin, the shorter homologue of phospholamban, forms oligomeric structures in detergent micelles and in liposomes. J Biol Chem, 276: 30845–52.

    PubMed  CAS  Google Scholar 

  • Herndon, J., and Wilson, J., 1966, Acrokeratosis verruciformis (Hopf) and Darier’s disease , genetic evidence for a unitary origin. Arch Derm, 93: 305–310.

    Google Scholar 

  • Hopf, G., 1931, Uber eine bisher nicht beschriebene disseminierte Keratose (Acreokeratosis verruciformis). Dermatol Z, 60: 227–250.

    Google Scholar 

  • Hovnanian, A., 2004, Darier’s disease: from dyskeratosis to endoplasmic reticulum calcium ATPase deficiency. Biochem Biophys Res Commun, 322: 1237–44.

    PubMed  CAS  Google Scholar 

  • Hu, Z., Bonifas, J. M., Beech, J., Bench, G., Shigihara, T., Ogawa, H., Ikeda, S., Mauro, T., and Epstein, E. H., Jr., 2000, Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease. Nat Genet, 24: 61–5.

    PubMed  CAS  Google Scholar 

  • Ikeda, S., Mayuzumi, N., Shigihara, T., Epstein, E. H., Jr., Goldsmith, L. A., and Ogawa, H., 2003, Mutations in ATP2A2 in patients with Darier’s disease. J Invest Dermatol, 121: 475–7.

    PubMed  CAS  Google Scholar 

  • Ikeda, S., Shigihara, T., Mayuzumi, N., Yu, X., and Ogawa, H., 2001, Mutations of ATP2C1 in Japanese patients with Hailey-Hailey disease: intrafamilial and interfamilial phenotype variations and lack of correlation with mutation patterns. J Invest Dermatol, 117: 1654–6.

    PubMed  CAS  Google Scholar 

  • Jacobsen, N. J., Franks, E. K., Elvidge, G., Jones, I., McCandless, F., O’Donovan, M. C., Owen, M. J., and Craddock, N., 2001, Exclusion of the Darier’s disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Mol Psychiatry, 6: 92–7.

    PubMed  CAS  Google Scholar 

  • Jacobsen, N. J., Lyons, I., Hoogendoorn, B., Burge, S., Kwok, P. Y., O’Donovan, M. C., Craddock, N., and Owen, M. J., 1999, ATP2A2 mutations in Darier’s disease and their relationship to neuropsychiatric phenotypes. Hum Mol Genet, 8: 1631–6.

    PubMed  CAS  Google Scholar 

  • John, L. M., Lechleiter, J. D., and Camacho, P., 1998, Differential modulation of SERCA2 isoforms by calreticulin. J Cell Biol, 142: 963–73.

    PubMed  CAS  Google Scholar 

  • Jones, I., Jacobsen, N., Green, E. K., Elvidge, G. P., Owen, M. J., and Craddock, N., 2002, Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier’s disease. Mol Psychiatry, 7: 424–7.

    PubMed  CAS  Google Scholar 

  • Karpati, G., Charuk, J., Carpenter, S., Jablecki, C., and Holland, P., 1986, Myopathy caused by a deficiency of Ca2+-adenosine triphosphatase in sarcoplasmic reticulum (Brody’s disease). Ann Neurol, 20: 38–49.

    PubMed  CAS  Google Scholar 

  • Katta, R., Reed, J., and Wolf, J. E., 2000, Cornifying Darier’s disease. Int J Dermatol, 39: 844–5.

    PubMed  CAS  Google Scholar 

  • Kiewitz, R., Acklin, C., Schafer, B. W., Maco, B., Uhrik, B., Wuytack, F., Erne, P., and Heizmann, C. W., 2003, Ca2+-dependent interaction of S100A1 with the sarcoplasmic reticulum Ca2+-ATPase2a and phospholamban in the human heart. Biochem Biophys Res Commun, 306: 550–7.

