Transglutaminases in skin biology

Minerva Biotecnologica

Volumn 14, Issue 2, 2002, Pages 165-169

  Ahvazi, B ^a   Boeshans, K ^a   Jang, S I ^a   Kalinin, A E ^a   Steinert, P M ^a  

^a NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

Author keywords

Protein glutamine gamma glutamyltransferase, genetics; Protein glutamine gamma glutamyltransferase, physiopathology; Skin

Indexed keywords

PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; STRUCTURAL PROTEIN;

ARTICLE; BIOCHEMISTRY; CELL DIFFERENTIATION; CELL MEMBRANE; CELL STRUCTURE; CELL SURVIVAL; CONTROLLED STUDY; EPITHELIUM CELL; GENE ACTIVITY; GENE EXPRESSION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HUMAN GENOME; HUMAN TISSUE; KERATINOCYTE; MATURATION; MOLECULAR BIOLOGY; PERMEABILITY BARRIER; PROTEIN CROSS LINKING; PROTEIN FAMILY; SKIN; SQUAMOUS EPITHELIUM;

EID: 0036621817     PISSN: 11204826     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. Grenard P, Bates MK, Aeschlimann D. Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase Z. J Biol Chem 2001;276:33066-78.
2. Steinert PM, Marekov LN. Initiation of assembly of the cell envelope barrier structure of stratified squamous epithelia. Mol Biol Cell 1999;10:4247-61.
3. Kalinin A, Marekov LN, Steinert PM. Assembly of the epidermal cornified cell envelope. J Cell Sci 2001;117:3069-70.
4. Jarnik M, Simon MN, Steven AC. Cornified cell envelope assembly: a model based on electron microscopic determinations of thickness and projected density. J Cell Sci 1998;111:1051-60.
5. Nemes Z, Marekov LN, Fesus L, Steinert PM. A novel function for the transglutaminase 1 enzyme: attachment of long chain ω-hydroxyceramides to involucrin by ester bond formation. Proc Natl Acad Sci USA 1999;96:8402-7.
6. Kim H-C, Lewis MS, Gorman JJ, Park SC, Girard JE, Folk JE et al. Protransglutaminase E from guinea pig skin. Isolation and partial characterization. J Biol Chem 1990;265:21971-8.
7. Kim S-Y, Chung S-I, Steinert PM. Highly active soluble processed forms of the transglutaminase 1 enzyme in epidermal keratinocytes. J Biol Chem 1995;270:18026-35.
8. Candi E, Melino G, Pei G, Tarcsa E, Marekov LN, Steinert PM. Bacterially-expressed human loricrin: Biochemical, structural and- transglutaminase substrate properties of the major epidermal cornified cell envelope structural protein. J Biol Chem 1995;270:26382-90.
9. Candi E, Tarcsa E, Kartasova T, Idler WW, Marekov LN, Steinert PM. Biochemical and transglutaminase substrate properties of the small proline rich 1 family of cornified cell envelope proteins: integration with loricrin. J Biol Chem 1999;274:7226-37.
10. Tarcsa E, Candi E, Kartasova T, Idler WW, Marekov LN, Steinert PM. Structural and transglutaminase substrate properties of the small proline rich 2 family of cornified cell envelope proteins. J Biol Chem 1998;273:23297-303.
11. Steinert PM, Candi E, Tarcsa E, Marekov LN, Sette M, Paci M et al. Transglutaminase crosslinking and structural studies of the human small proline rich 3 protein. Cell Death Differ 1999;6:916-30.
12. Tarcsa E, Marekov LN, Andreoli JM, Idler WW, Candi E, Chung S-I et al. The fate of trichohyalin: sequential post-translational modifications by peptidylarginine deiminase and transglutaminases. J Biol Chem 1997;272:27893-901.
13. Folk JE, Chung S-I. Transglutaminases. Methods Enzymol 1985;113:358-75.
14. Kim SY, Jeitner TM, Steinert PM. Transglutaminases in disease. Neurochem Int 2002;40:85-103.
15. Ahvazi B, Kim H-C, Nemes Z, Steinert PM. Three-dimension structure of the human transglutaminase 3 enzyme: three calcium ions are required for activity. EMBO J 2002;21:2055-67.
16. De Laurenzi V, Melino G. Gene disruption of tissue transglutaminase. Mol Cell Biol 2001;21:148-55.
17. Nanda N, Iismaa SE, Owens WA, Husain A, Mackay F, Graham RM. Targeted inactivation of Gh/tissue transglutaminase II. J Biol Chem 2001;276:20673-8.
18. Traupe H. Isolated congenital ichthyoses. In: Traupe H, editors. The Ichthyoses. A Guide to Clinical Diagnosis, Genetic Counseling and Therapy. Berlin: Springer; 1989.p.103-54.
19. Russell LJ, DiGiovanna JJ, Hashem N, Rogers GR, Steinert PM, Compton JG et al. TGM1 mutations in lamellar ichthyosis. Nat Genet 1995;9:279-83.
20. Yang J-M, Alm K-S, Cho M-O, Yoneda K, Park K-B, Lee E-S et al. Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis. J Invest Dermatol 2001;117:214-8.
21. Matsuki M, Yamashita F, Ishida-Yamamoto A, Yamada K, Kinoshita C, Fushiki S et al. Proc Natl Acad Sci USA 1998;95:1044-9.
22. Epstein EH, Williams ML, Elias PM. J Am Acad Dermatol 1984;10:866-8.
23. Nemes Z, Demeny MA, Marekov LN, Fesus L, Steinert PM. Cholesterol-3-sulfate interferes with cornified envelope assembly by diverting transglutaminase 1 activity from the formation of crosslinks and esters to hydrolysis of glutamines. J Biol Chem 2000;275:2636-46.
24. De Laurenzi V, Markova NG, Rogers GR, Steinert PM, Marekov LN, Compton JG et al. Sjögren-Larsson Syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene. Nat Genet 1996;21:2-7.
25. Raghunath M, Hennies H-C, Vogel M, Hamm H, Ergezinger K, Steinert PM et al. The self-healing collodion baby - an allelic variant of transglutaminase 1-deficient lamellar ichthyosis? J Invest Dermatol. In press 2002.