Farnesylation of Batten disease CLN3 protein

Neuropediatrics

Volumn 28, Issue 1, 1997, Pages 42-44

  Pullarkat, Raju K ^a   Morris, George N ^a  

^a NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES   (United States)

Author keywords

Batten disease; Farnesylation; Neuronal ceroid lipofuscinosis

Indexed keywords

CYSTEINE; GENE PRODUCT; PROTEIN; TETRAPEPTIDE; TRANSFERASE;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; BRAIN; CARBOXY TERMINAL SEQUENCE; CATTLE; FARNESYLATION; NEURONAL CEROID LIPOFUSCINOSIS; NONHUMAN; PRENYLATION; PRIORITY JOURNAL;

EID: 0030786568     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973665     Document Type: Article

References (17)

1. Batten Disease Consortium: Isolation of a novel gene underlying Batten disease, CLN3. Cell 82 (1995) 949-957
2. Belard, M., R. Cacan, A. Verbert: Characterization of an oligosaccharide-pyrophosphodolichol pyrophosphatase activity in yeast. Biochem. J. 255 (1988) 235-242
3. Clarke, S.: Protein isoprenylation and methylation at carboxyl-terminal cysteine residues. Ann Rev. Biochem. 61 (1992) 355-386
4. Faisal, K. M., S. Sklower Brooks, R. K. Pullarkat: Abnormal acid phosphatases in neuronal ceroid-lipofuscinoses. Am. J. Med. Genet. 57 (1995) 285-289
5. Hall, N. A., A. D. Patrick: Accumulation of dolichol-linked oligosaccharides in ceroid lipofuscinosis (Batten disease). Am J. Med. Genet. (Suppl) 5 (1988) 221-232
6. Johnson, D. R., R. S. Bhatnagar, L. J. Knoll, J. I. Gordon: Genetic and biochemical studies of protein N-myristoylation. Annu. Rev. Biochem. 63 (1994) 869-914
7. Kaczmarski, W., E. Kida, A. Lach, R. Rubenstein, N. Zong, K. E. Wisniewski: Expression studies of CLN3 protein. Sixth Internatl. Cong. on Neuronal Ceroid-Lipofuscinoses. Abstract 30.
8. Kamiya, Y., A. Saurai, S. Tamara, N. Takahashi, E. Tscuhiya, K. Abe, S. Fukui: Structure of rhodotorucine, a peptide factor, inducing mating tube formation in Rhodporidum toruloides. Agri. Biol. Chem. 43 (1979) 363-369
9. Kawata, M., C. C. Farnsworth, Y. Yoshida, M. H. Geld, J. A. Glomset, Y. Takai: Posttranslationally processed structure of the human platelet protein smg p21B: Evidence for geranylgeranylation and carboxyl methylation of the cysteine residue. Proc. Natl. Acad. Sci. USA 87 (1990) 8960-8964
10. Moores, S. L., M. D. Schaber, S. D. Mosser, E. Rands, M. B. O'Hara, V. M. Garsky, M. S. Marshall, D. L. Pompliano, J. B. Gibbs: Sequence dependence of protein isoprenylation. J. Biol. Chem. 266 (1991) 14603-14610
11. Morris, G. N., R. K. Pullarkat: Bovine brain gray and white matter exhibit differential protein prenyl transferase activity. Neurochem. Res. 20 (1995) 457-460
12. Munroe, P. B., J. Rapola, H. M. Mitchison, A. Mustonen, S. E. Mole, R. M. Gardiner, I Jarvela: Prenatal diagnosis of Batten's disease. Lancet 347 (1996) 1014-1015
13. Pullarkat, R. K., K. S. Kim, S. L. Sklower, V. K. Patel: Oligosaccharyl diphosphodolichol in the ceroid-lipofuscinoses. Am. J. Med Genet. (suppl) 5 (1988) 243-251
14. Sepp-Lorenzino, L., P. S. Coleman, J. N. Larocca: Isoprenylated proteins in myelin. J. Neurochem. 62 (1994) 1539-1545
15. Reiss, Y., M. C. Seabra, J L. Goldstein, M. S. Brown: Purification of ras farnesyl: protein transferase. Meth. Compan. Meth Enzymol 1 (1990) 241-245
16. Wisniewski, K. E., E. Kida, O Patxot, F. Connel: Variability in the clinical and pathological findings in the neuronal ceroid lipofuscinoses: Review of literature and observations. Am. J Med Genet. 42 (1992) 525-532
17. Zeman, W., S. Donahue, P. Dyken, J. Green: The Neuronal Ceroid-lipofuscinoses (Batten-Vogt syndrome). In: Handbook of Neurology vol. 10, edited by P. J. Vinkin, G. W. Bruyn. Amsterdam, Elsevier (1970) 558-659