PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13

被引:52
作者
Matthijs, G
Schollen, E
Pirard, M
Budarf, ML
VanSchaftingen, E
Cassiman, JJ
机构
[1] UNIV LOUVAIN,BRUSSELS,BELGIUM
[2] ICP,PHYSIOL CHEM LAB,BRUSSELS,BELGIUM
[3] UNIV PENN,CHILDRENS HOSP PHILADELPHIA,SCH MED,DIV HUMAN GENET & MOL BIOL,PHILADELPHIA,PA 19104
[4] UNIV PENN,DEPT PEDIAT,SCH MED,PHILADELPHIA,PA 19104
关键词
D O I
10.1006/geno.1996.4536
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have cloned the human homologue of SEC53 or yeast phosphomannomutase (HGMW-approved symbol PMM1) from a liver cDNA library, This cDNA encodes a protein of 262 amino acids with a predicted molecular mass of 29 kDa and 54% identity with yeast phosphomannomutase, Expression of the human cDNA in Escherichia coli yielded an active phosphomannomutase, which was purified to homogeneity. Northern blot analysis of human tissues showed strong expression in liver, heart, brain, and pancreas and a lower expression in skeletal muscle, The gene was assigned to chromosome 22113.1 by the use of hybrid cell lines and by fluorescence in situ hybridization. Most patients presenting with carbohydrate-deficient glycoprotein syndrome type 1 (CDG1 or Jaeken disease) have a greatly reduced phosphomannomutase activity; the gene encoding this enzyme is a likely candidate for CDG1 Since the CDG1 locus maps elsewhere in the genome (16p13), mutations in the phosphomannomutase gene encoded by chromosome 22 are not a major cause of CDG1. (C) 1997 Academic Press.
引用
收藏
页码:41 / 47
页数:7
相关论文
共 19 条
[1]   A FAMILY OF HEXOSEPHOSPHATE MUTASES IN SACCHAROMYCES-CEREVISIAE [J].
BOLES, E ;
LIEBETRAU, W ;
HOFMANN, M ;
ZIMMERMANN, FK .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 220 (01) :83-96
[2]   Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panel [J].
Budarf, ML ;
Eckman, B ;
Michaud, D ;
McDonald, T ;
Gavigan, S ;
Buetow, KH ;
Tatsumura, Y ;
Liu, ZG ;
Hilliard, C ;
Driscoll, D ;
Goldmuntz, E ;
Meese, E ;
Zwarthoff, EC ;
Williams, S ;
McDermid, H ;
Dumanski, JP ;
Biegel, J ;
Bell, CJ ;
Emanuel, BS .
GENOMICS, 1996, 35 (02) :275-288
[3]   THE SYNTHESIS OF MANNOSE 1-PHOSPHATE IN BRAIN [J].
GUHA, SK ;
ROSE, ZB .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 243 (01) :168-173
[4]   FAMILIAL PSYCHOMOTOR RETARDATION WITH MARKEDLY FLUCTUATING SERUM PROLACTIN, FSH AND GH LEVELS, PARTIAL TBG-DEFICIENCY, INCREASED SERUM ARYLSULFATASE-A AND INCREASED CSF PROTEIN - NEW SYNDROME [J].
JAEKEN, J ;
VANDERSCHUERENLODEWEYCKX, M ;
CASAER, P ;
SNOECK, L ;
CORBEEL, L ;
EGGERMONT, E ;
EECKELS, R .
PEDIATRIC RESEARCH, 1980, 14 (02) :179-179
[5]   THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROMES - AN OVERVIEW [J].
JAEKEN, J ;
CARCHON, H .
JOURNAL OF INHERITED METABOLIC DISEASE, 1993, 16 (05) :813-820
[6]  
JAEKEN J, 1996, IN PRESS J MED GENET
[7]  
KEPES F, 1988, J BIOL CHEM, V263, P9155
[8]  
KOPLIN R, 1992, J BACTERIOL, V174, P191
[9]  
LANGE AJ, 1993, J BIOL CHEM, V268, P8078
[10]  
LOWRY OH, 1969, J BIOL CHEM, V244, P910