    PubMed  CAS  Google Scholar 

  • Kitajima, Y., 2002, Mechanisms of desmosome assembly and disassembly. Clin Exp Dermatol, 27: 684–90.

    PubMed  CAS  Google Scholar 

  • Kuhlbrandt, W., 2004, Biology, structure and mechanism of P-type ATPases. Nat Rev Mol Cell Biol, 5: 282–95.

    PubMed  Google Scholar 

  • Leinonen, P. T., Myllyla, R. M., Hagg, P. M., Tuukkanen, J., Koivunen, J., Peltonen, S., Oikarinen, A., Korkiamaki, T., and Peltonen, J., 2005, Keratinocytes cultured from patients with Hailey-Hailey disease and Darier disease display distinct patterns of calcium regulation. Br J Dermatol, 153: 113–7.

    PubMed  CAS  Google Scholar 

  • Levy, J., Zhu, Z., and Dunbar, J. C., 1998, The effect of glucose and calcium on Ca2+-adenosine triphosphatase in pancreatic islets isolated from a normal and a non-insulin-dependent diabetes mellitus rat model. Metabolism, 47: 185–9.

    PubMed  CAS  Google Scholar 

  • Li, Y., and Camacho, P., 2004, Ca2+-dependent redox modulation of SERCA 2b by ERp57. J Cell Biol, 164: 35–46.

    PubMed  CAS  Google Scholar 

  • Liu, L. H., Boivin, G. P., Prasad, V., Periasamy, M., and Shull, G. E., 2001, Squamous cell tumors in mice heterozygous for a null allele of Atp2a2, encoding the arco(endo)plasmic reticulum Ca2+-ATPase isoform 2 Ca2+ pump. J Biol Chem, 276: 26737–40.

    PubMed  CAS  Google Scholar 

  • Liu, L. H., Paul, R. J., Sutliff, R. L., Miller, M. L., Lorenz, J. N., Pun, R. Y., Duffy, J. J., Doetschman, T., Kimura, Y., MacLennan, D. H., Hoying, J. B., and Shull, G. E., 1997, Defective endothelium-dependent relaxation of vascular smooth muscle and endothelial cell Ca2+ signaling in mice lacking sarco(endo)plasmic reticulum Ca2+-ATPase isoform 3. J Biol Chem, 272: 30538–45.

    PubMed  CAS  Google Scholar 

  • Lytton, J., Westlin, M., and Hanley, M. R., 1991, Thapsigargin inhibits the sarcoplasmic or endoplasmic reticulum Ca-ATPase family of calcium pumps. J Biol Chem, 266: 17067–71.

    PubMed  CAS  Google Scholar 

  • Mackenzie, L., Roderick, H. L., Berridge, M. J., Conway, S. J., and Bootman, M. D., 2004, The spatial pattern of atrial cardiomyocyte calcium signalling modulates contraction. J Cell Sci, 117: 6327–37.

    PubMed  CAS  Google Scholar 

  • MacLennan, D. H., 2000, Ca2+ signalling and muscle disease. Eur J Biochem, 267: 5291–7.

    PubMed  CAS  Google Scholar 

  • MacLennan, D. H., Abu-Abed, M., and Kang, C., 2002, Structure-function relationships in Ca(2+) cycling proteins. J Mol Cell Cardiol, 34: 897–918.

    PubMed  CAS  Google Scholar 

  • MacLennan, D. H., Asahi, M., and Tupling, A. R., 2003, The regulation of SERCA-type pumps by phospholamban and sarcolipin. Ann N Y Acad Sci, 986: 472–80.

    PubMed  CAS  Google Scholar 

  • MacLennan, D. H., and Kranias, E. G., 2003, Phospholamban: a crucial regulator of cardiac contractility. Nat Rev Mol Cell Biol, 4: 566–77.

    PubMed  CAS  Google Scholar 

  • MacLennan, D. H., Toyofuku, T., and Kimura, Y., 1997, Sites of regulatory interaction between calcium ATPases and phospholamban. Basic Res Cardiol, 92 Suppl 1: 11–5.

