ISOLATION, CHARACTERIZATION, AND EXPRESSION OF CDNA CLONES THAT ENCODE RAT UDP-GALACTOSE - CERAMIDE GALACTOSYLTRANSFERASE

被引:92
作者
STAHL, N
JUREVICS, H
MORELL, P
SUZUKI, K
POPKO, B
机构
[1] UNIV N CAROLINA, BRAIN & DEV RES CTR, CHAPEL HILL, NC 27599 USA
[2] UNIV N CAROLINA, DEPT BIOCHEM & BIOPHYS, CHAPEL HILL, NC USA
[3] UNIV N CAROLINA, PROGRAM MOLEC BIOL & BIOTECHNOL, CHAPEL HILL, NC 27599 USA
[4] UNIV N CAROLINA, DEPT NEUROL & PSYCHIAT, CHAPEL HILL, NC USA
关键词
GALACTOCEREBROSIDE; NERVE REGENERATION; OLIGODENDROCYTES; SCHWANN CELLS; DEVELOPMENT; MYELIN;
D O I
10.1002/jnr.490380214
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
UDP-galactose:ceramide galactosyltransferase (CGT) (EC. 2.4.1.62) catalyzes the final step in the synthesis of galactocerebroside (GalC), a glycosphingolipid found in high amounts in the myelin sheath. Here, the isolation of rat CGT specific cDNA clones is reported. The CGT sequence contains an open reading frame of 1,623 bp which predicts a protein of M(r) 61,126 Da. In transfection experiments the cDNA was found to confer CGT activity to Chinese hamster ovary cells. In rat brain the developmental expression pattern of CGT mRNA was similar to the myelination profile, whereas the sciatic nerve contained high amounts of CGT message over a long developmental period. CGT mRNA expression in the sciatic nerve was found to drop substantially following nerve injury and recover slowly when compared to the expression of mRNAs specific for the predominant myelin-specific proteins. The absolute amounts of CGT message in sciatic nerve and brain were found to be comparable to those that encode the structural proteins of myelin. Except for low amounts in the kidney, the CGT mRNA was not detected in other tissues examined. Southern blot analysis revealed that the CGT protein is likely encoded by a single, relatively large gene. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:234 / 242
页数:9
相关论文
共 43 条
[1]  
Agranoff Bernard W., 1994, P97
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   REVERSIBLE INHIBITION OF OLIGODENDROCYTE PROGENITOR DIFFERENTIATION BY A MONOCLONAL-ANTIBODY AGAINST SURFACE GALACTOLIPIDS [J].
BANSAL, R ;
PFEIFFER, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (16) :6181-6185
[4]  
BENJAMINS JA, 1990, ANN NY ACAD SCI, V605, P90
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]  
COSTANTI.E, 1973, J BIOL CHEM, V248, P8240
[7]   REGULATION OF UDP-GALACTOSE - CERAMIDE GALACTOSYLTRANSFERASE AND UDP-GLUCOSE - CERAMIDE GLUCOSYLTRANSFERASE AFTER CRUSH AND TRANSECTION NERVE INJURY [J].
COSTANTINOCECCARINI, E ;
PODUSLO, JF .
JOURNAL OF NEUROCHEMISTRY, 1989, 53 (01) :205-211
[8]  
DELEON M, 1991, J NEUROSCI RES, V29, P437
[9]   ANTISERUM INDUCED MYELINATION INHIBITION INVITRO WITHOUT COMPLEMENT [J].
DORFMAN, SH ;
FRY, JM ;
SILBERBERG, DH .
BRAIN RESEARCH, 1979, 177 (01) :105-114
[10]  
DYER CA, 1988, J NEUROSCI, V8, P4307