Abstract
The characterization of a novel 59-kD cytoskeletal protein is described. It is exclusively observed in smooth muscle cells by Northern blotting and immunohistochemical analysis and therefore designated "smoothelin." A human smooth muscle cDNA library was screened with the monoclonal antibody R4A, and a full-size cDNA of the protein was selected. The cDNA was sequenced and appeared to contain a 1,113-bp open reading frame. Based on the cDNA sequence, the calculated molecular weight of the polypeptide was 40 kD and it was demonstrated to contain two N-glycosylation sites. Computer assisted analysis at the protein level revealed a 56-amino acid domain with homologies of approximately 40% with a sequence bordering the actin-binding domains of dystrophin, utrophin, beta-spectrin and alpha-actinin. In situ hybridization demonstrated that human smoothelin is encoded by a single copy gene which is located on chromosome 22. Immunohistochemistry and Western blotting revealed synthesis of smoothelin in smooth muscle of species evolutionarily as far apart as human and teleost. Northern blotting indicated that sequence as well as size of the mRNA (approximately 1,500 bases) are conserved among vertebrates. Cell fractionation studies and differential centrifugation showed that the protein cannot be extracted with Triton X-100, which indicates that it is a part of the cytoskeleton. Transfection of the human cDNA into smooth muscle cells and COS7 cells produced a protein of 59 kD, which assembled into a filamentous network. However, in rat heart-derived myoblasts association with stress fibers was most prominent. Smoothelin was not detected in primary or long term smooth muscle cell cultures. Also, transcription of smoothelin mRNA was almost instantly halted in smooth muscle tissue explants. We conclude that smoothelin is a new cytoskeletal protein that is only found in contractile smooth muscle cells and does not belong to one of the classes of structural proteins presently known.
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- Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
- Auffray C., Rougeon F. Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA. Eur J Biochem. 1980 Jun;107(2):303–314. doi: 10.1111/j.1432-1033.1980.tb06030.x. [DOI] [PubMed] [Google Scholar]
- Aviv H., Leder P. Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1408–1412. doi: 10.1073/pnas.69.6.1408. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Babai F., Musevi-Aghdam J., Schurch W., Royal A., Gabbiani G. Coexpression of alpha-sarcomeric actin, alpha-smooth muscle actin and desmin during myogenesis in rat and mouse embryos I. Skeletal muscle. Differentiation. 1990 Aug;44(2):132–142. doi: 10.1111/j.1432-0436.1990.tb00546.x. [DOI] [PubMed] [Google Scholar]
- Baron M. D., Davison M. D., Jones P., Critchley D. R. The sequence of chick alpha-actinin reveals homologies to spectrin and calmodulin. J Biol Chem. 1987 Dec 25;262(36):17623–17629. [PubMed] [Google Scholar]
- Beggs A. H., Byers T. J., Knoll J. H., Boyce F. M., Bruns G. A., Kunkel L. M. Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11. J Biol Chem. 1992 May 5;267(13):9281–9288. [PubMed] [Google Scholar]
- Berbers G. A., Hoekman W. A., Bloemendal H., de Jong W. W., Kleinschmidt T., Braunitzer G. Proline- and alanine-rich N-terminal extension of the basic bovine beta-crystallin B1 chains. FEBS Lett. 1983 Sep 19;161(2):225–229. doi: 10.1016/0014-5793(83)81013-8. [DOI] [PubMed] [Google Scholar]
- Borrione A. C., Zanellato A. M., Giuriato L., Scannapieco G., Pauletto P., Sartore S. Nonmuscle and smooth muscle myosin isoforms in bovine endothelial cells. Exp Cell Res. 1990 Sep;190(1):1–10. doi: 10.1016/0014-4827(90)90136-x. [DOI] [PubMed] [Google Scholar]
- Campbell G. R., Chamley-Campbell J. H. Smooth muscle phenotypic modulation: role in atherogenesis. Med Hypotheses. 1981 Jun;7(6):729–735. doi: 10.1016/0306-9877(81)90084-0. [DOI] [PubMed] [Google Scholar]
- Campbell J. H., Kocher O., Skalli O., Gabbiani G., Campbell G. R. Cytodifferentiation and expression of alpha-smooth muscle actin mRNA and protein during primary culture of aortic smooth muscle cells. Correlation with cell density and proliferative state. Arteriosclerosis. 1989 Sep-Oct;9(5):633–643. doi: 10.1161/01.atv.9.5.633. [DOI] [PubMed] [Google Scholar]