    PubMed  CAS  Google Scholar 

  • Martin, V., Bredoux, R., Corvazier, E., Van Gorp, R., Kovacs, T., Gelebart, P., and Enouf, J., 2002, Three novel sarco/endoplasmic reticulum Ca2+-ATPase (SERCA) 3 isoforms. Expression, regulation, and function of the membranes of the SERCA3 family. J Biol Chem, 277: 24442–52.

    PubMed  CAS  Google Scholar 

  • Mayosi, B. M., Kardos, A., Davies, C. H., Gumedze, F., Hovnanian, A., Burge, S., and Watkins, H., 2006, Heterozygous disruption of SERCA2a is not associated with impairment of cardiac performance in humans: implications for SERCA2a as a therapeutic target in heart failure. Heart, 92: 105–9.

    PubMed  CAS  Google Scholar 

  • Mayuzumi, N., Ikeda, S., Kawada, H., and Ogawa, H., 2005, Effects of drugs and anticytokine antibodies on expression of ATP2A2 and ATP2C1 in cultured normal human keratinocytes. Br J Dermatol, 152: 920–4.

    PubMed  CAS  Google Scholar 

  • Michalak, M., Robert Parker, J. M., and Opas, M., 2002, Ca2+ signaling and calcium binding chaperones of the endoplasmic reticulum. Cell Calcium, 32: 269–78.

    PubMed  CAS  Google Scholar 

  • Missiaen, L., Robberecht, W., van den Bosch, L., Callewaert, G., Parys, J. B., Wuytack, F., Raeymaekers, L., Nilius, B., Eggermont, J., and De Smedt, H., 2000, Abnormal intracellular Ca(2+)homeostasis and disease. Cell Calcium, 28: 1–21.

    PubMed  CAS  Google Scholar 

  • Miyauchi, Y., Daiho, T., Yamasaki, K., Takahashi, H., Ishida-Yamamoto, A., Danko, S., Suzuki, H., and Iizuka, H., 2006, Comprehensive analysis of expression and function of 51 sarco(endo)plasmic reticulum Ca2+-ATPase mutants associated with Darier disease. J Biol Chem, 281: 22882–95.

    PubMed  CAS  Google Scholar 

  • Munro, C. S., and Cox, N. H., 1992, An acantholytic dyskeratotic epidermal naevus with other features of Darier’s disease on the same side of the body. Br J Dermatol, 127: 168–71.

    PubMed  CAS  Google Scholar 

  • Niedleman, M. L., and Mc, K. V., 1962, Acrokeratosis verruciformis (Hopf). A follow-up study. Arch Dermatol, 86: 779–82.

    PubMed  CAS  Google Scholar 

  • Odermatt, A., Barton, K., Khanna, V. K., Mathieu, J., Escolar, D., Kuntzer, T., Karpati, G., and MacLennan, D. H., 2000, The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease. Hum Genet, 106: 482–91.

    PubMed  CAS  Google Scholar 

  • Odermatt, A., Taschner, P. E., Khanna, V. K., Busch, H. F., Karpati, G., Jablecki, C. K., Breuning, M. H., and MacLennan, D. H., 1996, Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease. Nat Genet, 14: 191–4.

    PubMed  CAS  Google Scholar 

  • Odermatt, A., Taschner, P. E., Scherer, S. W., Beatty, B., Khanna, V. K., Cornblath, D. R., Chaudhry, V., Yee, W. C., Schrank, B., Karpati, G., Breuning, M. H., Knoers, N., and MacLennan, D. H., 1997, Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease. Genomics, 45: 541–53.

    PubMed  CAS  Google Scholar 

  • Onozuka, T., Sawamura, D., Yokota, K., and Shimizu, H., 2004, Mutational analysis of the ATP2A2 gene in two Darier disease families with intrafamilial variability. Br J Dermatol, 150: 652–7.

    PubMed  CAS  Google Scholar 

  • Pan, Y., Zvaritch, E., Tupling, A. R., Rice, W. J., de Leon, S., Rudnicki, M., McKerlie, C., Banwell, B. L., and MacLennan, D. H., 2003, Targeted disruption of the ATP2A1 gene encoding the sarco(endo)plasmic reticulum Ca2+ ATPase isoform 1 (SERCA1) impairs diaphragm function and is lethal in neonatal mice. J Biol Chem, 278: 13367–75.

    PubMed  CAS  Google Scholar 

  • Pani, B., Cornatzer, E., Cornatzer, W., Shin, D. M., Pittelkow, M. R., Hovnanian, A., Ambudkar, I. S., and Singh, B. B., 2006, Up-regulation of transient receptor potential canonical 1 (TRPC1) following sarco(endo)plasmic reticulum Ca2+ ATPase 2 gene silencing promotes cell survival: a potential role for TRPC1 in Darier’s disease. Mol Biol Cell, 17: 4446–58.

    PubMed  CAS  Google Scholar 

  • Panja, R. K., 1977, Acrokeratosis verruciformis: (Hopf)–A clinical entity? Br J Dermatol, 96: 643–52.

    PubMed  CAS  Google Scholar 

  • Parekh, A. B., and Putney, J. W., Jr., 2005, Store-operated calcium channels. Physiol Rev, 85: 757–810.

    PubMed  CAS  Google Scholar 

  • Penrod, J. N., Everett, M. A., and Mc, C. W., 1960, Observations on keratosis follicularis. Arch Dermatol, 82: 367–70.

    PubMed  CAS  Google Scholar 

  • Periasamy, M., and Kalyanasundaram, A., 2007, SERCA pump isoforms: Their role in calcium transport and disease. Muscle Nerve.

    Google Scholar 

  • Periasamy, M., Reed, T. D., Liu, L. H., Ji, Y., Loukianov, E., Paul, R. J., Nieman, M. L., Riddle, T., Duffy, J. J., Doetschman, T., Lorenz, J. N., and Shull, G. E., 1999, Impaired cardiac performance in heterozygous mice with a null mutation in the sarco(endo)plasmic reticulum Ca2+-ATPase isoform 2 (SERCA2) gene. J Biol Chem, 274: 2556–62.

    PubMed  CAS  Google Scholar 

  • Piskin, S., Saygin, A., Doganay, L., Kircuval, D., and Gurkan, E., 2004, Coexistence of Darier’s disease and acrokeratosis verruciformis of Hopf. Yonsei Med J, 45: 956–9.

    PubMed  Google Scholar 

  • Prakriya, M., Feske, S., Gwack, Y., Srikanth, S., Rao, A., and Hogan, P. G., 2006, Orai1 is an essential pore subunit of the CRAC channel. Nature, 443: 230–3.

    PubMed  CAS  Google Scholar 

  • Prasad, V., Boivin, G. P., Miller, M. L., Liu, L. H., Erwin, C. R., Warner, B. W., and Shull, G. E., 2005, Haploinsufficiency of Atp2a2, encoding the sarco(endo)plasmic reticulum Ca2+-ATPase isoform 2 Ca2+ pump, predisposes mice to squamous cell tumors via a novel mode of cancer susceptibility. Cancer Res, 65: 8655–61.

    PubMed  CAS  Google Scholar 

  • Prasad, V., Okunade, G. W., Miller, M. L., and Shull, G. E., 2004, Phenotypes of SERCA and PMCA knockout mice. Biochem Biophys Res Commun, 322: 1192–203.

    PubMed  CAS  Google Scholar 

  • Racz, E., Csikos, M., Benko, R., Kornsee, Z., and Karpati, S., 2005, Three novel mutations in the ATP2A2 gene in Hungarian families with Darier’s disease, including a novel splice site generating intronic nucleotide change. J Dermatol Sci, 38: 231–4.