- Church G. M., Gilbert W. Genomic sequencing. Proc Natl Acad Sci U S A. 1984 Apr;81(7):1991–1995. doi: 10.1073/pnas.81.7.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dhermy D. The spectrin super-family. Biol Cell. 1991;71(3):249–254. [PubMed] [Google Scholar]
- Duband J. L., Gimona M., Scatena M., Sartore S., Small J. V. Calponin and SM 22 as differentiation markers of smooth muscle: spatiotemporal distribution during avian embryonic development. Differentiation. 1993 Dec;55(1):1–11. doi: 10.1111/j.1432-0436.1993.tb00027.x. [DOI] [PubMed] [Google Scholar]
- Frid M. G., Shekhonin B. V., Koteliansky V. E., Glukhova M. A. Phenotypic changes of human smooth muscle cells during development: late expression of heavy caldesmon and calponin. Dev Biol. 1992 Oct;153(2):185–193. doi: 10.1016/0012-1606(92)90104-o. [DOI] [PubMed] [Google Scholar]
- Gabbiani G., Schmid E., Winter S., Chaponnier C., de Ckhastonay C., Vandekerckhove J., Weber K., Franke W. W. Vascular smooth muscle cells differ from other smooth muscle cells: predominance of vimentin filaments and a specific alpha-type actin. Proc Natl Acad Sci U S A. 1981 Jan;78(1):298–302. doi: 10.1073/pnas.78.1.298. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glukhova M. A., Kabakov A. E., Belkin A. M., Frid M. G., Ornatsky O. I., Zhidkova N. I., Koteliansky V. E. Meta-vinculin distribution in adult human tissues and cultured cells. FEBS Lett. 1986 Oct 20;207(1):139–141. doi: 10.1016/0014-5793(86)80027-8. [DOI] [PubMed] [Google Scholar]
- Gluzman Y. SV40-transformed simian cells support the replication of early SV40 mutants. Cell. 1981 Jan;23(1):175–182. doi: 10.1016/0092-8674(81)90282-8. [DOI] [PubMed] [Google Scholar]
- Gunning P., Gordon M., Wade R., Gahlmann R., Lin C. S., Hardeman E. Differential control of tropomyosin mRNA levels during myogenesis suggests the existence of an isoform competition-autoregulatory compensation control mechanism. Dev Biol. 1990 Apr;138(2):443–453. doi: 10.1016/0012-1606(90)90210-a. [DOI] [PubMed] [Google Scholar]
- Haeberle J. R., Hathaway D. R., Smith C. L. Caldesmon content of mammalian smooth muscles. J Muscle Res Cell Motil. 1992 Feb;13(1):81–89. doi: 10.1007/BF01738431. [DOI] [PubMed] [Google Scholar]
- Karinch A. M., Zimmer W. E., Goodman S. R. The identification and sequence of the actin-binding domain of human red blood cell beta-spectrin. J Biol Chem. 1990 Jul 15;265(20):11833–11840. [PubMed] [Google Scholar]
- Kimes B. W., Brandt B. L. Properties of a clonal muscle cell line from rat heart. Exp Cell Res. 1976 Mar 15;98(2):367–381. doi: 10.1016/0014-4827(76)90447-x. [DOI] [PubMed] [Google Scholar]
- Koenig M., Monaco A. P., Kunkel L. M. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell. 1988 Apr 22;53(2):219–228. doi: 10.1016/0092-8674(88)90383-2. [DOI] [PubMed] [Google Scholar]
- Köhler G., Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature. 1975 Aug 7;256(5517):495–497. doi: 10.1038/256495a0. [DOI] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lees-Miller J. P., Heeley D. H., Smillie L. B. An abundant and novel protein of 22 kDa (SM22) is widely distributed in smooth muscles. Purification from bovine aorta. Biochem J. 1987 Jun 15;244(3):705–709. doi: 10.1042/bj2440705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McHugh K. M., Crawford K., Lessard J. L. A comprehensive analysis of the developmental and tissue-specific expression of the isoactin multigene family in the rat. Dev Biol. 1991 Dec;148(2):442–458. doi: 10.1016/0012-1606(91)90263-3. [DOI] [PubMed] [Google Scholar]
- Nagai R., Kuro-o M., Babij P., Periasamy M. Identification of two types of smooth muscle myosin heavy chain isoforms by cDNA cloning and immunoblot analysis. J Biol Chem. 1989 Jun 15;264(17):9734–9737. [PubMed] [Google Scholar]
- Nanaev A. K., Shirinsky V. P., Birukov K. G. Immunofluorescent study of heterogeneity in smooth muscle cells of human fetal vessels using antibodies to myosin, desmin, and vimentin. Cell Tissue Res. 1991 Dec;266(3):535–540. doi: 10.1007/BF00318595. [DOI] [PubMed] [Google Scholar]
- O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
- Owens G. K. Regulation of differentiation of vascular smooth muscle cells. Physiol Rev. 1995 Jul;75(3):487–517. doi: 10.1152/physrev.1995.75.3.487. [DOI] [PubMed] [Google Scholar]