    PubMed  CAS  Google Scholar 

  • Racz, E., Csikos, M., Kornsee, Z., Horvath, A., and Karpati, S., 2004, Identification of mutations in the ATP2A2 gene in patients with Darier’s disease from Hungary. Exp Dermatol, 13: 396–9.

    PubMed  CAS  Google Scholar 

  • Rallis, E., Economidi, A., Papadakis, P., and Verros, C., 2005, Acrokeratosis verruciformis of Hopf (Hopf disease): case report and review of the literature. Dermatol Online J, 11: 10.

    PubMed  CAS  Google Scholar 

  • Reese, D. A., Paul, A. Y., and Davis, B., 2005, Unilateral segmental Darier disease following Blaschko lines: a case report and review of the literature. Cutis, 76: 197–200.

    PubMed  Google Scholar 

  • Ren, Y. Q., Gao, M., Liang, Y. H., Hou, Y. X., Wang, P. G., Sun, L. D., Xu, S. X., Li, W., Du, W. H., Zhou, F. S., Shen, Y. J., Yang, S., and Zhang, X. J., 2006, Five mutations of ATP2A2 gene in Chinese patients with Darier’s disease and a literature review of 86 cases reported in China. Arch Dermatol Res, 298: 58–63.

    PubMed  CAS  Google Scholar 

  • Ringpfeil, F., Raus, A., DiGiovanna, J. J., Korge, B., Harth, W., Mazzanti, C., Uitto, J., Bale, S. J., and Richard, G., 2001, Darier disease–novel mutations in ATP2A2 and genotype-phenotype correlation. Exp Dermatol, 10: 19–27.

    PubMed  CAS  Google Scholar 

  • Roderick, H. L., Lechleiter, J. D., and Camacho, P., 2000, Cytosolic phosphorylation of calnexin controls intracellular Ca(2+) oscillations via an interaction with SERCA2b. J Cell Biol, 149: 1235–48.

    PubMed  CAS  Google Scholar 

  • Rossi, A. E., and Dirksen, R. T., 2006, Sarcoplasmic reticulum: the dynamic calcium governor of muscle. Muscle Nerve, 33: 715–31.

    PubMed  CAS  Google Scholar 

  • Rubegni, P., Poggiali, S., Sbano, P., Risulo, M., and Fimiani, M., 2006, A case of Darier’s disease successfully treated with topical tacrolimus. J Eur Acad Dermatol Venereol, 20: 84–7.

    PubMed  CAS  Google Scholar 

  • Ruiz-Perez, V. L., Carter, S. A., Healy, E., Todd, C., Rees, J. L., Steijlen, P. M., Carmichael, A. J., Lewis, H. M., Hohl, D., Itin, P., Vahlquist, A., Gobello, T., Mazzanti, C., Reggazini, R., Nagy, G., Munro, C. S., and Strachan, T., 1999, ATP2A2 mutations in Darier’s disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class. Hum Mol Genet, 8: 1621–30.

    PubMed  CAS  Google Scholar 

  • Sakuntabhai, A., Burge, S., Monk, S., and Hovnanian, A., 1999a, Spectrum of novel ATP2A2 mutations in patients with Darier’s disease. Hum Mol Genet, 8: 1611–9.

    PubMed  CAS  Google Scholar 

  • Sakuntabhai, A., Dhitavat, J., Burge, S., and Hovnanian, A., 2000, Mosaicism for ATP2A2 mutations causes segmental Darier’s disease. J Invest Dermatol, 115: 1144–7.

    PubMed  CAS  Google Scholar 

  • Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C. S., O’Donovan, M., Craddock, N., Kucherlapati, R., Rees, J. L., Owen, M., Lathrop, G. M., Monaco, A. P., Strachan, T., and Hovnanian, A., 1999, b, Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nat Genet, 21: 271–7.

    PubMed  CAS  Google Scholar 

  • Schueller, W. A., 1972, Acrokeratosis verruciformis of Hopf. Arch Dermatol, 106: 81–3.

    PubMed  CAS  Google Scholar 

  • Shull, G. E., Okunade, G., Liu, L. H., Kozel, P., Periasamy, M., Lorenz, J. N., and Prasad, V., 2003, Physiological functions of plasma membrane and intracellular Ca2+ pumps revealed by analysis of null mutants. Ann N Y Acad Sci, 986: 453–60.

    PubMed  CAS  Google Scholar 

  • Strehler, E. E., and Treiman, M., 2004, Calcium pumps of plasma membrane and cell interior. Curr Mol Med, 4: 323–35.

    PubMed  CAS  Google Scholar 

  • Sudbrak, R., Brown, J., Dobson-Stone, C., Carter, S., Ramser, J., White, J., Healy, E., Dissanayake, M., Larregue, M., Perrussel, M., Lehrach, H., Munro, C. S., Strachan, T., Burge, S., Hovnanian, A., and Monaco, A. P., 2000, Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump. Hum Mol Genet, 9: 1131–40.

    PubMed  CAS  Google Scholar 

  • Sumbilla, C., Cavagna, M., Zhong, L., Ma, H., Lewis, D., Farrance, I., and Inesi, G., 1999, Comparison of SERCA1 and SERCA2a expressed in COS-1 cells and cardiac myocytes. Am J Physiol, 277: H2381–91.

    PubMed  CAS  Google Scholar 

  • Svendsen, I. B., and Albrecten, B., 1959, The prevalence of dyskeratosis follicularis (Darier’s disease) in Danemark. Acta Derm Venereol, 39: 256–69.

    PubMed  CAS  Google Scholar 

  • Takahashi, H., Atsuta, Y., Sato, K., Ishida-Yamamoto, A., Suzuki, H., and Iizuka, H., 2001, Novel mutations of ATP2A2 gene in Japanese patients of Darier’s disease. J Dermatol Sci, 26: 169–72.

    PubMed  CAS  Google Scholar 

  • Tavadia, S., Authi, K. S., Hodgins, M. B., and Munro, C. S., 2004, Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier’s disease. Br J Dermatol, 151: 440–5.

    PubMed  CAS  Google Scholar 

  • Tavadia, S., Mortimer, E., and Munro, C. S., 2002, Genetic epidemiology of Darier’s disease: a population study in the west of Scotland. Br J Dermatol, 146: 107–9.

    PubMed  CAS  Google Scholar 

  • Tavadia, S., Tait, R. C., McDonagh, T. A., and Munro, C. S., 2001, Platelet and cardiac function in Darier’s disease. Clin Exp Dermatol, 26: 696–9.

    PubMed  CAS  Google Scholar 

  • Toyoshima, C., and Inesi, G., 2004, Structural basis of ion pumping by Ca2+-ATPase of the sarcoplasmic reticulum. Annu Rev Biochem, 73: 269–92.

    PubMed  CAS  Google Scholar 

  • Toyoshima, C., Nakasako, M., Nomura, H., and Ogawa, H., 2000, Crystal structure of the calcium pump of sarcoplasmic reticulum at 2.6 A resolution. Nature, 405: 647–55.

    PubMed  CAS  Google Scholar 

  • Toyoshima, C., Nomura, H., and Sugita, Y., 2003, Crystal structures of Ca2+-ATPase in various physiological states. Ann N Y Acad Sci, 986: 1–8.

    PubMed  CAS  Google Scholar 

  • Vangheluwe, P., Raeymaekers, L., Dode, L., and Wuytack, F., 2005, Modulating sarco(endo)plasmic reticulum Ca(2+) ATPase 2 (SERCA2) activity: cell biological implications. Cell Calcium, 38: 291–302.