- Pless D. D., Lennarz W. J. Enzymatic conversion of proteins to glycoproteins. Proc Natl Acad Sci U S A. 1977 Jan;74(1):134–138. doi: 10.1073/pnas.74.1.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Quax-Jeuken Y. E., Quax W. J., Bloemendal H. Primary and secondary structure of hamster vimentin predicted from the nucleotide sequence. Proc Natl Acad Sci U S A. 1983 Jun;80(12):3548–3552. doi: 10.1073/pnas.80.12.3548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ramaekers F. C., Moesker O., Huysmans A., Schaart G., Westerhof G., Wagenaar S. S., Herman C. J., Vooijs G. P. Intermediate filament proteins in the study of tumor heterogeneity: an in-depth study of tumors of the urinary and respiratory tracts. Ann N Y Acad Sci. 1985;455:614–634. doi: 10.1111/j.1749-6632.1985.tb50440.x. [DOI] [PubMed] [Google Scholar]
- Ramaekers F. C., Puts J. J., Moesker O., Kant A., Huysmans A., Haag D., Jap P. H., Herman C. J., Vooijs G. P. Antibodies to intermediate filament proteins in the immunohistochemical identification of human tumours: an overview. Histochem J. 1983 Jul;15(7):691–713. doi: 10.1007/BF01002988. [DOI] [PubMed] [Google Scholar]
- Rost B., Sander C. Combining evolutionary information and neural networks to predict protein secondary structure. Proteins. 1994 May;19(1):55–72. doi: 10.1002/prot.340190108. [DOI] [PubMed] [Google Scholar]
- Rost B., Sander C. Prediction of protein secondary structure at better than 70% accuracy. J Mol Biol. 1993 Jul 20;232(2):584–599. doi: 10.1006/jmbi.1993.1413. [DOI] [PubMed] [Google Scholar]
- Sanger F., Coulson A. R., Barrell B. G., Smith A. J., Roe B. A. Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing. J Mol Biol. 1980 Oct 25;143(2):161–178. doi: 10.1016/0022-2836(80)90196-5. [DOI] [PubMed] [Google Scholar]
- Schaart G., Pieper F. R., Kuijpers H. J., Bloemendal H., Ramaekers F. C. Baby hamster kidney (BHK-21/C13) cells can express striated muscle type proteins. Differentiation. 1991 Mar;46(2):105–115. doi: 10.1111/j.1432-0436.1991.tb00871.x. [DOI] [PubMed] [Google Scholar]
- Skalli O., Ropraz P., Trzeciak A., Benzonana G., Gillessen D., Gabbiani G. A monoclonal antibody against alpha-smooth muscle actin: a new probe for smooth muscle differentiation. J Cell Biol. 1986 Dec;103(6 Pt 2):2787–2796. doi: 10.1083/jcb.103.6.2787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takahashi K., Hiwada K., Kokubu T. Vascular smooth muscle calponin. A novel troponin T-like protein. Hypertension. 1988 Jun;11(6 Pt 2):620–626. doi: 10.1161/01.hyp.11.6.620. [DOI] [PubMed] [Google Scholar]
- Takeuchi K., Takahashi K., Abe M., Nishida W., Hiwada K., Nabeya T., Maruyama K. Co-localization of immunoreactive forms of calponin with actin cytoskeleton in platelets, fibroblasts, and vascular smooth muscle. J Biochem. 1991 Feb;109(2):311–316. [PubMed] [Google Scholar]
- Tinsley J. M., Blake D. J., Roche A., Fairbrother U., Riss J., Byth B. C., Knight A. E., Kendrick-Jones J., Suthers G. K., Love D. R. Primary structure of dystrophin-related protein. Nature. 1992 Dec 10;360(6404):591–593. doi: 10.1038/360591a0. [DOI] [PubMed] [Google Scholar]
- Turner C. E., Burridge K. Detection of metavinculin in human platelets using a modified talin overlay assay. Eur J Cell Biol. 1989 Jun;49(1):202–206. [PubMed] [Google Scholar]
- Vaughan K. T., Weber F. E., Einheber S., Fischman D. A. Molecular cloning of chicken myosin-binding protein (MyBP) H (86-kDa protein) reveals extensive homology with MyBP-C (C-protein) with conserved immunoglobulin C2 and fibronectin type III motifs. J Biol Chem. 1993 Feb 15;268(5):3670–3676. [PubMed] [Google Scholar]
- Voorter C., Joos S., Bringuier P. P., Vallinga M., Poddighe P., Schalken J., du Manoir S., Ramaekers F., Lichter P., Hopman A. Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization. Am J Pathol. 1995 Jun;146(6):1341–1354. [PMC free article] [PubMed] [Google Scholar]
- Winder S. J., Hemmings L., Maciver S. K., Bolton S. J., Tinsley J. M., Davies K. E., Critchley D. R., Kendrick-Jones J. Utrophin actin binding domain: analysis of actin binding and cellular targeting. J Cell Sci. 1995 Jan;108(Pt 1):63–71. doi: 10.1242/jcs.108.1.63. [DOI] [PubMed] [Google Scholar]
- Winkelmann J. C., Chang J. G., Tse W. T., Scarpa A. L., Marchesi V. T., Forget B. G. Full-length sequence of the cDNA for human erythroid beta-spectrin. J Biol Chem. 1990 Jul 15;265(20):11827–11832. [PubMed] [Google Scholar]