    PubMed  CAS  Google Scholar 

  • Varadi, A., Lebel, L., Hashim, Y., Mehta, Z., Ashcroft, S. J., and Turner, R., 1999, Sequence variants of the sarco(endo)plasmic reticulum Ca(2+)-transport ATPase 3 gene (SERCA3) in Caucasian type II diabetic patients (UK Prospective Diabetes Study 48). Diabetologia, 42: 1240–3.

    PubMed  CAS  Google Scholar 

  • Ver Heyen, M., Heymans, S., Antoons, G., Reed, T., Periasamy, M., Awede, B., Lebacq, J., Vangheluwe, P., Dewerchin, M., Collen, D., Sipido, K., Carmeliet, P., and Wuytack, F., 2001, Replacement of the muscle-specific sarcoplasmic reticulum Ca(2+)-ATPase isoform SERCA2a by the nonmuscle SERCA2b homologue causes mild concentric hypertrophy and impairs contraction-relaxation of the heart. Circ Res, 89: 838–46.

    PubMed  CAS  Google Scholar 

  • Verboomen, H., Wuytack, F., De Smedt, H., Himpens, B., and Casteels, R., 1992, Functional difference between SERCA2a and SERCA2b Ca2+ pumps and their modulation by phospholamban. Biochem J, 286 (Pt 2): 591–5.

    PubMed  CAS  Google Scholar 

  • Verboomen, H., Wuytack, F., Van den Bosch, L., Mertens, L., and Casteels, R., 1994, The functional importance of the extreme C-terminal tail in the gene 2 organellar Ca2+-transport ATPase (SERCA2a/b). Biochem J, 303 (Pt 3): 979–84.

    PubMed  CAS  Google Scholar 

  • Wada, T., Shirakata, Y., Takahashi, H., Murakami, S., Iizuka, H., Suzuki, H., and Hashimoto, K., 2003, A Japanese case of segmental Darier’s disease caused by mosaicism for the ATP2A2 mutation. Br J Dermatol, 149: 185–8.

    PubMed  CAS  Google Scholar 

  • Waisman, M., 1960, Verruciform manifestations of keratosis follicularis. Arch. Dermatol., 81: 1–14.

    Google Scholar 

  • Wang, P. G., Gao, M., Lin, G. S., Yang, S., Lin, D., Liang, Y. H., Zhang, G. L., Zhu, Y. G., Cui, Y., Zhang, K. Y., Huang, W., and Zhang, X. J., 2006, Genetic heterogeneity in acrokeratosis verruciformis of Hopf. Clin Exp Dermatol, 31: 558–63.

    PubMed  Google Scholar 

  • Wilkinson, J. D., 1977, Orf: a family with unusual complications. Br J Dermatol, 97: 447–50.

    PubMed  CAS  Google Scholar 

  • Wuytack, F., Dode, L., Baba-Aissa, F., and Raeymaekers, L., 1995, The SERCA3-type of organellar Ca2+ pumps. Biosci Rep, 15: 299–306.

    PubMed  CAS  Google Scholar 

  • Wuytack, F., Raeymaekers, L., and Missiaen, L., 2002, Molecular physiology of the SERCA and SPCA pumps. Cell Calcium, 32: 279–305.

    PubMed  CAS  Google Scholar 

  • Yang, Y., Li, G., Bu, D., and Zhu, X., 2001, Novel point mutations of the ATP2A2 gene in two Chinese families with Darier disease. J Invest Dermatol, 116: 482–3.

    PubMed  CAS  Google Scholar 

  • Zhang, Y., Fujii, J., Phillips, M. S., Chen, H. S., Karpati, G., Yee, W. C., Schrank, B., Cornblath, D. R., Boylan, K. B., and MacLennan, D. H., 1995, Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease. Genomics, 30: 415–24.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2007 Springer

About this chapter

Cite this chapter

HOVNANIAN, A. (2007). Serca pumps and human diseases. In: Carafoli, E., Brini, M. (eds) Calcium Signalling and Disease. Subcellular Biochemistry, vol 45. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-6191-2_12

Download citation

Publish with us

Policies and ethics